Community-based intervention for women exposed to intimate partner violence: A randomized control trial.
Sandra A Graham-Bermann, Laura Miller-Graff
https://pubmed.ncbi.nlm.nih.gov/26030027Actively Recruiting
Led by University of Manitoba ยท Updated on 2024-03-15
160
Participants Needed
1
Research Sites
30 weeks
Total Duration
U
University of Manitoba
Lead Sponsor
C
Canadian Institutes of Health Research (CIHR)
Collaborating Sponsor
Researchers are evaluating two evidence-based programs, the Mother's Empowerment Program and Kid's Club Program, specifically adapted for Indigenous mothers and children who have experienced intimate partner violence (IPV) in Canada. The purpose is to test the feasibility of these adapted interventions using both Western and Indigenous knowledge and methods. The study aims to assess changes in mental and physical health, including symptoms of depression, anxiety, and trauma, as well as resilience and well-being over time. The interventions involve weekly group sessions for mothers and children, conducted separately but simultaneously over 10 weeks. Participants receive the intervention after a 12-week waiting period. The study adapts these programs through a collaborative process involving Indigenous community partners and Elders to ensure cultural relevance and appropriateness. During the study, mothers and children will complete standardized questionnaires and participate in interviews and narratives to measure mental health symptoms and resilience immediately after the intervention and again 6 to 8 months later. The research team will monitor changes in depression, anxiety, traumatic stress, social support, and self-esteem. Participant engagement and feedback are integral to the evaluation process throughout the study duration.
CONDITIONS
Healing Circles: An Intervention for Canadian Indigenous Mothers & Children Affected by IPV
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You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 10 weeks
Participants attend weekly group sessions for mothers and children separately, focusing on empowerment and support over 10 weeks.
Weekly visits for 10 weeks
Duration - 6 to 8 months
Participants are followed up to assess sustained changes in mental and physical well-being 6 to 8 months after the intervention ends.
1 to 2 visits depending on assessments
Total: 1 location
1
Discovery House
Calgary, Alberta, Canada, T2A 7R7
Actively Recruiting
C
Caroline Piotrowski, PhD MPH
N
Nicole Letourneau, PhD RN
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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Sandra A Graham-Bermann, Laura Miller-Graff
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