Program EffectivenessSWIFTNCT07814261
Implementation Study With Embedded RCT of a Digital System of Parenting Support Within Government Services in South Africa
A study testing Module 1 - Improve My Relationship with My Teen/Child and Module 2 - Keep My Child/Teen Safe and Healthy in people with Program Effectiveness and Program Implementation, run by University of Cape Town at 1 site in South Africa.
Trial summary
ParentText, a WhatsApp-based parenting support programme, is designed as a universal intervention to improve parent-child relationships (module 1) and promote child safety (module 2). The SWIFT study is an explanatory sequential time series design with an embedded randomised controlled trial. Read more about this study
- Who is it for?
- Ages 18 to 99 yearsHealthy volunteers can take part
- Conditions the study is for
- Program Effectiveness, Program Implementation, Parent Child Relationship
- What is being tested?
- Module 1 - Improve My Relationship with My Teen/Child and Module 2 - Keep My Child/Teen Safe and Healthy
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 4,961 participants
- Where
- 1 siteSouth Africa
- Study dates
- 2 Feb 2026to 31 Oct 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 99 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Be an adolescent of a caregiver who has started the 3-month follow-up survey
- Aged 12-17 years old for the surveys and qualitative interviews
- Have received consent from their parent/caregiver to partake in the study
- Are willing to provide informed assent to participate
- Residing in South Africa
- Sufficiently fluent in English, Afrikaans or IsiXhosa
Show all 13Show fewer
- Have successfully enrolled in the study, therefore meets the eligibility criteria of the study (*as mentioned above)
- Have accessed at least one referral
- Have successfully enrolled in the study, therefore meets the eligibility criteria of the study (*as mentioned above)
- Have completed the baseline survey and received access to the programme content
- Have successfully enrolled in the study, therefore meets the eligibility criteria of the study (*as mentioned above)
- Have been assigned to the intervention group receiving the child safety module
- Have completed at least one component of the module
Who cannot join
None listed.
Trial locations and contacts
1 site in 1 country.
South Africa1 site
University of Cape Town (recruitment sites confidential)
Cape Town, Western Cape, 7700
About this study
Official title: Implementing a Digital System of Parenting Support Within Government Services in South Africa: Protocol for a 1) Time Series Trial of ParentText and 2) Randomized Controlled Trial of an Additional Programme Module for Child Safety
ParentText, a WhatsApp-based parenting support programme, is designed as a universal intervention to improve parent-child relationships (module 1) and promote child safety (module 2). The SWIFT study is an explanatory sequential time series design with an embedded randomised controlled trial. The time-series design aims to assess whether a digital parenting support programme, ParentText, can be embedded effectively into the regular services offered by the Department of Health and Wellness in the Western Cape, South Africa, and to explore factors affecting parent engagement. The embedded randomised controlled trial tests whether the second module affects sexual violence reduction against children. Participants include caregivers 18 years and older, living in South Africa, and caring for at least one child aged 2 to 17 years.
The primary outcome measures of the study are both implementation 1): Assessing which of four approaches to advertising the ParentText programme leads to the highest rates of programme uptake, engagement, and completion; and programmatic: Testing the effectiveness of the additional Child Safety Module in 2) - reducing child sexual violence vulnerability, 3) - increasing child sexual violence risk planning and 4) - reducing child sexual violence exposure.
Read more
The secondary outcomes assess changes in programme users' self-reported parenting behaviour in terms of 1) positive involvement, 2) positive parenting, 3) parent mental health, 4) parent support of education, 5) caregiver child/ adolescent communication, 6) online safety, 7) harsh parenting, 8) child or adolescent behavioural problems; and assessing users' experience of the 9) accessibility of the chatbot, 10) acceptability of the chatbot; and 11) adolescents' report of their sexual violence risk and safety planning communication..
In the first period of the time series design, participants will be recruited via posters, which provide a WhatsApp number for the programme, at their local clinic. Once they join, they will be provided with information on the study and be invited to consent to participate. If they consent, they will complete a baseline survey and then be able to move on to the first 5-day module. On consent to the study, participants will be placed randomly into either the group that receives the second module (intervention group) or a control group that will receive the module only after the study is completed. Both the intervention group and the control group receive the one-month and three-month surveys.
In the second, third, and fourth time periods, everything remains the same except the encouragement method. In the first time period, only posters were used for recruitment. Within the second period, one month later, recruitment will be via both posters and additional encouragement from clinic staff. Clinic staff will encourage either verbally or by providing the caregiver with a flyer during their clinic visit. Throughout both these recruitment periods (1) and (2), caregivers who have completed the programme can share it on social media by posting predesigned tiles that include the joining information for the chatbot. Should our ideal sample size (4,000 participants) not be reached through these mechanisms, there will be an additional time period (3-4 weeks; time period three) during which the study team will advertise directly on Facebook. Finally, should our sample size not be reached in this third period, there will be a fourth time period of advertising that offers ZAR50 (approximately USD3) in airtime to those who sign up. This ZAR50 will be provided in sums of: ZAR15 for completing each of the baseline and one-month questionnaires, and ZAR20 for completing the three-month questionnaire.
Once the three-month questionnaires are completed, participants will also be invited to a focus group discussion or telephonic interviews. Participants will be purposively selected from the group of participants who consent to the qualitative data collection phase.
The focus groups will be conducted with participants residing in the Western Cape province, who completed one or both modules, and will discuss topics such as their experience of the ParentText programme, and the encouragement.
For the telephonic interviews, participants will be purposely selected for interviews, looking at a) caregivers' experience of the child safety module, b) reasons for engaging/not engaging with the programme, and c) which referral services they accessed.
Further, adolescents (over the age of 12 years) will be recruited via their caregivers - upon completion of the 3-month survey, parents or legal guardians will be asked to provide consent for the team to contact their adolescent to undertake a telephonic survey and, in some cases, a qualitative interview with them. Teens will complete informed assent.
- Conditions
- Program Effectiveness, Program Implementation, Parent Child Relationship, Caregiver Child Relationship, Parent Education, Parenting Intervention
- Being tested
- Module 1 - Improve My Relationship with My Teen/Child, Module 2 - Keep My Child/Teen Safe and Healthy
- Keywords
- Prevention, Digital Intervention, Parenting, Violence against Children, Sexual Violence Risk, Time Series Design, Randomised Controlled Trial, South Africa, Public Health System, Child Safety, Child Protection, Intervention, Low- and Middle-Income Countries
- Medical subject headings
- Psychological Well-Being
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Module 1 - Improve My Relationship with My Teen/ChildBehavioural
Module 1 aims to improve caregiver-child relationships. The module has 5 daily lessons. The lessons take 10 minutes a day.
The lessons include:
- Spending One-on-One Time with My Child/Teen,
- Giving Praise,
- Creating a Routine for One-On-One Time,
- Noticing Feelings During One-On-One Time,
- Keeping Calm When We Are Stressed
Module 2 - Keep My Child/Teen Safe and HealthyBehavioural
Module 2 aims to promote child safety. The module has 5 daily lessons. The lessons take 10 minutes a day.
The lessons include:
- Community Safety
- Responding to Crises
- Knowing the Basics of Online Safety
- Build Habits and Trust Online
- For children: Teaching Safe Touch or For teens: Prevent Sexual Violence
| Study group | Role | What they receive |
|---|---|---|
| Child Safety Module | Experimental | The experimental group received a five-day module intended to educate parents about keeping their child safe from online and offline sexual violence (in addiion to a foundational relationship strengthening module). Receives: Behavioral: Module 1 - Improve My Relationship with My Teen/Child; Behavioral: Module 2 - Keep My Child/Teen Safe and Healthy |
| Waitlist Control | Other | Those randomized to the waitlist control will be offered the child safety module after all data has been collected (but will still be able to access the same foundational relationship strengthening module as the experimental group). Receives: Behavioral: Module 1 - Improve My Relationship with My Teen/Child |
What is being measured
The primary outcome is the main question the study is designed to answer.
Engagement with the Chatbot
Uptake, engagement, and completion are measured using process data embedded within the chatbot, including programme uptake, frequency of logging in, duration of engagement, and completion rates of assigned content modules.
Measured: Continuously throughout the three-month period that the chatbot is open.
Sexual Violence Vulnerability
Sexual violence vulnerability is assessed using caregiver-reported items from the Global Parenting Initiative, measuring children's and adolescents' exposure to unsafe situations in their communities. The measure includes five items for adolescents and four for children. Caregivers report how often in the past week their child or teen: spent time with untrusted friends; was unsupervised at home or outside (children) or went to taverns or drank with friends (teens); took a lift with someone unknown; or stayed away overnight without the caregiver knowing their whereabouts or returned late. Caregivers of adolescents also report their adolescents receiving sexual comments from older individuals. Responses are coded as (0) Never, (1) Sometimes (1-2 times), or (2) Often (3 or more times), with "I don't know" coded as 777 and "prefer not to say" coded as 888. Scores are summed for a total vulnerability score.
Measured: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete the questionnaire.
Secondary outcomes (16)
Caregiver Positive Involvement
Positive involvement refers to the amount of caregiver participation in games and activities with their child or teen, and is measured using the one item from the positive involvement subscale of the Alabama Parenting Questionnaire (APQ; Essau et al., 2006), namely "How often in the past week did you play games or do other fun activities with your child/teen?" Response items include (0) Never, (1) Sometimes (1-2 times), (2) Often (3 or more times), or "prefer not to say" coded as 888.
Measured: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Positive Parenting
Positive parenting is measured using the one item from the positive parenting subscale of the Alabama Parenting Questionnaire (APQ; Clerkin et al., 2007), namely "How often in the past week did you praise your child/teen when they behaved well?" Response items include (0) Never, (1) Sometimes (1-2 times), (2) Often (3 or more times), or "prefer not to say" coded as 888.
Measured: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Parent Mental Health
Parent mental health is measured using the Patient Health Questionnaire (PHQ-2; Löwe et al., 2005). The PHQ-2 measures depressed mood and anhedonia, and consists of the last two items of the PHQ-4 (Kroenke et al., 2009). The two items include, "How often in the past week have you felt down, depressed, or hopeless?" and "How often in the past week did you have little interest or pleasure in doing things?" The response options for this study range from 0 (Never) to 2 (Often - 3 or more times), with an option for "prefer not to say" coded as 888, to fit the responses of the other measures. The total score is calculated by summing the two responses. The validity of the PHQ-2 has been recognised in South African studies among patients attending primary health facilities (Bhana et al., 2015; Levis et al., 2020). Previous studies indicate that the PHQ-2 has sound reliability, with Cronbach alpha scores ranging from 0.78 to 0.92 (Löwe et al., 2005; Staples et al., 2019; Lee et al., 2026).
Measured: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Caregiver Safety Planning Communication
Safety planning communication is assessed using locally derived items from the Global Parenting Initiative by asking caregivers of a child: "Have you talked to your child in the past week about keeping safe?" Caregivers of teens are presented with two questions: "Have you talked to your teen in the past week about keeping safe in any of these situations?" and "Have you talked to your teen in the past week about keeping safe from situations such as sexual violence?" The safety planning communication questions are presented immediately after the items on sexual violence vulnerability; thus, "any of these situations" refers to the risky situations mentioned on sexual violence vulnerability items. Response items include (0) No, (1) Yes, or "prefer not to say" coded as 888. The sum of the item scores is used to obtain a total score.
Measured: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Caregivers have one week to complete each questionnaire.
Child Sexual Violence Exposure
Sexual violence exposure is assessed in the survey, within the chatbot, using four items for caregivers of children and teens. Caregivers are asked how often their child/teen has been exposed to four instances of sexual violence in the past month. These instances include whether their child/teen displayed inappropriate sexual behaviour, was touched sexually, was shown something sexual, or was made to do anything sexual. These occurrences provided are a combination of sexual violence items retrieved from the Sexual Abuse subscale of the International Society for the Prevention of Child Abuse and Neglect (ISPCAN) Child Abuse Screening Tool-Trial Version (ICAST-T; Meinck et al., 2018). Response items include (0) Never, (1) Sometimes (1-2 times), or (2) Often (3+ times), with "I don't know" coded as 777 and "prefer not to say" coded as 888. The sum of the item scores is used to obtain a total score.
Measured: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Parent Support of Education
Parent support of education is measured using caregiver-reported items from prior research (Ceballo et al., 2014) and applied in Parenting for Lifelong Health (PLH) studies. The scale includes two items each for caregivers of children and adolescents, assessing engagement in education-related activities. Caregivers report how often in the past week they praised their child or teen for working hard at school. Caregivers of teens also report how often they supported their teen's schoolwork, while caregivers of children indicate how often they named, counted, or drew with their child, based on the Family Care Indicators from the UNICEF Multiple Indicator Cluster Survey (Kariger et al., 2012). Responses are coded as (0) Never, (1) Sometimes (1-2 times), or (2) Often (3 or more times), with "prefer not to say" coded as 888. The sum of the item scores is used to obtain a total score.
Measured: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Parents have one week to complete each questionnaire.
Caregiver Child/ Adolescent Communication
This outcome assesses changes in programme users' perceived openness in communication with their children. Caregiver-Child/Adolescent Communication is measured using one item for caregivers of children and two items for caregivers of teens. Caregivers of children and teens are asked, "How often in the past week did your child/teen let you know what is bothering them?", while caregivers of teens are also asked "How often in the past week could you talk about personal things like boyfriends, girlfriends, or sexual behaviour, with Your Teen?". These items are adapted from a subscale of the Parent-Child Communication (PCC) scale, which was used in the Fast Track Intervention Study (McCarty \& Doyle, 2001). Response items include (0) Never, (1) Sometimes (1-2 times), (2) Often (3 or more times), or "prefer not to say" coded as 888.
Measured: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Parents have one week to complete each questionnaire.
Caregiver Monitoring of Child's Online Safety
Online safety assesses programme user changes in their engagement with their children regarding their children's use of the internet and/or mobile devices. It is assessed for caregivers of children and teens using two items, namely "How often in the past week did you know what your child was doing when they were using the internet, cellphone, or other device?" from the the Global Kids Online survey (GKO; 2020) and "How often in the past week did you talk to your child about their use of the internet or device?" from the EU Kids Online Survey (Šmahel et al., 2020). Response items include (0) Never, (1) Sometimes (1-2 times), (2) Often (3 or more times), or "prefer not to say" coded as 888. Sores on the items are summed to obtain a total score for online safety.
Measured: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Caregiver Involvement
Caregiver involvement is assessed with three items from the Family Care Indicators (FCI) subscale of the UNICEF Multiple Indicator Cluster Survey (MICS; Kariger et al., 2012). Caregiver involvement items assess caregivers' perceptions of their involvement with their children, including active participation in activities and decision-making processes. The three items ask how often in the past week a caregiver actively participated in activities with their child/teen, such as playing, sharing books, or helping with homework; were involved in making decisions regarding their child/teen's education, health, and overall well-being; and showed their child/teen affection or love. Response items include (0) Never, (1) Sometimes (1-2 times), (2) Often (3 or more times), or "prefer not to say" coded as 888. The three items will be summed to create a total score.
Measured: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Other Caregiver Involvement
If applicable, the caregiver completing the programme also responds to similar items to those they completed for themselves, reflecting their perspective on another caregiver's involvement in their child's life. Other caregiver involvement is assessed with three items from the Family Care Indicators (FCI) subscale of the UNICEF Multiple Indicator Cluster Survey (MICS; Kariger et al., 2012). The three items include how often the other caregiver actively participated in activities with the child/teen, such as playing, sharing books, or helping with homework; was involved in making decisions regarding the child/teen's education, health, and overall well-being; and showed the child/teen affection or love. Response items include (0) Never, (1) Sometimes (1-2 times), (2) Often (3 or more times), or "prefer not to say" coded as 888. The three items will be summed to create a total score.
Measured: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Harsh Parenting
To assess programme user changes in harsh parenting, items adapted from the physical abuse (1 item) and emotional abuse (1 item) subscales of the International Society for the Prevention of Child Abuse and Neglect (ISPCAN) Child Abuse Screening Tool-Trial Version (ICAST-T; Meinck et al., 2018) are used. These items measure caregivers' behaviours towards their children, indicative of maltreatment. The two items include: "How often in the past week did you discipline your child/teen physically, such as hitting with your hand, belt, or another object?" (physical abuse) and "How often in the past week did you shout or scream at your child/teen?" (emotional abuse). Response items include (0) Never, (1) Sometimes (1-2 times), (2) Often (3 or more times), or "prefer not to say" coded as 888. The sum of the item scores is used to obtain an overall score for harsh parenting.
Measured: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Child or Adolescent Behavioural Problems
This outcome assesses whether programme users report changes in their child or adolescent's behavioural problems (externalising symptoms). Child or Adolescent Behavioural Problems are measured using one item, namely "How often in the past week did your child/teen not obey, or it was difficult to make them obey?" from the Child and Adolescent Behaviour Inventory (CABI; Cianchetti et al., 2013), which assesses caregivers' perceptions of externalising behaviours in their children (Cianchetti et al., 2013). Response items include (0) Never, (1) Sometimes (1-2 times), (2) Often (3 or more times), or "prefer not to say" coded as 888.
Measured: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Chatbot Accessibility
The accessibility of the ParentText programme will be measured using a single question embedded in the chatbot: "What did you mainly use to connect to ParentText?" with response options (0) "Mobile data", (1) "WiFi at home", (2) "WiFi at work", (3) "Hotspot in the community", (4) "Other", or "prefer not to say" coded as 888.
Measured: 1 month post-baseline; participants have one week to complete the questionnaire.
Chatbot Acceptability
The acceptability of the ParentText programme will be measured using the following question embedded in the chatbot: "How helpful was ParentText to you and your family?" with response options (0) "Not helpful", (1) "A bit helpful", (2) "Very helpful", or "prefer not to say" coded as 888.
Measured: 1-month post-baseline; participants have one week to complete the questionnaire.
Adolescent Report of Sexual Violence Vulnerability
This outcome aims to assess adolescent-reported sexual violence vulnerability via a brief individual telephonic survey. Adolescents' sexual violence vulnerability is measured with the questions: In the past week (7 days), how often: Did you spend time with friends that your parent doesn't know or doesn't trust? Did you go to a tavern or drink alcohol with your friends? Were you out of the house at night alone, or your parent didn't know where you were, or you came home later than your parent expected? Did you get a lift in a car with someone you don't know? Did you receive sexual comments from men or women who are older than you? Did your parent know what you were doing when you were using the internet or using the cell phone? Item responses include (0) Never, (1) Sometimes (1-2 times), (2) Often (3 or more times), or "prefer not to say/skip" coded as 888. Item responses are summed to compute a total score.
Measured: After completion of 3-month post-baseline survey, we will have a 3-month window in which to collect this data.
Adolescents' Report of their Safety Planning Communication (Risk Planning)
Questions include: In the past week (7 days), did your parent talk to you about: Spending time with friends that they don't know or trust? Going to a tavern or drinking alcohol with friends? Being out of the house at night alone, or somewhere where they didn't know where you were, or about coming home later than your parent expected? Getting a lift in a car with someone you don't know? Receiving sexual comments from men or women who are older than you? Keeping safe from situations such as sexual violence? Responses to these items are coded as (0) No, (1) Yes, or "prefer not to say/skip" coded as 888. In the past week (7 days): How often could you talk to your parent about personal things like boyfriends, girlfriends, or sexual behaviour? How often did your parent talk to you about using your cell phone or being on the internet? These two items are coded as (0) Never, (1) Sometimes (1-2 times), (2) Often (3 or more times), or "prefer not to say/skip" coded as 888.
Measured: After completion of 3-month post-baseline survey, over a three-month data collection window.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Sep 2026
- Study start2 Feb 2026
- Primary completion31 Oct 2026 (estimated)
- Study completion31 Oct 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (13)Papers the sponsor has linked to this study.
- Other trials for Program EffectivenessStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Sequential
- Model description
- This study will adopt an explanatory sequential model (Creswell \& Creswell, 2017). The quantitative phase employs a time series design with an embedded randomised controlled trial. Quantitative data collection will be gathered using surveys and process data (both collected within the chatbot). The results of the quantitative data will be used to inform the groups who will be qualitatively interviewed and the questions asked of them. Although tentatively designed, the qualitative interviews will explore results from the quantitative surveys. Focus groups and interviews (telephonic and in-person) will be conducted with caregivers, their adolescents, and clinic staff.
- Masking
- None (open label)
- Enrolment
- 4,961 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Cape Town
- Sponsor type
- University, hospital or other
- Collaborators
- University of Oxford, UNICEF, LEGO Foundation, Oak Foundation, Parenting for Lifelong Health, IDEMS International, Clowns Without Borders South Africa, City of Cape Town, Western Cape Department of Health and Wellness, Childline, South African Parenting Programme Implementers Network
- Responsible party
- Principal investigator, Dr Catherine L. Ward, University of Cape Town
- Investigators
- Catherine L Ward, PhD, Principal investigator, University of Cape Town
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07814261
- Sponsor's protocol ID
- SWIFT_study
- Acronym
- SWIFT
- Status last verified
- Aug 2026
- First submitted
- 26 Aug 2026
- Last updated
- 10 Sep 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: The quantitative (chatbot survey and adolescent telephonic survey) data will be deidentified and published on UCT's open access portal, ZivaHub. Qualitative data will not be published due to deductive disclosure.
Publications
Šmahel, D., Macháčková, H., Mascheroni, G., Dědková, L., Staksrud, E., Ólafsson, K., Livingstone, S., & Hasebrink, U. (2020). EU Kids Online 2020: Survey results from 19 countries. https://researchonline.lse.ac.uk/id/eprint/103294/1/EU_Kids_Online_2020_March2020.pdf
Kariger P, Frongillo EA, Engle P, Britto PM, Sywulka SM, Menon P. Indicators of family care for development for use in multicountry surveys. J Health Popul Nutr. 2012 Dec;30(4):472-86. doi: 10.3329/jhpn.v30i4.13417.
PubMed 23304914Bhana A, Rathod SD, Selohilwe O, Kathree T, Petersen I. The validity of the Patient Health Questionnaire for screening depression in chronic care patients in primary health care in South Africa. BMC Psychiatry. 2015 May 23;15:118. doi: 10.1186/s12888-015-0503-0.
PubMed 26001915Cianchetti C, Pittau A, Carta V, Campus G, Littarru R, Ledda MG, Zuddas A, Fancello GS. Child and Adolescent Behavior Inventory (CABI): A New Instrument for Epidemiological Studies and Pre-Clinical Evaluation. Clin Pract Epidemiol Ment Health. 2013;9:51-61. doi: 10.2174/1745017901309010051. Epub 2013 Feb 22.
PubMed 23539369Creswell, J. W., & Creswell, J. D. (2017). Chapter 10: Mixed methods procedures. In Research design: Qualitative, quantitative, and mixed methods approaches (5th ed., pp. 213-246). SAGE Publications.
Lee GY, Latimer MC, Kelly SM, Verinumbe T, Agee T, Hutton H, Lesko C, Jones J, Schwartz S, Hsu J, Falade-Nwulia O. Utility of the brief Patient Health Questionnaire-2 and Generalized Anxiety Disorder-2 screeners for depression and generalized anxiety symptom identification in people with human immunodeficiency virus. HIV Res Clin Pract. 2026 Dec 31;27(1):2616103. doi: 10.1080/25787489.2026.2616103. Epub 2026 Jan 21.
PubMed 41566210Staples LG, Dear BF, Gandy M, Fogliati V, Fogliati R, Karin E, Nielssen O, Titov N. Psychometric properties and clinical utility of brief measures of depression, anxiety, and general distress: The PHQ-2, GAD-2, and K-6. Gen Hosp Psychiatry. 2019 Jan-Feb;56:13-18. doi: 10.1016/j.genhosppsych.2018.11.003. Epub 2018 Nov 22.
PubMed 30508772Kroenke K, Spitzer RL, Williams JB, Lowe B. An ultra-brief screening scale for anxiety and depression: the PHQ-4. Psychosomatics. 2009 Nov-Dec;50(6):613-21. doi: 10.1176/appi.psy.50.6.613.
PubMed 19996233Lowe B, Kroenke K, Grafe K. Detecting and monitoring depression with a two-item questionnaire (PHQ-2). J Psychosom Res. 2005 Feb;58(2):163-71. doi: 10.1016/j.jpsychores.2004.09.006.
PubMed 15820844Meinck F, Boyes ME, Cluver L, Ward CL, Schmidt P, DeStone S, Dunne MP. Adaptation and psychometric properties of the ISPCAN Child Abuse Screening Tool for use in trials (ICAST-Trial) among South African adolescents and their primary caregivers. Child Abuse Negl. 2018 Aug;82:45-58. doi: 10.1016/j.chiabu.2018.05.022. Epub 2018 May 31.
PubMed 29860107McCarty, C.M., & Doyle, S.R. (2001). Parent-Child Communication (Child) (Technical Report). http://www.fasttrackproject.org/
Ceballo R, Maurizi LK, Suarez GA, Aretakis MT. Gift and sacrifice: parental involvement in Latino adolescents' education. Cultur Divers Ethnic Minor Psychol. 2014 Jan;20(1):116-27. doi: 10.1037/a0033472. Epub 2013 Jul 8.
PubMed 23834259Clerkin SM, Marks DJ, Policaro KL, Halperin JM. Psychometric properties of the Alabama parenting questionnaire-preschool revision. J Clin Child Adolesc Psychol. 2007 Mar;36(1):19-28. doi: 10.1080/15374410709336565.
PubMed 17206878
Study at a glance
From the registry record, last updated by the sponsor on 10 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Implementing a Digital System of Parenting Support Within Government Services in South Africa: Protocol for a 1) Time Series Trial of ParentText and 2) Randomized Controlled Trial of an Additional Programme Module for Child Safety
- ClinicalTrials.gov ID
- NCT07814261
- Acronym / sponsor ID
- SWIFT / SWIFT_study
- Conditions
- Program Effectiveness, Program Implementation, Parent Child Relationship, Caregiver Child Relationship, Parent Education, Parenting Intervention
- Keywords
- Prevention, Digital Intervention, Parenting, Violence against Children, Sexual Violence Risk, Time Series Design, Randomised Controlled Trial, South Africa
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 4,961 participants (actual)
- Lead sponsor
- University of Cape TownUniversity, hospital or other
- Collaborators
- University of Oxford, UNICEF, LEGO Foundation, Oak Foundation, Parenting for Lifelong Health, IDEMS International, Clowns Without Borders South Africa, City of Cape Town, Western Cape Department of Health and Wellness, Childline, South African Parenting Programme Implementers Network
- Study start
- 2 Feb 2026 (actual)
- Primary completion
- 31 Oct 2026 (estimated)
- Study completion
- 31 Oct 2026 (estimated)
- First posted
- 10 Sep 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
ParentText, a WhatsApp-based parenting support programme, is designed as a universal intervention to improve parent-child relationships (module 1) and promote child safety (module 2). The SWIFT study is an explanatory sequential time series design with an embedded randomised controlled trial. The time-series design aims to assess whether a digital parenting support programme, ParentText, can be embedded effectively into the regular services offered by the Department of Health and Wellness in the Western Cape, South Africa, and to explore factors affecting parent engagement. The embedded randomised controlled trial tests whether the second module affects sexual violence reduction against children. Participants include caregivers 18 years and older, living in South Africa, and caring for at least one child aged 2 to 17 years.
The primary outcome measures of the study are both implementation 1): Assessing which of four approaches to advertising the ParentText programme leads to the highest rates of programme uptake, engagement, and completion; and programmatic: Testing the effectiveness of the additional Child Safety Module in 2) - reducing child sexual violence vulnerability, 3) - increasing child sexual violence risk planning and 4) - reducing child sexual violence exposure.
The secondary outcomes assess changes in programme users' self-reported parenting behaviour in terms of 1) positive involvement, 2) positive parenting, 3) parent mental health, 4) parent support of education, 5) caregiver child/ adolescent communication, 6) online safety, 7) harsh parenting, 8) child or adolescent behavioural problems; and assessing users' experience of the 9) accessibility of the chatbot, 10) acceptability of the chatbot; and 11) adolescents' report of their sexual violence risk and safety planning communication..
In the first period of the time series design, participants will be recruited via posters, which provide a WhatsApp number for the programme, at their local clinic. Once they join, they will be provided with information on the study and be invited to consent to participate. If they consent, they will complete a baseline survey and then be able to move on to the first 5-day module. On consent to the study, participants will be placed randomly into either the group that receives the second module (intervention group) or a control group that will receive the module only after the study is completed. Both the intervention group and the control group receive the one-month and three-month surveys.
In the second, third, and fourth time periods, everything remains the same except the encouragement method. In the first time period, only posters were used for recruitment. Within the second period, one month later, recruitment will be via both posters and additional encouragement from clinic staff. Clinic staff will encourage either verbally or by providing the caregiver with a flyer during their clinic visit. Throughout both these recruitment periods (1) and (2), caregivers who have completed the programme can share it on social media by posting predesigned tiles that include the joining information for the chatbot. Should our ideal sample size (4,000 participants) not be reached through these mechanisms, there will be an additional time period (3-4 weeks; time period three) during which the study team will advertise directly on Facebook. Finally, should our sample size not be reached in this third period, there will be a fourth time period of advertising that offers ZAR50 (approximately USD3) in airtime to those who sign up. This ZAR50 will be provided in sums of: ZAR15 for completing each of the baseline and one-month questionnaires, and ZAR20 for completing the three-month questionnaire.
Once the three-month questionnaires are completed, participants will also be invited to a focus group discussion or telephonic interviews. Participants will be purposively selected from the group of participants who consent to the qualitative data collection phase.
The focus groups will be conducted with participants residing in the Western Cape province, who completed one or both modules, and will discuss topics such as their experience of the ParentText programme, and the encouragement.
For the telephonic interviews, participants will be purposely selected for interviews, looking at a) caregivers' experience of the child safety module, b) reasons for engaging/not engaging with the programme, and c) which referral services they accessed.
Further, adolescents (over the age of 12 years) will be recruited via their caregivers - upon completion of the 3-month survey, parents or legal guardians will be asked to provide consent for the team to contact their adolescent to undertake a telephonic survey and, in some cases, a qualitative interview with them. Teens will complete informed assent.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Sequential
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- This study will adopt an explanatory sequential model (Creswell \& Creswell, 2017). The quantitative phase employs a time series design with an embedded randomised controlled trial. Quantitative data collection will be gathered using surveys and process data (both collected within the chatbot). The results of the quantitative data will be used to inform the groups who will be qualitatively interviewed and the questions asked of them. Although tentatively designed, the qualitative interviews will explore results from the quantitative surveys. Focus groups and interviews (telephonic and in-person) will be conducted with caregivers, their adolescents, and clinic staff.
| Arm | Type | Receives |
|---|---|---|
| Child Safety Module | Experimental | Behavioral: Module 1 - Improve My Relationship with My Teen/Child, Behavioral: Module 2 - Keep My Child/Teen Safe and HealthyThe experimental group received a five-day module intended to educate parents about keeping their child safe from online and offline sexual violence (in addiion to a foundational relationship strengthening module). |
| Waitlist Control | Other | Behavioral: Module 1 - Improve My Relationship with My Teen/ChildThose randomized to the waitlist control will be offered the child safety module after all data has been collected (but will still be able to access the same foundational relationship strengthening module as the experimental group). |
Who may qualify
- Ages
- 18 to 99 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (13 listed)
- Be an adolescent of a caregiver who has started the 3-month follow-up survey
- Aged 12-17 years old for the surveys and qualitative interviews
- Have received consent from their parent/caregiver to partake in the study
- Are willing to provide informed assent to participate
- Residing in South Africa
Key exclusion criteria (0 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Module 1 - Improve My Relationship with My Teen/ChildModule 1 aims to improve caregiver-child relationships. The module has 5 daily lessons. The lessons take 10 minutes a day. The lessons include: 1. Spending One-on-One Time with My Child/Teen, 2. Giving Praise, 3. Creating a Routine for One-On-One Time, 4. Noticing Feelings During One-On-One Time, 5. Keeping Calm When We Are Stressed | Behavioural | Child Safety Module, Waitlist Control |
| Module 2 - Keep My Child/Teen Safe and HealthyModule 2 aims to promote child safety. The module has 5 daily lessons. The lessons take 10 minutes a day. The lessons include: 1. Community Safety 2. Responding to Crises 3. Knowing the Basics of Online Safety 4. Build Habits and Trust Online 5. For children: Teaching Safe Touch or For teens: Prevent Sexual Violence | Behavioural | Child Safety Module |
Primary outcome
Engagement with the Chatbot
Time frame: Continuously throughout the three-month period that the chatbot is open.
Uptake, engagement, and completion are measured using process data embedded within the chatbot, including programme uptake, frequency of logging in, duration of engagement, and completion rates of assigned content modules.
Sexual Violence Vulnerability
Time frame: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete the questionnaire.
Sexual violence vulnerability is assessed using caregiver-reported items from the Global Parenting Initiative, measuring children's and adolescents' exposure to unsafe situations in their communities. The measure includes five items for adolescents and four for children. Caregivers report how often in the past week their child or teen: spent time with untrusted friends; was unsupervised at home or outside (children) or went to taverns or drank with friends (teens); took a lift with someone unknown; or stayed away overnight without the caregiver knowing their whereabouts or returned late. Caregivers of adolescents also report their adolescents receiving sexual comments from older individuals. Responses are coded as (0) Never, (1) Sometimes (1-2 times), or (2) Often (3 or more times), with "I don't know" coded as 777 and "prefer not to say" coded as 888. Scores are summed for a total vulnerability score.
16 secondary outcomes
Caregiver Positive Involvement
Time frame: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Positive Parenting
Time frame: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Parent Mental Health
Time frame: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Caregiver Safety Planning Communication
Time frame: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Caregivers have one week to complete each questionnaire.
Child Sexual Violence Exposure
Time frame: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Parent Support of Education
Time frame: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Parents have one week to complete each questionnaire.
Caregiver Child/ Adolescent Communication
Time frame: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Parents have one week to complete each questionnaire.
Caregiver Monitoring of Child's Online Safety
Time frame: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Caregiver Involvement
Time frame: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Other Caregiver Involvement
Time frame: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Harsh Parenting
Time frame: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Child or Adolescent Behavioural Problems
Time frame: Baseline pre-intervention, 1 month post-baseline, 3 months post-baseline. Participants have one week to complete each questionnaire.
Chatbot Accessibility
Time frame: 1 month post-baseline; participants have one week to complete the questionnaire.
Chatbot Acceptability
Time frame: 1-month post-baseline; participants have one week to complete the questionnaire.
Adolescent Report of Sexual Violence Vulnerability
Time frame: After completion of 3-month post-baseline survey, we will have a 3-month window in which to collect this data.
Adolescents' Report of their Safety Planning Communication (Risk Planning)
Time frame: After completion of 3-month post-baseline survey, over a three-month data collection window.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Sep 2026.
- BackgroundŠmahel, D., Macháčková, H., Mascheroni, G., Dědková, L., Staksrud, E., Ólafsson, K., Livingstone, S., & Hasebrink, U. (2020). EU Kids Online 2020: Survey results from 19 countries. https://researchonline.lse.ac.uk/id/eprint/103294/1/EU_Kids_Online_2020_March2020.pdf
- Background: PubMed 23304914Kariger P, Frongillo EA, Engle P, Britto PM, Sywulka SM, Menon P. Indicators of family care for development for use in multicountry surveys. J Health Popul Nutr. 2012 Dec;30(4):472-86. doi: 10.3329/jhpn.v30i4.13417.
- Background: PubMed 26001915Bhana A, Rathod SD, Selohilwe O, Kathree T, Petersen I. The validity of the Patient Health Questionnaire for screening depression in chronic care patients in primary health care in South Africa. BMC Psychiatry. 2015 May 23;15:118. doi: 10.1186/s12888-015-0503-0.
- Background: PubMed 23539369Cianchetti C, Pittau A, Carta V, Campus G, Littarru R, Ledda MG, Zuddas A, Fancello GS. Child and Adolescent Behavior Inventory (CABI): A New Instrument for Epidemiological Studies and Pre-Clinical Evaluation. Clin Pract Epidemiol Ment Health. 2013;9:51-61. doi: 10.2174/1745017901309010051. Epub 2013 Feb 22.
- BackgroundCreswell, J. W., & Creswell, J. D. (2017). Chapter 10: Mixed methods procedures. In Research design: Qualitative, quantitative, and mixed methods approaches (5th ed., pp. 213-246). SAGE Publications.
- Background: PubMed 41566210Lee GY, Latimer MC, Kelly SM, Verinumbe T, Agee T, Hutton H, Lesko C, Jones J, Schwartz S, Hsu J, Falade-Nwulia O. Utility of the brief Patient Health Questionnaire-2 and Generalized Anxiety Disorder-2 screeners for depression and generalized anxiety symptom identification in people with human immunodeficiency virus. HIV Res Clin Pract. 2026 Dec 31;27(1):2616103. doi: 10.1080/25787489.2026.2616103. Epub 2026 Jan 21.
- Background: PubMed 30508772Staples LG, Dear BF, Gandy M, Fogliati V, Fogliati R, Karin E, Nielssen O, Titov N. Psychometric properties and clinical utility of brief measures of depression, anxiety, and general distress: The PHQ-2, GAD-2, and K-6. Gen Hosp Psychiatry. 2019 Jan-Feb;56:13-18. doi: 10.1016/j.genhosppsych.2018.11.003. Epub 2018 Nov 22.
- Background: PubMed 19996233Kroenke K, Spitzer RL, Williams JB, Lowe B. An ultra-brief screening scale for anxiety and depression: the PHQ-4. Psychosomatics. 2009 Nov-Dec;50(6):613-21. doi: 10.1176/appi.psy.50.6.613.
- Background: PubMed 15820844Lowe B, Kroenke K, Grafe K. Detecting and monitoring depression with a two-item questionnaire (PHQ-2). J Psychosom Res. 2005 Feb;58(2):163-71. doi: 10.1016/j.jpsychores.2004.09.006.
- Background: PubMed 29860107Meinck F, Boyes ME, Cluver L, Ward CL, Schmidt P, DeStone S, Dunne MP. Adaptation and psychometric properties of the ISPCAN Child Abuse Screening Tool for use in trials (ICAST-Trial) among South African adolescents and their primary caregivers. Child Abuse Negl. 2018 Aug;82:45-58. doi: 10.1016/j.chiabu.2018.05.022. Epub 2018 May 31.
- BackgroundMcCarty, C.M., & Doyle, S.R. (2001). Parent-Child Communication (Child) (Technical Report). http://www.fasttrackproject.org/
- Background: PubMed 23834259Ceballo R, Maurizi LK, Suarez GA, Aretakis MT. Gift and sacrifice: parental involvement in Latino adolescents' education. Cultur Divers Ethnic Minor Psychol. 2014 Jan;20(1):116-27. doi: 10.1037/a0033472. Epub 2013 Jul 8.
- Related InfoLink provided by the sponsor.
- Individual participant dataSharing planned: Yes. The quantitative (chatbot survey and adolescent telephonic survey) data will be deidentified and published on UCT's open access portal, ZivaHub. Qualitative data will not be published due to deductive disclosure.
Related trials for Program Effectiveness
Recruiting
The Efficacy of an IADL-based Non-immersive Virtual Reality Training Program to Enhance ADL Performance and Cognitive Function for Persons at Risk of Dementia
Cognitive Enhancement, Subjective Cognitive Decline (SCD)
Not yet recruiting
Effectiveness Of Project EX: A Classroom-Based Smoking Prevention And Cessation Intervention Program
Focus of the Study is Smoking Cessation and Prevention, Smoking Prevention
Recruiting
Effects of a Community-based Multicomponent Physical Exercise Program on Physical Function, Frailty, and Sarcopenia in Older Adults From the Municipality of Santoña: a Quasi-experimental Study.
Frailty/Sarcopenia, Frailty in Older Adults
RecruitingPhase 3
A Study to Evaluate the Efficacy and Safety of Tulisokibart (MK-7240) in Participants With Moderate to Severe Crohn's Disease (MK-7240-008)
Crohn's Disease
Recruiting
Efficacy of the MAEva Program (Meditation, Acceptance, and Commitment to Values) Among Patients Treated For Breast Cancer.
Non Metastatic Breast Cancer
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Catherine L Ward, PhD principal investigator
University of Cape Town
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Module 1 - Improve My Relationship with My Teen/Child and Module 2 - Keep My Child/Teen Safe and Healthy in people with Program Effectiveness and Program Implementation, run by University of Cape Town at 1 site in South Africa.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 13 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 10 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in South Africa. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Engagement with the Chatbot (time frame: Continuously throughout the three-month period that the chatbot is open.). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07814261, which also lists 13 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Sep 2026.