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Clinical Trials/NCT07405528
NCT07405528
Not yet recruiting
Not Applicable

Camouflaged WeChat Mini-program-based Intervention for Women Victims of Intimate Partner Violence: Protocol for a Pilot Mixed Methods Study

The University of Hong Kong1 site in 1 country86 target enrollmentStarted: February 1, 2026Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
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

Experimental

The WOMEN Health programme

Intervention: WOMEN Health programme (Behavioral)

Wait-list control group

Active Comparator

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)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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