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OpenTrials
Completed

NCT Number: NCT01933555

Impact of Women's Empowerment Program for Abused Pregnant Women

Although domestic violence is recognized as major threat in pregnancy, there is no intervention has been developed or test to support women in India. To evaluate the effect of women's empowerment program administered to abused women in order to reduce domestic abuse, improving health status and safety behavior.

Completed

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Key information

Age range

18 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

NMP medical research institute

Jaipur, Rajasthan, 302019, India

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • at least 18 years of age,
  • victims of intimate partner violence, and
  • willing to participate

Exclusion criteria

  • women whose abuser was not their intimate partner or
  • who were unable to consent

Treatment and study plan

Empowerment Program

Behavioral

Primary outcomes

  1. Quality of life(Sf-36)

    Time frame: Five Months

Secondary outcomes

  1. Post natal depression

    Time frame: 5 months

Other outcomes

  1. Domestic Violence Inventory and safety seeking behavior

    Time frame: 5 months

Sponsors and collaborators

Lead sponsor

Macmillan Research Group UK

Industry

Registry information

Official study title

Impact of Women's Empowerment Program for Abused Pregnant Women: A Randomized Controlled Trial

Important dates

Study start
2013
Primary completion
2013
Study completion
2013
First posted
Sep 2, 2013
Registry last updated
Sep 2, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.