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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03813901
Other study ID # NMP/Arsha 2091
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 21, 2018
Est. completion date December 21, 2018

Study information

Verified date January 2019
Source NMP Medical Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Violence has immediate effects on women's health, which in some cases, is fatal. Physical, mental and behavioural health consequences can also persist long after the violence has stopped. Violence against women and girls occurs in every country and culture and is rooted in social and cultural attitudes and norms that privilege men over women and boys over girls.

Research consistently finds that the more severe the abuse, the greater its impact on women's physical and mental health. In addition, the negative health consequences can persist long after abuse has stopped.Present work shares the impact of arsha vidya counselling for women who has been victim of violence.


Recruitment information / eligibility

Status Completed
Enrollment 102
Est. completion date December 21, 2018
Est. primary completion date November 22, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Woman

- Able to attend regular counselling

- Planning to remain in area for next 6 months

- have experience intimate partner violence (physical, emotional, psychological, and/or sexual), including coercive control from a current or former partner in the previous 12 months and no later than 3 years.

Exclusion Criteria:

- Man

- Under 19 years of age

- Cannot attend at regular basis

- Living outside of the selected study sites, or planning to relocate in next 4 months

- Separated more than 3 years ago

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Samalochana Counselling
Counselling program was individual, based on advaita vedanta and traditional philosophical grounds to answer individual fears, concerns,conflicts and difficulties in order to cope and recover.
Wait list control
Wait list had no intervention offered during the study period. Afterwards, they were offered the counselling for the same duration.

Locations

Country Name City State
India Divya Jaipur Rajasthan

Sponsors (3)

Lead Sponsor Collaborator
NMP Medical Research Institute Arsha Vidya Study Centre, Tamilnadu, India, Warwick Research Services

Country where clinical trial is conducted

India, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Quality of Life Quality of Life was measured using SF-36 questionnaire Change from baseline to 12-week
Secondary Change in Anxiety Anxiety was measured using Beck Anxiety Inventory Change from Baseline to 12-weeks
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