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

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ClinicalTrials.gov Identifier: NCT02437201
Recruitment Status : Unknown
Verified September 2015 by Macmillan Research Group UK.
Recruitment status was:  Active, not recruiting
First Posted : May 7, 2015
Last Update Posted : September 29, 2015
Sponsor:
Collaborators:
Goldington Family Center, UK
Vinita Nursing Home, India
Sonal Foundation, India
Information provided by (Responsible Party):
Macmillan Research Group UK

Brief Summary:
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.

Condition or disease Intervention/treatment Phase
Violence Against Women Behavioral: Liberty Program Not Applicable

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 500 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Prevention
Official Title: Study of Liberty Program on Women's Health and Intimate Partner Violence: Multinational, Open, Randomised, Controlled Clinical Study
Study Start Date : July 2015
Estimated Primary Completion Date : June 2017
Estimated Study Completion Date : December 2017

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Women's Health

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



Primary Outcome Measures :
  1. Quality of Life measured by SF 36 Scale [ Time Frame: Change from baseline in SF 36 Scale at 6 months ]

Secondary Outcome Measures :
  1. Self-Esteem measured by Rosenberg Self-Esteem Questionnaire [ Time Frame: Change from Baseline in Rosenberg Self-Esteem Questionnaire at 6 months ]


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Ages Eligible for Study:   18 Years to 60 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

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.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02437201


Locations
United States, Massachusetts
Liberty USA
Boston, Massachusetts, United States
Australia
Liberty Australia
Melbourne, Australia
China, Shanghai
Liberty China
Shanghai, Shanghai, China
Greece
Liberty Europe
Athens, Greece
India
Sonal Foundation
Mahesana, Gujarat, India
Vinita Nursing Home
Hindaun, Rajasthan, India
Pakistan
Liberty Pakistan
Lahore, Punjaab, Pakistan
South Africa
Liberty Africa
Johannesburg, South Africa
Sponsors and Collaborators
Macmillan Research Group UK
Goldington Family Center, UK
Vinita Nursing Home, India
Sonal Foundation, India
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

Responsible Party: Macmillan Research Group UK
ClinicalTrials.gov Identifier: NCT02437201     History of Changes
Other Study ID Numbers: Mac/NMP 1121
First Posted: May 7, 2015    Key Record Dates
Last Update Posted: September 29, 2015
Last Verified: September 2015