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

Overview

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.

Full Title of Study: “Study of Liberty Program on Women’s Health and Intimate Partner Violence: Multinational, Open, Randomised, Controlled Clinical Study”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Prevention
    • Masking: Single (Outcomes Assessor)
  • Study Primary Completion Date: June 2017

Interventions

  • Behavioral: Liberty Program

Arms, Groups and Cohorts

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

Clinical Trial Outcome Measures

Primary Measures

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

Secondary Measures

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

Participating in This Clinical Trial

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.

Gender Eligibility: Female

Minimum Age: 18 Years

Maximum Age: 60 Years

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • Macmillan Research Group UK
  • Collaborator
    • Goldington Family Center, UK
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Bharat B Chaudhari, MA, Study Director, Sonal Foundation, India
    • Paramjeet S Makkar, MD, Study Director, Vinita Nursing Home, India
    • Michael Howe, MA, Study Chair, Goldington Family Centre, UK
    • Avinash Mishra, MA, Study Director, Shanghai University, China

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