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Behavioral Intervention

Positive Parenting Program for Domestic Violence

N/A
Waitlist Available
Led By Doncy J Eapen, PhD, MSN, APRN, FNP-BC
Research Sponsored by The University of Texas Health Science Center, Houston
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Report of at least one physically violent act from a partner within the past 24 months
Have at least one child 5 years or younger
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, immediately after intervention(about 6 weeks after baseline), one month after end of intervention and 3 months after end of intervention intervention
Awards & highlights

Study Summary

"This trial aims to help women who have experienced interpersonal violence and homelessness by improving their skills and self-confidence. They will also be taught positive parenting strategies through a program called Play and Learning Strategies."

Who is the study for?
This trial is for women who have faced domestic violence within the last two years, are currently homeless, and have at least one child under the age of six. Participants must speak English and their violent partner should not be present during enrollment.Check my eligibility
What is being tested?
The study aims to help these women by using a program called Play and Learning Strategies (PALS) to improve parenting skills and cope with trauma from violence and homelessness, compared to usual care they would receive.See study design
What are the potential side effects?
Since this trial involves educational interventions rather than medical treatments, there are no direct physical side effects; however, participants may experience emotional discomfort when discussing personal experiences.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I have experienced physical violence from a partner in the last 2 years.
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I have a child who is 5 years old or younger.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, immediately after intervention(about 6 weeks after baseline), one month after end of intervention and 3 months after end of intervention intervention
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, immediately after intervention(about 6 weeks after baseline), one month after end of intervention and 3 months after end of intervention intervention for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in Women's parenting stress as assessed by the Parental Stress scale (PSS)
Change in children's behavior as assessed by the Devereux Early Childhood Assessments (DECA)-Infant
Change in children's behavior as assessed by the Devereux Early Childhood Assessments (DECA)-Preschoolers
+7 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Positive Parenting ProgramExperimental Treatment1 Intervention
Group II: Usual CareActive Control1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Positive Parenting Program
2011
N/A
~90

Find a Location

Who is running the clinical trial?

The University of Texas Health Science Center, HoustonLead Sponsor
906 Previous Clinical Trials
323,074 Total Patients Enrolled
Rita and Alex Hillman Foundation - Hillman Emergent InnovationUNKNOWN
Doncy J Eapen, PhD, MSN, APRN, FNP-BCPrincipal InvestigatorThe University of Texas Health Science Center, Houston

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is the ongoing medical study actively seeking participants at this time?

"As per the details provided by clinicaltrials.gov, this particular research endeavor is not presently seeking individuals to participate. The trial was first shared on February 19th, 2024 and last revised on January 30th of the same year. While recruitment for this specific study is currently inactive, it's noteworthy that there are nine alternative investigations actively enrolling participants at present."

Answered by AI
~16 spots leftby Jul 2024