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Behavioural Intervention

Online Parenting Program for Forcibly Displaced Families (PIMonline Trial)

N/A
Recruiting
Led By Abigail Gewirtz, Ph.D.
Research Sponsored by Arizona State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Must not have
Impaired decision-making capacity
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 0-baseline (timepoint 1); 4-month posttest (timepoint 2); 16-month posttest (timepoint 3)
Awards & highlights

Summary

This trial will test an online parenting program called Parenting in the Moment (PIM) for parents who have experienced forced displacement. The study aims to evaluate the effectiveness of the program in improving parenting skills

Who is the study for?
This trial is for families who have been forcibly displaced within the last 10 years and are now in the USA. It's specifically for parents of school-aged children who speak English, Spanish, Arabic, or French. One parent and one child from each family can join. Families already using a similar online parenting program cannot participate.
What is being tested?
The study tests an online parenting program called Parenting in the Moment (PIM) to see if it helps improve skills for parents with forced migration backgrounds. Half of the participating families will use PIM while the other half will receive a resource list only as a control group.
What are the potential side effects?
Since this is not a medical intervention, there are no direct physical side effects expected from participating in this trial. However, participants may experience emotional discomfort when discussing personal experiences or trauma during surveys and tasks.

Eligibility Criteria

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
Select...
I have difficulty making decisions due to my health condition.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~0-baseline (timepoint 1); 4-month posttest (timepoint 2); 16-month posttest (timepoint 3)
This trial's timeline: 3 weeks for screening, Varies for treatment, and 0-baseline (timepoint 1); 4-month posttest (timepoint 2); 16-month posttest (timepoint 3) for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Adult Wellbeing
Caregiver Satisfaction with the intervention
Child Safety
+4 more
Secondary study objectives
Adult Wellbeing

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: Parenting InterventionExperimental Treatment1 Intervention
Participants will receive the PIMonline program and a list of Parenting resources.
Group II: ControlPlacebo Group1 Intervention
Participants will receive a list of Parenting resources. Once the study period ends, they will be given access to the PIMonline program.

Find a Location

Who is running the clinical trial?

Department of Health and Human ServicesFED
230 Previous Clinical Trials
933,909 Total Patients Enrolled
Arizona State UniversityLead Sponsor
294 Previous Clinical Trials
106,710 Total Patients Enrolled
3 Trials studying Mental Health
784 Patients Enrolled for Mental Health
Abigail Gewirtz, Ph.D.Principal InvestigatorArizona State University
1 Previous Clinical Trials
134 Total Patients Enrolled
~480 spots leftby Jun 2026
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