Violence Against Women and Consequences During Climacteric´s Phase (DV)

U

University of Sao Paulo General Hospital

Status and phase

Completed
Phase 3

Conditions

Battered Women
Cognitive Behavior Therapy
Violence

Treatments

Other: Identifying experience with violence

Study type

Interventional

Funder types

Other

Identifiers

NCT01028118
180/09

Details and patient eligibility

About

Objective- Analysis of the health status of women who were or are victims of domestic and sexual violence seeking attention at the outpatient clinic for Endocrines Gynecology and Climactery - University of Sao Paulo General Hospital. To widen the comprehension of the binomial relationship violence-pathologies by professionals/staff who work in health services, offering women in such situation humane, comprehensive and qualified attention. Specific Objectives: decreasing the rates of domestic and sexual violence against women employing: prevention, health education and treatment - within the context of health services and public policies. Methodology - Project Type: Research in Action A- Attention to women in a situation of domestic and sexual violence during climactery; B- Information/Education/Communication (IEC) C- Behavioral Intervention (IC) D- Institutional Development (DI). Target Populations: 1. Women (during the ages of 40 to 65 years) who were or are victims of domestic and/or sexual violence; 2. Professional/staff who work in services attending women in sexual and domestic violent situations (health professionals, policemen, civil society) in areas located within the South Regional Health Coordination - SRC. To collect information, a semi structured questionnaire will be employed during seven months in 2009.

Full description

Trained professionals will work in the regions of: Campo Limpo, M'Boi Mirim, Santo Amaro and neighboring regions, neighborhood in which the Social Vulnerability Index of São Paulo (IPVS) shows high records.

Enrollment

300 patients

Sex

Female

Ages

40 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Women (during the ages of 40 to 65 years) who were or are victims of domestic and/or sexual violence

Exclusion criteria

  • Women who were not victims of domestic and/or sexual violence.
  • Women that were not 40 to 65 years.

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

300 participants in 1 patient group

Therapy for Women reporting violence
Other group
Description:
Asking about life experience with violence and Cognitive Behavior Therapy.
Treatment:
Other: Identifying experience with violence

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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