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Wait List Control for Domestic Violence

N/A
Recruiting
Led By Caroline Piotrowski, PhD MPH
Research Sponsored by University of Manitoba
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
mothers self-reported experience of past intimate partner violence, English-speaking, with at least one school-aged child
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up measured 6-8 months post-intervention
Awards & highlights

Study Summary

This trial looks at two programs designed to help Indigenous mothers and children affected by intimate partner violence in Canada.

Who is the study for?
This trial is for Indigenous mothers in Canada who speak English and have experienced intimate partner violence. They must have at least one child of school age to participate.Check my eligibility
What is being tested?
The study is testing two programs: the Mother's Empowerment Program and the Kid's Club Program, both tailored for Indigenous families affected by domestic violence.See study design
What are the potential side effects?
Since these interventions are social support programs rather than medical treatments, they may not have physical side effects but could bring emotional responses or changes.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~measured 6-8 months post-intervention
This trial's timeline: 3 weeks for screening, Varies for treatment, and measured 6-8 months post-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
Child Anxiety
Child Depression
Child trauma symptoms
+3 more
Secondary outcome measures
Child resilience
Maternal resilience
Maternal self esteem
+1 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: Wait List ControlExperimental Treatment1 Intervention
Participants receive intervention after 12 week delay

Find a Location

Who is running the clinical trial?

University of ManitobaLead Sponsor
595 Previous Clinical Trials
199,321 Total Patients Enrolled
Canadian Institutes of Health Research (CIHR)OTHER_GOV
1,345 Previous Clinical Trials
26,453,354 Total Patients Enrolled
Caroline Piotrowski, PhD MPHPrincipal InvestigatorUniversity of Manitoba

Frequently Asked Questions

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

Which individuals are eligible to partake in this experimental study?

"Individuals aged between 6 and 13 years with a history of exposure to domestic violence are eligible for inclusion in this research study. A total of 160 participants will be enrolled in the trial."

Answered by AI

Are individuals still eligible to participate in this ongoing research?

"According to the details on clinicaltrials.gov, this medical trial is actively seeking participants. It was initially posted on February 23rd, 2024 and most recently revised on March 13th, 2024."

Answered by AI

What is the total number of people involved in this clinical trial?

"Affirmative, the details on clinicaltrials.gov reveal that this trial is actively seeking candidates. The study was initially listed on February 23rd, 2024 and last revised on March 13th, 2024. Researchers aim to recruit a total of 160 participants from a single site."

Answered by AI

What is the main objective of this clinical trial?

"This research aims to evaluate the impact of an intervention on child depression over a period of approximately 6-8 months post-treatment. Additional objectives involve assessing child resilience using the Child & Youth Resilience Measure - revised (CYRM-R), measuring maternal social support through the Inventory of Socially Supportive Behaviors, and evaluating maternal self-esteem with the Rosenberg Self-Esteem Scale."

Answered by AI

Is the study open to individuals who are older than 75 years of age?

"Participants aged between 6 and 13 years old are eligible for enrolment in this clinical trial based on the inclusion criteria."

Answered by AI
~107 spots leftby Dec 2025