Parent Child AbuseNCT03539341
Parenting for Lifelong Health - Thailand
A study testing PLH-Thailand parenting programme in people with Parent Child Abuse and Domestic Violence, run by University of Oxford at 4 sites in Thailand.
Trial summary
Pilot design: The feasibility pilot of PLH for Young Children in Thailand has a single-site, pre-post design with no control group, with the aims of assessing programme implementation, cultural and contextual relevance, and study feasibility. Read more about this study
- Who is it for?
- Ages 2 years and olderHealthy volunteers can take part
- Conditions the study is for
- Parent Child Abuse, Domestic Violence, Child Behavior Problem
- What is being tested?
- PLH-Thailand parenting programme
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 120 participants
- Where
- 4 sitesThailand
- Study dates
- 11 Dec 2018to 1 Feb 2020
- Phase
- Interventional
- Are there results?
- None posted in the registry
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 2 years and older
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Adult inclusion criteria:
- Men or women aged 18 or older;
- Serves as the primary caregiver of a child in the household between the ages of 2 and 9;
- Parent passes the screening interview, based on the Multiple Indicator Cluster Survey (MICS) version 6 module on child discipline;
- Provides consent to participate in the full study; and
- Agrees to participate in the PLH for Young Children Thailand parenting programme.
Child inclusion criteria:
- Aged 2 to 9 years; and
- Parent/primary caregiver meets the above inclusion criteria.
Inclusion criteria for programme facilitators, who will deliver the PLH for Young Children Thailand programme:
- Age 18 or older;
- Prior participation in a five-day facilitator training workshop provided by PLH Trainers; and
- Agreement to deliver the entire eight session PLH for Young Children Thailand programme.
Adult exclusion criteria:
- Any adult exhibiting severe mental health problems or acute mental disabilities;
- Any adult who is unavailable for participation in the PLH for Young Children Thailand programme at time of recruitment;
- Any adult who has already participated in the feasibility pilot.
Child exclusion criteria:
Any child exhibiting acute physical or mental disabilities.
Trial locations and contacts
4 sites in 1 country.
Thailand4 sites
Ban Tat Health Promotion Hospital
Udon Thani, 41000
Chiang Pin Health Promotion Hospital
Udon Thani, 41000
Kling Kam Health Promotion Hospital
Udon Thani, 41000
Na Phu Health Promotion Hospital
Udon Thani, 41000
About this study
Official title: Randomized Controlled Trial of an Evidence-informed Parenting Intervention to Prevent Violence Against Young Children by Parents and Primary Caregivers in Thailand
Pilot design:
The feasibility pilot of PLH for Young Children in Thailand has a single-site, pre-post design with no control group, with the aims of assessing programme implementation, cultural and contextual relevance, and study feasibility. Although there is no comparison group and it is not designed to test effects, the pilot also has a provisional goal of reductions in child physical and emotional abuse at one-month post-intervention.
Read more
RCT design:
The RCT of PLH for Young Children Thailand is a randomized, controlled, observer-blinded, single-site trial with two parallel groups and a primary endpoint goal of reductions in child physical and emotional abuse at one month and three-months post-intervention. Randomisation will be performed at the individual level with a 1:1 allocation ratio.
Allocation: Using a 1:1 allocation ratio, the 120 participants will be randomly assigned to either the intervention or control group using the concealed computerized programme Sealed Envelope. An external researcher based at the Department of Social Policy and Intervention at the University of Oxford, and who is not directly involved in the study, will generate the random sequence. The Project Coordinator and Co-Investigator McCoy will notify participants of their allocation status via telephone following the collection of baseline data, in order to ensure that participants remain blind to their status during the initial assessment.
Blinding: Due to the involvement of facilitators and coaches in the delivery of the programme, blinding will not be possible for deliverers; moreover, participants cannot be blinded to their allocation status following the initial assessment. However, the allocation status of other participants will be kept concealed from participants in order to reduce the risk of contamination. Data collectors gathering outcome and process evaluation data, as well as statisticians providing support in data analysis, will be blinded to participant allocation status for the purposes of minimizing assessment bias. Cases of compromised blinding will be immediately reported to the Research Manager, who will consult with the research team on an appropriate course of action. Un-blinding of participants will only be permitted if any instances of significant harm due to participation in the study are reported by a participant or any member of the project team at any stage of the study.
This study is funded by the United Nations Children's Fund (UNICEF) Thailand and the Department of Social Policy and Intervention, University of Oxford.
UNICEF grant reference: PCA/THLC/2017/002
- Conditions
- Parent Child Abuse, Domestic Violence, Child Behavior Problem, Child Neglect, Depression, Anxiety, Parent-Child Relations
- Being tested
- PLH-Thailand parenting programme, Control (care as usual)
- Medical subject headings
- Depression, Anxiety Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PLH-Thailand parenting programmeBehavioural
Parenting programmes include developing positive caregiver-child interaction through child-led play and emotional communication, praise and rewards to encourage positive child behaviour, limit-setting behaviours such as effective instruction giving and establishing consistent household rules, and non-violent discipline strategies to replace harsh parenting and corporal punishment.
Control (care as usual)Other
The control will be an inactive condition of standard care at the time of the intervention. 'Standard care' may include access to Parent Schools in Mother and Child Health clinics at public hospitals, which are provided in some provinces and districts in Thailand.
| Study group | Role | What they receive |
|---|---|---|
| PLH-Thailand parenting programme | Experimental | Trained facilitators and coaches will deliver the programme over eight weekly sessions at the Udon Thani Regional Hospital during the feasibility pilot and the RCT. During the RCT, the 60 parents/primary caregivers in the intervention group will be divided into 4 groups of 15 participants, with each group overseen by 2 facilitators and 1 coach. Core session activities may include discussion about assigned home activities, core parenting principles, illustrated stories, role-plays, and problem solving. Home visits will be conducted by facilitators to those parents/primary caregivers who miss sessions or require additional support, and SMS/LINE messages will be delivered to all participants twice per week with relevant parenting tips and reminders to attend the upcoming session. Receives: Behavioral: PLH-Thailand parenting programme |
| Control (care as usual) | Other | The control will be an inactive condition of standard care at the time of the intervention. 'Standard care' may include access to Parent Schools in Mother and Child Health clinics at public hospitals, which are provided in some provinces and districts in Thailand. The delivery of services at Parent Schools are guided by the Ministry of Public Health Handbook for Parent Schools, which appear to be open to adaptation at the local level. At Parent Schools, three to five sessions are provided to parents in groups or one-on-one by hospital health personnel. Receives: Other: Control (care as usual) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in frequency of child maltreatment (physical and emotional abuse)
Child maltreatment: physical \& emotional abuse (self-report)
Physical abuse (including abusive discipline) and emotional abuse will be measured using 20 items from an adapted and expanded version of the International Society for the Prevention of Child Abuse and Neglect (ISPCAN) Child Abuse Screening Tool-Trial Caregiver version (ICAST-T). The ICAST-T measures parental reports of the incidence of abuse perpetrated against their child over the past month using a frequency score on a scale of 0 to 7, or 8 or more times (e.g., "In the past 4 weeks, how often did you discipline [Child Nickname] by pushing, grabbing, or kicking him/her?"). This study will assess overall indication of previous child abuse (0 = no abuse; 1 = previous abuse), and frequency of overall abuse by summing all of the subscales. An indication of previous child abuse and a higher frequency of overall abuse represents a worse outcome.
Measured: Differences between groups at T2 (4 months) and T3 (7 months)
Secondary outcomes (17)
Change in frequency of physical and emotional abuse
Child maltreatment: physical and emotional abuse (self-report)
Physical abuse (including abusive discipline) and emotional abuse will be measured using 20 items from an adapted and expanded version of the International Society for the Prevention of Child Abuse and Neglect (ISPCAN) Child Abuse Screening Tool-Trial Caregiver version (ICAST-T). The ICAST-T is an adaptation of the multi-national and consensus-based survey instrument ICAST-Parent version (ICAST-P), which has been used successfully in low and middle-income countries. The ICAST-T measures parental reports of the incidence of abuse perpetrated against their child over the past month using a frequency score on a scale of 0 to 7, or 8 or more times (e.g., "In the past 4 weeks, how often did you discipline [Child Nickname] by pushing, grabbing, or kicking him/her?"). This study will assess incidence of child maltreatment for physical abuse (13 items) and emotional abuse (7 items) by summing each individual subscale.
Measured: Differences between groups at T2 (4 months) and T3 (7 months)
Change in number of instances of physical and emotional abuse
Child maltreatment (physical and emotional abuse) will also be measured through the Home Observation for Measurement of the Environment (HOME) Inventory - Abusive and Harsh sub-scale. The original HOME Early Childhood and Middle Childhood Inventory Forms will be discussed and finalized by the Parenting Experts Working Group during the formative evaluation. The Abusive and Harsh sub-scale is expected to contain six items that utilize dichotomous scoring, with two items assessed via interview in the home regarding whether the parent used physical punishment or yelled at the child during the past week, and four items assessed via observation regarding whether the parent scolded or yelled; used physical restraint; hit, slapped, spanked, or kicked; and pushed, pulled, or pinched the child during the home visit.
Measured: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of child maltreatment (physical and emotional abuse)
Child maltreatment: physical \& emotional abuse (self-report)
Physical abuse (including abusive discipline) and emotional abuse will be measured using 20 items from an adapted and expanded version of the International Society for the Prevention of Child Abuse and Neglect (ISPCAN) Child Abuse Screening Tool-Trial Caregiver version (ICAST-T). The ICAST-T measures parental reports of the incidence of abuse perpetrated against their child over the past month using a frequency score on a scale of 0 to 7, or 8 or more times (e.g., "In the past 4 weeks, how often did you discipline [Child Nickname] by pushing, grabbing, or kicking him/her?"). This study will assess overall indication of previous child abuse (0 = no abuse; 1 = previous abuse), and frequency of overall abuse by summing all of the subscales.
Measured: Differences between groups at T2 (4 months), controlling for T1 (baseline).
Change in frequency of positive parenting
Positive parenting behaviours will be assessed using the Parenting Young Children Scale (PARYC) (21 items), which measures the frequency of positive parenting (7 items), setting limits (7 items) and proactive parenting (7 items) by the parent/primary caregiver over the previous month on a 7-point Likert scale (0 = Never, 6 = Always). Items are summed to create total frequency scores for each subscale.
Measured: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of dysfunctional parenting
Dysfunctional parenting behavior will be assessed using the Arnold Parenting Overreactivity subscale (PS, 10 items), which examines parent attitudes and beliefs regarding authoritarian discipline. PS responses are based on a 7-point Likert scale in which parents are presented with a situation and then are given two opposing responses at either side of the scale, with the mid-point representing neither one way or the other and the three points on either side of the mid-point representing "sometimes," "generally," and "very often" as one moves further out from the middle. One such item under this subscale is "When my child misbehaves, I raise my voice or yell…I speak to my child calmly." (7 = I raise my voice or yell; 1 = I speak to my child calmly.) Scoring for this subscale is computed by averaging the responses on these items.
Measured: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of child monitoring and supervision practices
Parental monitoring and supervision practices will be measured using an adapted version of the Alabama Parenting Questionnaire (APQ) Poor Monitoring/Supervision subscale (11 items). The APQ measures parenting characteristics that have been associated with disruptive behaviour disorders in school-age children, although it has also been used with preschool children. The Poor Monitoring/Supervision subscale will be used to measure the frequency of negative parent monitoring and supervision practices over the past month through a 5-point Likert scale (0 = Never; 5 = Always). Items include "Does (the target child) stay out later than he/she is supposed to?" and "Is (the target child) left at home without adult supervision?" The items in the scale are summed to obtain a total scale score.
Measured: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of child neglect
Child neglect will be assessed using an adapted version of the ICAST-T Caregiver tool (mentioned above) Neglect subscale. This subscale has 6 items for assessing medical, physical, and educational neglect, including "In the past month, how often was [Child Nickname] not taken care of when sick or injured, even when you or another caregiver were able to do so and could afford it?" and "In the past month, how often was [Child Nickname] not given a meal that he or she needed, even when you or another caregiver was able to afford it?"
Measured: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in levels of parental depression, anxiety and stress
Parental depression, anxiety, and stress will be assessed through the Depression, Anxiety, and Stress Scale short form (DASS-21) (21 items) . The DASS-21 will assess parent/primary caregiver depression and anxiety using a 4-point Likert scale [0= Never; 3 = Always] to measure the frequency of symptoms over the previous week. Items include statements such as "I felt that I had nothing to look forward to." Total DASS scores range from 0 to 63, with subscales from 0 to 21. The recommended cut-offs that indicate severity of depression are 5-6 (mild), 7-10 (moderate), 11-13 (severe), and 14 and up (extremely severe), while cut-offs for anxiety are 4-5 (mild), 6-7 (moderate), 8-9 (severe), and 10 and up (extremely severe). Cut-offs for stress are 8-9 (mild), 10-12 (moderate), 13-16 for (severe), and 17 and up (extremely severe).
Measured: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of child behaviour problems
For the purpose of assessing child behaviour problems by parent/primary caregiver self-report, the study will utilize the Eyberg Child Behaviour Inventory (ECBI) Intensity Scale and Problem Scale (36 items). The Intensity Scale measures the frequency of child externalizing behaviours over the past month, using a 7-point Likert-like scale (1 = Never occurs; 7 = Always occurs). Both scales are summed to create a total Intensity Score and Problem Score, with clinical cut-off scores for disruptive behaviour problems suggested as 131 for the Intensity Score and 15 for the Problem Score in the USA. However, no Thai norms are available.
Measured: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in attitudes toward punishment
Attitudes toward punishment will be assessed using one item from the UNICEF Multiple Indicator Cluster Survey (MICS) 5 Child Discipline module. The MICS item asks the parent/primary caregiver: "In order to bring up, raise up, or educate a child properly, the child needs to be physically punished." Parents/primary caregivers will report whether they disagree or agree with the statement based on a 5-point Likert scale of 0 to 4 (0 = Disagree strongly; 4 = Agree strongly).
Measured: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in number of daily child behaviour problems and parenting behaviors
An adapted version of the Parent Daily Report Checklist (PDR, 44 items) will be used to assess day-to-day occurrences of child behaviour problems and parenting behaviour. In order to assess child behaviour, the PDR asks parents/primary caregivers whether a child externalizing behaviour (e.g. destructiveness, lying, hitting others) occurred within the previous 24 hours (34 items), as well as how much sleep the child had (1 item). To assess parenting behaviour, the PDR asks parents about their own behaviour (6 items, e.g. yelled or shouted at the child, praised child for doing something well) and self-efficacy (3 items, e.g. had a feeling that I could not cope with parenting). Responses to these items are dichotomous (0 = No; 1 = Yes), with items summed for each subscale on parent and child behaviour. The item regarding sleep is a numerical response.
Measured: T1: baseline; T2: 1 month; T2: 2 months; T3: 3 months; T4: 6 months
Change in number of positive parent-child interactions
Parent-child relationships will be measured through a combination of interview and observational items (27 in total), using a combined and adapted version of the Early Childhood and Middle Childhood HOME Inventory record forms, as aforementioned. The HOME Inventory is scored dichotomously. The adapted version contains 16 items on the "responsivity" sub-scale; 6 relevant items on the "encouragement of maturity" sub-scale; 2 items on the "emotional climate" sub-scale; and 2 items on the "modelling" sub-scale.
Measured: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of Intimate partner violence
Adult self-report of experiencing intimate partner violence over the past month will be assessed using an adapted version of the Revised Conflict Tactics Scale Short Form (CTS2S, 6 items). This scale includes 2 items on the frequency of negotiation (e.g., "partner suggested a compromise for a disagreement"), 5 items on physical assault (e.g., "partner pushed, shoved, or slapped me"), and 1 item on psychological aggression (e.g., "partner insulted, shouted, yelled, or swore at me"). Answers are coded on a frequency scale of 0 to 3 (0 = never happened; 1 = once or twice; 2 = 3-5 times; 3 = More than 5 times). The CTS2S will determine an overall indication of intimate partner violence on a level of severity (sum of items) and prevalence (dichotomous variable indicating experience of conflict or not), as well as for each subscale.
Measured: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of attitudes towards corporal punishment
Adult report of ICAST-T Attitudes subscale (4 items). These items concern a hypothetical scenario of a child with behavioral problems, and parents report whether different disciplinary methods (e.g., "hitting or spanking the child") were effective or ineffective according to a 5-point Likert scale. Items are summed.
Measured: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of parental sense of inefficacy
Parent sense of inefficacy will be assessed using an adapted version of the ICAST-Trial Inefficacy Subscale (2 items, e.g., "In the past month, how often did you not know what to do when your child misbehaved?") The items are summed for a total score ranging from 0 to 16 with higher scores indicating a greater sense of inefficacy in managing difficult child behaviour.
Measured: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of intimate partner coercion
Adult report of partner coercion based on the WHO questionnaire on women's health and life events (10 items) (Garcia-Moreno, Jansen, Ellsberg, Heise, \& Watts, 2005). The WHO assesses experiences of partner coercion (e.g., "partner took your earnings or savings from you against your will"). Responses are scored on a frequency scale of 0-8, with items for each instrument summed to obtain a total score, as well as a score for the negotiation subscale.
Measured: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of intimate partner negotiation
Adult report of Intimate partner violence (IPV) negotiation (2 items; e.g., "partner suggested a compromise for a disagreement"). Items are summed.
Measured: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted29 May 2018
- Study start11 Dec 2018
- Primary completion31 Jan 2020
- Study completion1 Feb 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Parent Child AbuseStudies of the same condition, open and under way.
- More trials run by University of OxfordThe sponsor's other registered studies.
- 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
- Parallel groups
- Model description
- This study will use a randomised controlled trial design to test the effects of the Parenting for Lifelong Health 2-9 Thailand programme in comparison to participants allocated to receiving care as usual in the control group (N = 120 parents and primary caregivers of children ages 2 to 9 years; 1:1 intervention to control group ratio).
- Masking
- Double blind
- Who is masked
- Investigator, Outcomes assessor
- Enrolment
- 120 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Oxford
- Sponsor type
- University, hospital or other
- Collaborators
- Bureau of Inspection, Ministry of Public Health, Regional Health Center 8 in Udon Thani, Udon Thani Regional Hospital, Boromarajonani College of Nursing (Ministry of Public Health), United Nations Children's Fund (UNICEF) Thailand, Mahidol Oxford Tropical Medicine Research Unit, University of Cape Town
- Responsible party
- Sponsor
- Investigators
- Frances Gardner, DPhil, Principal investigator, University of OxfordJamie Lachman, DPhil, Principal investigator, University of OxfordSombat Tapanya, PhD, Principal investigator, Mahidol Oxford Tropical Medicine Research UnitPhaikyeong Cheah, PhD, Principal investigator, Mahidol Oxford Tropical Medicine Research Unit
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03539341
- Sponsor's protocol ID
- HCR17011
- Status last verified
- May 2022
- First submitted
- 27 Apr 2018
- Last updated
- 12 May 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Following the data analyses, all participant data will be de-identified and stored using United Kingdom Data Archive standards (www.data-archive.ac.uk/create-manage/planning-for-sharing). De-identification will include removal of direct identifiers (names, addresses, postcode information, telephone numbers or pictures) as well as indirect identifiers (information on location, occupation or any other information that could be linked to a public source). This will include removing or aggregating variables or reducing the precision or detailed textual meaning of a variable in the dataset. Access to this data will be controlled and require authorisation from the research team for further use.
Publications
McCoy A, Lachman JM, Ward CL, Tapanya S, Poomchaichote T, Kelly J, Mukaka M, Cheah PY, Gardner F. Feasibility pilot of an adapted parenting program embedded within the Thai public health system. BMC Public Health. 2021 May 29;21(1):1009. doi: 10.1186/s12889-021-11081-4.
PubMed 34051772
Study at a glance
From the registry record, last updated by the sponsor on 12 May 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Randomized Controlled Trial of an Evidence-informed Parenting Intervention to Prevent Violence Against Young Children by Parents and Primary Caregivers in Thailand
- ClinicalTrials.gov ID
- NCT03539341
- Acronym / sponsor ID
- HCR17011
- Conditions
- Parent Child Abuse, Domestic Violence, Child Behavior Problem, Child Neglect, Depression, Anxiety, Parent-Child Relations
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 120 participants (actual)
- Lead sponsor
- University of OxfordUniversity, hospital or other
- Collaborators
- Bureau of Inspection, Ministry of Public Health, Regional Health Center 8 in Udon Thani, Udon Thani Regional Hospital, Boromarajonani College of Nursing (Ministry of Public Health), United Nations Children's Fund (UNICEF) Thailand, Mahidol Oxford Tropical Medicine Research Unit, University of Cape Town
- Study start
- 11 Dec 2018 (actual)
- Primary completion
- 31 Jan 2020 (actual)
- Study completion
- 1 Feb 2020 (actual)
- First posted
- 29 May 2018 (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.
Pilot design:
The feasibility pilot of PLH for Young Children in Thailand has a single-site, pre-post design with no control group, with the aims of assessing programme implementation, cultural and contextual relevance, and study feasibility. Although there is no comparison group and it is not designed to test effects, the pilot also has a provisional goal of reductions in child physical and emotional abuse at one-month post-intervention.
RCT design:
The RCT of PLH for Young Children Thailand is a randomized, controlled, observer-blinded, single-site trial with two parallel groups and a primary endpoint goal of reductions in child physical and emotional abuse at one month and three-months post-intervention. Randomisation will be performed at the individual level with a 1:1 allocation ratio.
Allocation: Using a 1:1 allocation ratio, the 120 participants will be randomly assigned to either the intervention or control group using the concealed computerized programme Sealed Envelope. An external researcher based at the Department of Social Policy and Intervention at the University of Oxford, and who is not directly involved in the study, will generate the random sequence. The Project Coordinator and Co-Investigator McCoy will notify participants of their allocation status via telephone following the collection of baseline data, in order to ensure that participants remain blind to their status during the initial assessment.
Blinding: Due to the involvement of facilitators and coaches in the delivery of the programme, blinding will not be possible for deliverers; moreover, participants cannot be blinded to their allocation status following the initial assessment. However, the allocation status of other participants will be kept concealed from participants in order to reduce the risk of contamination. Data collectors gathering outcome and process evaluation data, as well as statisticians providing support in data analysis, will be blinded to participant allocation status for the purposes of minimizing assessment bias. Cases of compromised blinding will be immediately reported to the Research Manager, who will consult with the research team on an appropriate course of action. Un-blinding of participants will only be permitted if any instances of significant harm due to participation in the study are reported by a participant or any member of the project team at any stage of the study.
This study is funded by the United Nations Children's Fund (UNICEF) Thailand and the Department of Social Policy and Intervention, University of Oxford.
UNICEF grant reference: PCA/THLC/2017/002
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (investigator, outcomes assessor)
- Number of arms
- 2
- Model description
- This study will use a randomised controlled trial design to test the effects of the Parenting for Lifelong Health 2-9 Thailand programme in comparison to participants allocated to receiving care as usual in the control group (N = 120 parents and primary caregivers of children ages 2 to 9 years; 1:1 intervention to control group ratio).
| Arm | Type | Receives |
|---|---|---|
| PLH-Thailand parenting programme | Experimental | Behavioral: PLH-Thailand parenting programmeTrained facilitators and coaches will deliver the programme over eight weekly sessions at the Udon Thani Regional Hospital during the feasibility pilot and the RCT. During the RCT, the 60 parents/primary caregivers in the intervention group will be divided into 4 groups of 15 participants, with each group overseen by 2 facilitators and 1 coach. Core session activities may include discussion about assigned home activities, core parenting principles, illustrated stories, role-plays, and problem solving. Home visits will be conducted by facilitators to those parents/primary caregivers who miss sessions or require additional support, and SMS/LINE messages will be delivered to all participants twice per week with relevant parenting tips and reminders to attend the upcoming session. |
| Control (care as usual) | Other | Other: Control (care as usual)The control will be an inactive condition of standard care at the time of the intervention. 'Standard care' may include access to Parent Schools in Mother and Child Health clinics at public hospitals, which are provided in some provinces and districts in Thailand. The delivery of services at Parent Schools are guided by the Ministry of Public Health Handbook for Parent Schools, which appear to be open to adaptation at the local level. At Parent Schools, three to five sessions are provided to parents in groups or one-on-one by hospital health personnel. |
Who may qualify
- Ages
- 2 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
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 |
|---|---|---|
| PLH-Thailand parenting programmeParenting programmes include developing positive caregiver-child interaction through child-led play and emotional communication, praise and rewards to encourage positive child behaviour, limit-setting behaviours such as effective instruction giving and establishing consistent household rules, and non-violent discipline strategies to replace harsh parenting and corporal punishment. | Behavioural | PLH-Thailand parenting programme |
| Control (care as usual)The control will be an inactive condition of standard care at the time of the intervention. 'Standard care' may include access to Parent Schools in Mother and Child Health clinics at public hospitals, which are provided in some provinces and districts in Thailand. | Other | Control (care as usual) |
Primary outcome
Change in frequency of child maltreatment (physical and emotional abuse)
Time frame: Differences between groups at T2 (4 months) and T3 (7 months)
Child maltreatment: physical \& emotional abuse (self-report) Physical abuse (including abusive discipline) and emotional abuse will be measured using 20 items from an adapted and expanded version of the International Society for the Prevention of Child Abuse and Neglect (ISPCAN) Child Abuse Screening Tool-Trial Caregiver version (ICAST-T). The ICAST-T measures parental reports of the incidence of abuse perpetrated against their child over the past month using a frequency score on a scale of 0 to 7, or 8 or more times (e.g., "In the past 4 weeks, how often did you discipline [Child Nickname] by pushing, grabbing, or kicking him/her?"). This study will assess overall indication of previous child abuse (0 = no abuse; 1 = previous abuse), and frequency of overall abuse by summing all of the subscales. An indication of previous child abuse and a higher frequency of overall abuse represents a worse outcome.
17 secondary outcomes
Change in frequency of physical and emotional abuse
Time frame: Differences between groups at T2 (4 months) and T3 (7 months)
Change in number of instances of physical and emotional abuse
Time frame: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of child maltreatment (physical and emotional abuse)
Time frame: Differences between groups at T2 (4 months), controlling for T1 (baseline).
Change in frequency of positive parenting
Time frame: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of dysfunctional parenting
Time frame: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of child monitoring and supervision practices
Time frame: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of child neglect
Time frame: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in levels of parental depression, anxiety and stress
Time frame: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of child behaviour problems
Time frame: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in attitudes toward punishment
Time frame: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in number of daily child behaviour problems and parenting behaviors
Time frame: T1: baseline; T2: 1 month; T2: 2 months; T3: 3 months; T4: 6 months
Change in number of positive parent-child interactions
Time frame: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of Intimate partner violence
Time frame: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of attitudes towards corporal punishment
Time frame: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of parental sense of inefficacy
Time frame: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of intimate partner coercion
Time frame: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Change in frequency of intimate partner negotiation
Time frame: Differences between groups at T2 (4 months) and T3 (7 months), controlling for T1 (baseline)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 May 2022.
- Results publication: PubMed 34051772McCoy A, Lachman JM, Ward CL, Tapanya S, Poomchaichote T, Kelly J, Mukaka M, Cheah PY, Gardner F. Feasibility pilot of an adapted parenting program embedded within the Thai public health system. BMC Public Health. 2021 May 29;21(1):1009. doi: 10.1186/s12889-021-11081-4.
- Parenting for Lifelong Health - Thailand research project pageLink provided by the sponsor.
- Individual participant dataSharing planned: Yes. Following the data analyses, all participant data will be de-identified and stored using United Kingdom Data Archive standards (www.data-archive.ac.uk/create-manage/planning-for-sharing). De-identification will include removal of direct identifiers (names, addresses, postcode information, telephone numbers or pictures) as well as indirect identifiers (information on location, occupation or any other information that could be linked to a public source). This will include removing or aggregating variables or reducing the precision or detailed textual meaning of a variable in the dataset. Access to this data will be controlled and require authorisation from the research team for further use.
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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.
Frances Gardner, DPhil principal investigator
University of Oxford
Jamie Lachman, DPhil principal investigator
University of Oxford
Sombat Tapanya, PhD principal investigator
Mahidol Oxford Tropical Medicine Research Unit
4 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing PLH-Thailand parenting programme in people with Parent Child Abuse and Domestic Violence, run by University of Oxford at 4 sites in Thailand.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
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: finished, as of the sponsor's last update on 12 May 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 4 sites in Thailand. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Change in frequency of child maltreatment (physical and emotional abuse) (time frame: Differences between groups at T2 (4 months) and T3 (7 months)). 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 NCT03539341, which also lists 1 linked publication.
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 12 May 2022.