Child AbusePhase 1NCT00153439
Purdue University Parenting Program Attrition
A Phase 1 study testing Motivational enhancements, parent training in people with Child Abuse, run by Centers for Disease Control and Prevention at 1 site in United States.
Trial summary
The purpose of this study is to examine the efficacy of techniques to enhance participation in parenting programs. Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Child Abuse
- What is being tested?
- Motivational enhancements, parent training
- Type of treatment
- Lifestyle or therapy programme
- How many people
- 560 participants
- Where
- 1 siteUnited States
- Study dates
- Jul 2003to Sep 2006
- Phase
- Phase 1
- 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 Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Who may be able to join
- Parents with children 3-5 years old who attend centers in which interventions are offered
Who cannot join
- See above. No other exclusion criteria will be used.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Purdue University Parenting Program Attrition and Compliance Efficacy Trial
The purpose of this study is to examine the efficacy of techniques to enhance participation in parenting programs.
Read the detailed description
This project addresses the problem of involving parents in interventions that promote parenting effectiveness and child coping-competence in preschoolers as a means of reducing risk of child maltreatment (and related adverse developmental outcomes). Purdue University will examine the impact of partnership (organizational involvement in recruitment and retention), cash incentives, and a motivational goal setting component on participation and engagement in the Parenting Our Children to Excellence program, a group intervention for parents and caregivers of preschool children.
- Conditions
- Child Abuse
- Being tested
- Motivational enhancements, parent training
- Keywords
- parenting, motivation, child maltreatment, program attrition
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Motivational enhancements, parent trainingBehavioural
What is being measured
The primary outcome is the main question the study is designed to answer.
Engagement and participation in an 8-week parenting program
Secondary outcomes (1)
Measures of parenting behavior and attitudes, incidents of child maltreatment, measures of child adjustment and functioning
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Sep 2005 (estimated)
- Study startJul 2003
- Study completionSep 2006
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Child AbuseStudies 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 1
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Factorial
- Masking
- Single blind
- Enrolment
- 560 participants
Sponsor and investigators
- Lead sponsor
- Centers for Disease Control and Prevention
- Sponsor type
- US federal agency
- Collaborators
- Purdue University
- Investigators
- Jean E Dumas, Ph.D., Principal investigator, Purdue University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00153439
- Sponsor's protocol ID
- CDC-NCIPC-3928
- Other IDs
- R49/CCR522339-03
- Status last verified
- Sep 2007
- First submitted
- 8 Sep 2005
- Last updated
- 10 Sep 2007
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 10 Sep 2007. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Purdue University Parenting Program Attrition and Compliance Efficacy Trial
- ClinicalTrials.gov ID
- NCT00153439
- Acronym / sponsor ID
- CDC-NCIPC-3928
- Conditions
- Child Abuse
- Keywords
- parenting, motivation, child maltreatment, program attrition
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 560 participants
- Lead sponsor
- Centers for Disease Control and PreventionUS federal agency
- Collaborators
- Purdue University
- Study start
- Jul 2003
- Study completion
- Sep 2006 (actual)
- First posted
- 12 Sep 2005 (estimated)
- 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.
The purpose of this study is to examine the efficacy of techniques to enhance participation in parenting programs.
Detailed description
This project addresses the problem of involving parents in interventions that promote parenting effectiveness and child coping-competence in preschoolers as a means of reducing risk of child maltreatment (and related adverse developmental outcomes). Purdue University will examine the impact of partnership (organizational involvement in recruitment and retention), cash incentives, and a motivational goal setting component on participation and engagement in the Parenting Our Children to Excellence program, a group intervention for parents and caregivers of preschool children.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Factorial
- Masking
- Single blind
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (1 listed)
- Parents with children 3-5 years old who attend centers in which interventions are offered
Key exclusion criteria (1 listed)
- See above. No other exclusion criteria will be used.
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 |
|---|---|---|
| Motivational enhancements, parent training | Behavioural | – |
Primary outcome
Engagement and participation in an 8-week parenting program
1 secondary outcome
Measures of parenting behavior and attitudes, incidents of child maltreatment, measures of child adjustment and functioning
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 10 Sep 2007.
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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.
Jean E Dumas, Ph.D. principal investigator
Purdue University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing Motivational enhancements, parent training in people with Child Abuse, run by Centers for Disease Control and Prevention at 1 site in United States.
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 1 inclusion and 1 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: finished, as of the sponsor's last update on 10 Sep 2007. 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 United States. 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.
What does this phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
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?
Engagement and participation in an 8-week parenting program. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 2007.