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Evaluating Violence Against Women Screening in Mexico

Evaluating Violence Against Women Screening in Mexico

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01661504
Enrollment
959
Registered
2012-08-09
Start date
2013-03-31
Completion date
2014-12-31
Last updated
2021-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Domestic Violence

Brief summary

The overall goal of this proposed study is to develop the state of knowledge in the area of gender-based violence and reproductive health by conducting a randomized controlled trial to improve the health care provider's capacity to screen for intimate partner violence and to mitigate associated risk among women health clinic patrons of reproductive age (ages18-44) with recent experiences of physical or sexual partner violence in Mexico City and its surrounding area. The specific research objectives are as follows: 1. To increase mid-level health care providers' capacity to identify Intimate Partner Violence (IPV) and assist women with risk mitigation 2. Utilizing a randomized controlled trial, to assess the impact of an enhanced health care worker screening and counselling program on (a) past year severe IPV (sexual or physical), including severe IPV; (b) reproductive coercion (c) use of community-based resources and safety planning; and (d) quality of life; versus minimum standard of care 3. To qualitatively examine which programmatic components may serve as mechanisms for observed changes stated in the second objective 4. To synthesize study findings and a) create recommendations for clinic-based intervention programs to address IPV in low and middle income countries and b) disseminate information as reports, presentation, and peer-reviewed publications

Interventions

BEHAVIORALIntegrated Screening

The intervention arm will consist of the following components (described in detail below): a) integrated IPV/Sexual and Reproductive Health Screening, b) supportive care, c) safety planning and harm reduction counseling, d) supported referrals, e) booster counseling sessions

Sponsors

Innovations for Poverty Action
CollaboratorOTHER
Mexican National Institute of Public Health
CollaboratorOTHER_GOV
Yale University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 44 Years
Healthy volunteers
Yes

Inclusion criteria

* Ages 18-44 * Currently in heterosexual relationship with a male partner * Responds in affirmative to past year sexual or physical violence

Exclusion criteria

* Cognitive impairment (slurred speech, inability to follow directions) * Seeking treatment for life threatening emergency care * Intends to relocate within 2 years.

Design outcomes

Primary

MeasureTime frameDescription
Change in Intimate Partner Violence Victimization from Baseline12 monthsParticipants will be followed up at 3 months and at 15 months post-baseline to assess intimate partner violence victimization as measured by an adapted Conflict Tactics Scale - 2. This will allow for a 12 month follow-up from the booster counseling session in the intervention group which occurs at 3 months post-baseline.

Secondary

MeasureTime frameDescription
Change in Quality of Life Scorepast month
Change in Use of Community Resources12 monthsAdapted Community Resources Checklist
Change in Safety Planning12 MonthsAdapted Safety Behavior Checklist
Change in Reproductive Coercion12 months

Countries

Mexico

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 20, 2026