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Clinical Trials/NCT01958554
NCT01958554
Completed
Phase 2

Randomised Controlled Trial of an Integrated Intervention on Mental Health in Survivors of Intimate Partner Violence

Macmillan Research Group UK1 site in 1 country120 target enrollmentOctober 2013
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ConditionsDomestic Violence

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Domestic Violence
Sponsor
Macmillan Research Group UK
Enrollment
120
Locations
1
Primary Endpoint
Depression
Status
Completed
Last Updated
10 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

Intimate partner violence (IPV) against women have negative mental health consequences for survivors; interventions designed to improve survivors' depressive symptoms and health status are limited.Present study evaluate the effectiveness of an integrated intervention in reducing intimate partner violence (IPV) improving health status.

Registry
clinicaltrials.gov
Start Date
October 2013
End Date
June 2014
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Macmillan Research Group UK
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • •Women over 18
  • •For those who agreed to participate
  • •Given written consent
  • •Screening for abuse was positive

Exclusion Criteria

  • •Screened Negative
  • •serious mental condition including suicide, hallucination, Dementia
  • •Drug or substance abuse, alcoholism

Outcomes

Primary Outcomes

Depression

Time Frame: Change from Baseline in Beck Depression Inventory at 12 weeks

Secondary Outcomes

  • Health Related Quality of Life(Change from baseline in SF-36 at 12 weeks)

Study Sites (1)

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