- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00185016
Women Abuse and the Role of the Family Doctor.
Women Abuse and the Role of the Family Doctor. Testing an Intervention in a Randomised Controlled Trial.
The study tested a training to improve recognition of abused female patients in family practice.Effect measures of the training were: number of reported cases wherein the doctor suspected and discussed partner abuse and the number of non-obviuos reasons to suspect partner abuse.We assumed that following a training would improve the recognition of abused women.
Secondary to this trial we explored gender differences of family doctors in discussing partner abuse and we interviewed women recently identified by their family doctor. Medical histories of recently identified abused women were studied to assess health problems and health-care utilisation.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Nijmegen, Netherlands, 6500 HB
- Radboud University Medical Centre
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:women consulting in family practice, age 18 years and older -
Exclusion Criteria:we excluded only for the interviews: women who were assessed by their family doctor to be in danger because of the abusive situation, women with a psychiatric condition.
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Study Plan
How is the study designed?
Design Details
- Primary Purpose: Educational/Counseling/Training
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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number of reported cases wherein a doctor suspected and discussed partner abuse.
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Secondary Outcome Measures
Outcome Measure |
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number of cases with non-obvious symptoms wherein a doctor suspected partner abuse.
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Collaborators and Investigators
Collaborators
Investigators
- Study Chair: Toine LM Lagro-Janssen, PhD/MD/FP, Radboud University Medical Centre Nijmegen
- Principal Investigator: Sylvie H Lo Fo Wong, MD/FP, Radboud University Medical Centre, Nijmegen
Study record dates
Study Major Dates
Study Start
Study Completion
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 1,SLFW
- Theia 200173
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