- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02437201
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
Conditions
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
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Melbourne, Australia
- Liberty Australia
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Shanghai
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Shanghai, Shanghai, China
- Liberty China
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Athens, Greece
- Liberty Europe
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Gujarat
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Mahesana, Gujarat, India
- Sonal Foundation
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Rajasthan
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Hindaun, Rajasthan, India
- Vinita Nursing Home
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Punjaab
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Lahore, Punjaab, Pakistan
- Liberty Pakistan
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Johannesburg, South Africa
- Liberty Africa
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Massachusetts
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Boston, Massachusetts, United States
- Liberty USA
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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 |
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No Intervention: Control group
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Experimental: Liberty Group
Weekly intensive support group for women with children who have suffered or are still suffering from domestic abuse (DA).
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
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Quality of Life measured by SF 36 Scale
Time Frame: Change from baseline in SF 36 Scale at 6 months
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Change from baseline in SF 36 Scale at 6 months
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
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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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Change from Baseline in Rosenberg Self-Esteem Questionnaire at 6 months
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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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