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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03469739
Other study ID # UoB2646
Secondary ID
Status Completed
Phase
First received June 10, 2016
Last updated March 16, 2018
Start date June 2016
Est. completion date August 2017

Study information

Verified date January 2018
Source University of Bristol
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study uses data from 29,990 women from 12 different countries collected by the WHO multi-country study on women's health and domestic violence to capture the effect of different types, frequency and timing of IPV on self-reported health, symptoms and suicidal behaviours.


Description:

Intimate partner violence (IPV) has detrimental effects on physical and mental health, risks to children and is associated with wider societal and healthcare costs. Previous analysis of the WHO multi-country study on women's health and domestic violence found significant associations between physical and sexual IPV and self-reported ill-health, symptomatology and suicidal behaviours.

Real experience of IPV can comprise different combinations of emotional, physical and sexual abuse, and different timings and frequencies of these. A more nuanced testing of exposure to these different combinations of IPV and associations with health is needed.

This study uses data from 29,990 women from 12 different countries collected by the WHO multi-country study on women's health and domestic violence to capture the effect of different combination types, frequency and timing of IPV on self-reported health, symptoms and suicidal behaviours.


Recruitment information / eligibility

Status Completed
Enrollment 29990
Est. completion date August 2017
Est. primary completion date August 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 15 Years to 49 Years
Eligibility Inclusion Criteria:

- The WHO report that in most sites, a representative sample of women was obtained using a two-stage cluster sampling scheme to select households and then only one woman per household was randomly selected per household for interview.

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Bristol

References & Publications (2)

Ellsberg M, Jansen HA, Heise L, Watts CH, Garcia-Moreno C; WHO Multi-country Study on Women's Health and Domestic Violence against Women Study Team. Intimate partner violence and women's physical and mental health in the WHO multi-country study on women's health and domestic violence: an observational study. Lancet. 2008 Apr 5;371(9619):1165-72. doi: 10.1016/S0140-6736(08)60522-X. — View Citation

Garcia-Moreno C, Jansen HA, Ellsberg M, Heise L, Watts CH; WHO Multi-country Study on Women's Health and Domestic Violence against Women Study Team. Prevalence of intimate partner violence: findings from the WHO multi-country study on women's health and domestic violence. Lancet. 2006 Oct 7;368(9543):1260-9. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Participant description of their current overall state of health Participant description of their current overall state of health- a choice of options- excellent, good, fair, poor or very poor. Preceding 4 weeks
Secondary Participant reported health in the last 4 weeks- problems walking around, doing usual activities, pain or discomfort, problems with memory or concentration, dizziness or vaginal discharge. Measured by questionnaire. Participant rating of various health aspects in last 4 weeks Preceding 4 weeks
Secondary Emotional distress. Measured by questionnaire of 20 different symptoms of emotional distress. SRQ-20 (score of 20 different symptoms of emotional distress with yes/no answers) Self Reporting Questionnaire-20 (SRQ-20)- aggregate score of 20 different symptoms of emotional distress with yes/no answers Preceding 4 weeks
Secondary Participant reported ever suicidal thoughts or attempts; measured by questionnaire. Participants reporting ever having suicidal thoughts or ever attempting suicide Up to 49 years
Secondary Participant reported medication used for sleep/ pain; measured by questionnaire. Participants reporting medication use Preceding 4 weeks
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