Violence Against Women and Consequences During Climacteric´s Phase
NCT ID: NCT01028118
Last Updated: 2010-04-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE3
300 participants
INTERVENTIONAL
2009-04-30
2009-10-31
Brief Summary
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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.
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Therapy for Women reporting violence
Asking about life experience with violence and Cognitive Behavior Therapy.
Identifying experience with violence
Asking about life experience with violence and Cognitive Behavior Therapy.
Interventions
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Identifying experience with violence
Asking about life experience with violence and Cognitive Behavior Therapy.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Women that were not 40 to 65 years.
40 Years
65 Years
FEMALE
Yes
Sponsors
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Conselho Nacional de Desenvolvimento Científico e Tecnológico
OTHER_GOV
Núcleo de Estudos Sobre Violência e Humanização da Assistencia à Saúde
OTHER
University of Sao Paulo General Hospital
OTHER
Responsible Party
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University of Sao Paulo General Hospital
Principal Investigators
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Sandra Dircinha TA Moraes, Post-Doc
Role: PRINCIPAL_INVESTIGATOR
University of Sao Paulo General Hospital
Edmund C Baracat, Titular Prof
Role: STUDY_DIRECTOR
University of Sao Paulo General Hospital
Locations
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Hospital das Clinicas of the Medicine College of the University of São Paulo
São Paulo, São Paulo, Brazil
Countries
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Other Identifiers
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180/09
Identifier Type: -
Identifier Source: org_study_id
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