Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
155 participants
INTERVENTIONAL
2011-07-31
2012-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Aim 1. Triple P's Effect on Pediatric Resident's Practice: test the effect of Triple P training on practice of pediatric residents in addressing and managing psychosocial problems.
Hypothesis 1: At the completion of the trial, residents assigned to the intervention group, compared to residents exposed to the control condition, will have:
1. increased skill levels,
2. increased confidence, and
3. increased satisfaction in dealing with and managing psychosocial issues
Aim 2. Triple P's Effect on Parent and Child Outcomes: test the effect of Triple P interventions on parent's feelings of self efficacy, parent's discipline strategies and on children's externalizing behavior.
Hypothesis 2: At the completion of the intervention, parents and children receiving the intervention, compared to those receiving the control condition, will have:
1. greater reduction in targeted child behavior problems,
2. greater reduction in dysfunctional parenting practices,
3. increased use of appropriate discipline and positive parenting strategies, and
4. greater confidence in parenting ability.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Evaluating an Online Parenting Support System Disseminated by Pediatric Practices
NCT02064452
Evaluation of a Parenting and Stress Management Programmme
NCT01777724
Sleep Health in Preschoolers: a Randomized Controlled Trial
NCT02255721
Primary Care Stepping Stones Triple P for Children With Autism
NCT02236650
Investigating a Brief Virtual Seminar Series for Parents of Children Ages 2-12
NCT06865183
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
SINGLE_GROUP
HEALTH_SERVICES_RESEARCH
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Trained in Primary Care (PC) Triple P
This group received standardized training in Primary Care (PC) Triple P.
Training in PC Triple P
PC Triple P is a brief parenting intervention combining specific advice from provider with parent rehearsal and self-evaluation.
Care as Usal
This group provided care as usual. This group was not trained in PC Triple P interventions.
Care As Usual
Pediatric residents not exposed to PC Triple P provide their standard care to parents struggling with parenting issues or child behavior concerns.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Training in PC Triple P
PC Triple P is a brief parenting intervention combining specific advice from provider with parent rehearsal and self-evaluation.
Care As Usual
Pediatric residents not exposed to PC Triple P provide their standard care to parents struggling with parenting issues or child behavior concerns.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Parent of an eligible child.
* Speaks English
* Treated by a participating resident
* Between 18 months and 12 years old
* Does not have any mental health diagnosis
* Is not receiving medication or therapy from a professional
Exclusion Criteria
* A parent of an ineligible child
* Non-English speaking
* Not treated by a participating resident
* Age falls outside of eligible range
* Has a mental health diagnosis
* Currently receiving medication or therapy from a professional
18 Months
12 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Doris Duke Charitable Foundation
OTHER
Seattle Children's Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Fred Rivara
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Frederick P Rivara, MD, MPH
Role: PRINCIPAL_INVESTIGATOR
Seattle Children's Research Institute, Seattle Children's Hospital, University of Washington
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
SCH-13683
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.