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临床试验/NCT05566821
NCT05566821已完成不适用

Scaling up Trauma and Violence-Informed Outreach With Women Affected by Violence

University of British Columbia2 个研究点 分布在 1 个国家目标入组 39 人开始时间: 2022年10月5日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
39
试验地点
2
主要终点
Change in trust from baseline to 9 months

研究概览

简要总结

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.

详细描述

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:

  1. How effective is this outreach program in:
  • building trusting relationships with women?
  • supporting women to achieve their self-identified priorities and goals (short-term, medium-term, and long-term goals) in ways that foster safety, autonomy and rights to self-determination?
  1. What factors enable or confound the success of the outreach intervention?

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Self-identify as a woman, therefore the study is trans-inclusive
  • Have some degree of English proficiency in understanding and communication
  • Live and/or spend significant time for work and/or health and social services in the service area of one of the participating community organizations
  • Age 18 or over

排除标准

  • Individuals not meeting the inclusion criteria listed above will be excluded from participation.
  • In addition, women already enrolled in another program with wrap-around supports and who are able to independently navigate health and social care will not be eligible to participate in the outreach program intervention.

结局指标

主要结局

Change in trust from baseline to 9 months

时间窗: 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

Safety in Care Encounters at 12 months

时间窗: 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

Safety in Home Setting at 9 months

时间窗: 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

Safety in Community Setting at 6 months

时间窗: 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

Safety in Community Setting at 12 months

时间窗: 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

Change in trust from baseline to 6 months

时间窗: 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

Change in trust from baseline to 12 months

时间窗: 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

Safety in Care Encounters at 3 months

时间窗: 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

Change in trust from baseline to 3 months

时间窗: 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

Safety in Care Encounters at Baseline

时间窗: 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

Safety in Care Encounters at 6 months

时间窗: 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

Safety in Care Encounters at 9 months

时间窗: 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

Safety in Home Setting at 6 months

时间窗: 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

Safety in Home Setting at 12 months

时间窗: 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

Safety in Community Setting at 9 months

时间窗: 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

Safety in Home Setting at Baseline

时间窗: 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

Safety in Home Setting at 3 months

时间窗: 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

Safety in Community Setting at Baseline

时间窗: 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

Safety in Community Setting at 3 months

时间窗: 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

次要结局

  • Priorities achieved at 3 months(3 months)
  • Priorities achieved at 12 months(12 months)
  • Priorities achieved at 21 months(21 months)
  • Priorities achieved at 24 months(24 months)
  • Priorities achieved at 6 months(6 months)
  • Priorities achieved at 15 months(15 months)
  • Priorities achieved at 18 months(18 months)
  • Priorities achieved at 9 months(9 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Victoria Bungay

Professor

University of British Columbia

研究点 (2)

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