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Clinical Trials/NCT01054898
NCT01054898
Completed
Not Applicable

A RCT to Test the Effectiveness of a Telephone Intervention to Improve the Mental Health of Community Dwelling Women Abused by Their Intimate Partners

The University of Hong Kong1 site in 1 country200 target enrollmentFebruary 2007
ConditionsBattered Women

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Battered Women
Sponsor
The University of Hong Kong
Enrollment
200
Locations
1
Primary Endpoint
depression
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to determine if a telephone social support and empowerment intervention is more effective than usual community services in improving the mental health of community-dwelling women abused by their intimate partners.

Detailed Description

Depression is one of the most common mental health sequelae of intimate partner violence (IPV). Although a range of interventions have been tried to improve the mental health of women survivors of IPV, the results are inconclusive. In this trial, a 12-week advocacy intervention consisting of empowerment and telephone social support is provided to abused Chinese women in a community setting. Usual community services provide the control condition.

Registry
clinicaltrials.gov
Start Date
February 2007
End Date
June 2009
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Professor Agnes Tiwari

Professor and Head

The University of Hong Kong

Eligibility Criteria

Inclusion Criteria

  • Chinese women 18 years of age or older
  • Self-report of psychological, physical or sexual abuse by their current or former intimate partner in the previous 12 months
  • Live or work in a community within the catchment area of a community centre designated for the proposed study

Exclusion Criteria

  • Perpetrator is not an intimate partner

Outcomes

Primary Outcomes

depression

Time Frame: On completion of intervention and six months post-intervention

Secondary Outcomes

  • health-related quality of life(On completion of intervention and six months post-intervention)
  • intimate partner violence(On completion of intervention and six months post-intervention)
  • safety behaviors(On completion of intervention and six months post-intervention)
  • perceived social support(On completion of intervention and six months post-intervention)
  • utilization of health services(On completion of intervention and six months post-intervention)

Study Sites (1)

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