Study of Liberty Program on Women's Health and Intimate Partner Violence

September 27, 2015 updated by: Macmillan Research Group UK

Study of Liberty Program on Women's Health and Intimate Partner Violence: Multinational, Open, Randomised, Controlled Clinical Study

Previous studies indicated high frequency of abuse in families and its consequences. Considering the importance of interventions such as educational interventions, in order to increase women's abilities to prevent abusive behaviors, the current research aims to determine the impact of an Liberty program on prevention of violence against women and propose solutions for less damages and consequences.

Study Overview

Status

Unknown

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

500

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Melbourne, Australia
        • Liberty Australia
    • Shanghai
      • Shanghai, Shanghai, China
        • Liberty China
      • Athens, Greece
        • Liberty Europe
    • Gujarat
      • Mahesana, Gujarat, India
        • Sonal Foundation
    • Rajasthan
      • Hindaun, Rajasthan, India
        • Vinita Nursing Home
    • Punjaab
      • Lahore, Punjaab, Pakistan
        • Liberty Pakistan
      • Johannesburg, South Africa
        • Liberty Africa
    • Massachusetts
      • Boston, Massachusetts, United States
        • Liberty USA

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 60 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Be married,
  • Be under the aegis of Foundation at least for a year,
  • Have at least one child.

Exclusion Criteria:

  • Not participating in two educational sessions,
  • Not being interested in continuing the cooperation.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control group
Experimental: Liberty Group
Weekly intensive support group for women with children who have suffered or are still suffering from domestic abuse (DA).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Quality of Life measured by SF 36 Scale
Time Frame: Change from baseline in SF 36 Scale at 6 months
Change from baseline in SF 36 Scale at 6 months

Secondary Outcome Measures

Outcome Measure
Time Frame
Self-Esteem measured by Rosenberg Self-Esteem Questionnaire
Time Frame: Change from Baseline in Rosenberg Self-Esteem Questionnaire at 6 months
Change from Baseline in Rosenberg Self-Esteem Questionnaire at 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Bharat B Chaudhari, MA, Sonal Foundation, India
  • Study Director: Paramjeet S Makkar, MD, Vinita Nursing Home, India
  • Study Chair: Michael Howe, MA, Goldington Family Centre, UK
  • Study Director: Avinash Mishra, MA, Shanghai University, China

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2015

Primary Completion (Anticipated)

June 1, 2017

Study Completion (Anticipated)

December 1, 2017

Study Registration Dates

First Submitted

May 3, 2015

First Submitted That Met QC Criteria

May 6, 2015

First Posted (Estimate)

May 7, 2015

Study Record Updates

Last Update Posted (Estimate)

September 29, 2015

Last Update Submitted That Met QC Criteria

September 27, 2015

Last Verified

September 1, 2015

More Information

Terms related to this study

Other Study ID Numbers

  • Mac/NMP 1121

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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