Camouflaged WeChat Mini-program-based Intervention for Women Victims of Intimate Partner Violence: Protocol for a Pilot Mixed Methods Study
Overview
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- The University of Hong Kong
- Enrollment
- 86
- Locations
- 1
- Primary Endpoint
- Feasibility and acceptability of the WOMEN Health programme
Overview
Brief Summary
Intimate partner violence (IPV) is a major public health issue and human rights threat worldwide, especially for Chinese immigrant women victims in Hong Kong. Interventions that address negative physical and emotional outcomes from IPV could therefore play a crucial role in enhancing empowerment, social support, and healthy lifestyle among these women. The overall objective of this pilot mixed methods study is to determine the feasibility and acceptability of a camouflaged WeChat mini-program-based WOMEN Health intervention for women victims of IPV. This study will evaluate the feasibility and acceptability of a camouflaged WeChat mini-program-based WOMEN Health intervention for women victims of IPV.
Detailed Description
Intimate partner violence (IPV) is a major public health issue and human rights threat worldwide, especially for Chinese immigrant women victims in Hong Kong. Interventions that address negative physical and emotional outcomes from IPV could therefore play a crucial role in enhancing empowerment, social support, and healthy lifestyle among these women. Previous studies in Hong Kong and the United States provided evidence on IPV interventions among Chinese abused women; however, there is a scarcity of evidence on the use of mHealth for abused women while fully considering their safety studies on mobile technology for Chinese immigrant women victims are limited, and there lacks safe, low-cost, and evidence-based mHealth interventions for empowering and supporting women victims who immigrate to Hong Kong and face more vulnerabilities and needs. This study will evaluate the feasibility and acceptability of a camouflaged WeChat mini-program-based WOMEN Health intervention for women victims of IPV.
This pilot mixed methods study will adopt the randomized, wait-list controlled trial with two groups (1:1 ratio), followed by in-depth interviews with participants in the WOMEN Health programme group at post-intervention. It will evaluate feasibility and acceptability as the primary outcomes and compare scores changes after 12 weeks interventions between Chinese immigrant women who are screened positive for IPV randomly assigned to receiving genuine IPV intervention and disguised healthy lifestyle intervention, and Chinese immigrant women who are screened positive for IPV in a control procedure. The wait-list control group will also receive the WOMEN Health programme after the intervention group completed the programme.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Supportive Care
- Masking
- Single (Outcomes Assessor)
Eligibility Criteria
- Ages
- 18 Years to 45 Years (Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Chinese-speaking (Mandarin or Cantonese)
- •women aged 18 to 45 years
- •originally from mainland China and have moved to Hong Kong for at least one year
- •screened positive for IPV during heterosexual relationships in the past year
- •have a smartphone with WeChat installed
- •with no plans to move outside Hong Kong in the next one year
Exclusion Criteria
- •unwilling to provide informed consent
- •severe chronic diseases (e.g., cancer, heart failure, kidney failure, chronic obstructive pulmonary disease, and HIV/AIDS)
- •currently experience severe IPV (identified using the revised 11-item Danger Assessment)
Arms & Interventions
WOMEN Health group
The WOMEN Health programme
Intervention: WOMEN Health programme (Behavioral)
Wait-list control group
Healthy lifestyle intervention
Intervention: Wait-list control group (Behavioral)
Outcomes
Primary Outcomes
Feasibility and acceptability of the WOMEN Health programme
Time Frame: Week 12
Feasibility and acceptability will be assessed using a 12-item self-developed questionnaire. Items are rated on a 5-point Likert scale (1-5), with higher scores indicating greater acceptability, satisfaction, and usefulness.
Secondary Outcomes
- Changes in depressive symptoms(Baseline and Week 12)
- Changes in quality of life(Baseline and Week 12)
- Changes in intimate partner violence (IPV)(Baseline and Week 12)
- Changes in Body Mass Index (BMI)(Baseline and up to 12 weeks)
- Changes in healthy behaviors(Baseline and Week 12)