University of British Columbia
Vancouver, British Columbia, V6T2B5, Canada
NCT Number: NCT05566821
Using a participatory action research design, this study examines the process and impact of implementing an evidence-informed, strengths-based, trauma- and violence-informed outreach program with women at greatest risk of health and social inequities to mitigate the effects of multiple forms of violence in their lives. Through collaboration among community service leaders and staff, women with lived or living experience of gender-based violence, and researchers, this project aims to improve the capacity of organizations to build and sustain effective and trusting relationships with women in order to foster health, well-being, safety, and increased ability to independently navigate their support needs.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Vancouver, British Columbia, V6T2B5, Canada
Using collaborative research activities, an advanced model of the STRENGTH intervention developed in earlier community-based studies is being tested. That evidence showed that women have unique strengths and abilities in navigating their safety, health and well-being, and that a strengths-based approach is critical to communicate respect and build trusting relationships. Trust facilitates women's engagement and retention in health and social care and enhances their capacities to independently navigate these systems. Appropriate, safe, and responsive outreach can effectively improve safety, reduce overdose deaths, and enhance engagement with health and social care.
The study involves a case-based mixed method design to test an empirically driven model for outreach with women affected by violence, through a series of longitudinal studies with diverse sub-groups of women in differing social and geographical contexts. The two-year intervention study is embedded in a larger 7-year national project aimed at building capacity of outreach programs to prevent and mitigate the effects of gender-based violence and advance the theory and practice of community-based, participatory action research.
Intervention-specific Research Questions:
Project Objectives
To generate new knowledge about program delivery to effectively engage with women to:
This research will provide important knowledge about how to more effectively design, implement and evaluate programs and practices that can increase social and health supports and mitigate the effects of gender-based and structural violence. It tests how an empirically driven model of outreach combined with enhanced service integration supports women to identify their priority needs and can bridge the gap in service needs and access with women affected by violence and inequities.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The STRENGTH outreach intervention is a community-led, strengths-based, and trauma- and violence-informed program to support self-identifying women who experience interpersonal and structural gender-based violence. The outreach intervention aims to support individuals to achieve self-identified priorities.
Time frame: Baseline (6 weeks post-enrollment) & 3 months
Change in trust achieved by the program with participants, measured using participants' self-rated trust in program rated from 1 to 5, with higher scores indicating higher trust and comparing baseline to 3 months post-baseline
Time frame: Baseline (6 weeks post-enrollment) & 6 months
Change in trust achieved by the program with participants, measured using participants' self-rated trust in program rated from 1 to 5, with higher scores indicating higher trust and comparing baseline to 6 months post-baseline
Time frame: Baseline (6 weeks post-enrollment) & 9 months
Change in trust achieved by the program with participants, measured using participants' self-rated trust in program rated from 1 to 5, with higher scores indicating higher trust and comparing baseline to 9 months post-baseline
Time frame: Baseline (6 weeks post-enrollment) & 12 months
Change in trust achieved by the program with participants, measured using participants' self-rated trust in program rated from 1 to 5, with higher scores indicating higher trust and comparing baseline to 12 months post-baseline
Time frame: Baseline (6 weeks post-enrollment)
Self-reported safety in clinical care encounters over the past three months using rating of 1 to 5 with higher scores being higher safety
Time frame: 3 months post-baseline
Self-reported safety in clinical care encounters over the past three months using rating of 1 to 5 with higher scores being higher safety
Time frame: 6 months post-baseline
Self-reported safety in clinical care encounters over the past three months using rating of 1 to 5 with higher scores being higher safety
Time frame: 9 months post-baseline
Self-reported safety in clinical care encounters over the past three months using rating of 1 to 5 with higher scores being higher safety
Time frame: 12 months post-baseline
Self-reported safety in clinical care encounters over the past three months using rating of 1 to 5 with higher scores being higher safety
Time frame: Baseline (6-weeks post-enrollment)
Self-reported safety in current home setting for the previous three months using a rating of 1 to 5 with higher scores being higher safety
Time frame: 3 months post-baseline
Self-reported safety in current home setting for the previous three months using a rating of 1 to 5 with higher scores being higher safety
Time frame: 6 months post-baseline
Self-reported safety in current home setting for the previous three months using a rating of 1 to 5 with higher scores being higher safety
Time frame: 9 months post-baseline
Self-reported safety in current home setting for the previous three months using a rating of 1 to 5 with higher scores being higher safety
Time frame: 12 months post-baseline
Self-reported safety in current home setting for the previous three months using a rating of 1 to 5 with higher scores being higher safety
Time frame: Baseline (6-weeks post-enrollment)
Self-reported safety in community for the previous three months using a rating of 1 to 5 with higher scores being higher safety
Time frame: 3 months post-baseline
Self-reported safety in community for the previous three months using a rating of 1 to 5 with higher scores being higher safety
Time frame: 6 months post-baseline
Self-reported safety in community for the previous three months using a rating of 1 to 5 with higher scores being higher safety
Time frame: 9 months post-baseline
Self-reported safety in community for the previous three months using a rating of 1 to 5 with higher scores being higher safety
Time frame: 12 months post-baseline
Self-reported safety in community for the previous three months using a rating of 1 to 5 with higher scores being higher safety
Time frame: 3 months
Were participants' self-identified priorities achieved after 3 months of intervention (yes/no)
Time frame: 6 months
Were participants' self-identified priorities achieved after 6 months of intervention (yes/no)
Time frame: 9 months
Were participants' self-identified priorities achieved after 9 months of intervention (yes/no)
Time frame: 12 months
Were participants' self-identified priorities achieved after 12 months of intervention (yes/no)
Time frame: 15 months
Were participants' self-identified priorities achieved after 15 months of intervention (yes/no)
Time frame: 18 months
Were participants' self-identified priorities achieved after 18 months of intervention (yes/no)
Time frame: 21 months
Were participants' self-identified priorities achieved after 21 months of intervention (yes/no)
Time frame: 24 months
Were participants' self-identified priorities achieved after 24 months of intervention (yes/no)
University of British Columbia
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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