- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06104813
Evaluation of Deaf Men's Knowledge About Sexual Health
Evaluation of Deaf Men's Knowledge About Sexual Health, in Nancy's CHRU
Evaluation of Deaf men's knowledge about sexual health in Nancy, France. The study consists of interviews with voluntary deaf men from Nancy, France, in order to assess their knowledge about sexual health, and determine if there is a lack of sexual health awareness.
If there is indeed a lack of information about sexual health, the study aims at finding ways of improving the situation, and see how the deaf men would like to have this information delivered to them.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Evaluation of Deaf men's knowledge about sexual health in Nancy, France. The study consists of interviews with voluntary deaf men from Nancy, France. The goal is to assess their knowledge about sexual health, and determine if there is a lack of sexual health awareness.
If there is indeed a lack of information about sexual health, the study aims at finding ways of improving the situation, and see how the deaf men would like to have sexual health information delivered to them.
Patients from Nancy's Regional Deaf Healthcare Service (URASSM) will be contacted and volunteers adult deaf men, using sign language as their main langage, will be recruited into the study.
The interviews will consist of a series of open questions aiming to evaluate the volunteers knowledge about sexual health, and evaluate their expectations about how sexual health care for deaf men should be dealt with.
A professional french sign language translator will be present during the interviews, and all the questions and answers will be delivered using french sign language.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Grand Est
-
Nancy, Grand Est, France, 54000
- Central Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Deaf
- Over 18
- Using french sign language
- Whithout curatorship or tutelage
Exclusion Criteria:
- Female
- Under 18
- Non deaf
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
URASSM volunteer deaf men
Volunteer deaf men recruited at Nancy's URASSM Deaf Care Unit (Unité régionale d'accueil et de soins des sourds et malentendants), for individual interviews.
|
Interview with volunteer, to ask them a series of open questions about sexual health in the deaf male population.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Deaf volunteer's sexual health knowledge questionnaire
Time Frame: 1 day Interview
|
Deaf volunteer's sexual health knowledge about sexual violence, STDS, contraceptives
|
1 day Interview
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Deaf volunteer's expectation about sexual health care questionnaire
Time Frame: 1 day Interview
|
Deaf volunteer's expectation about sexual health care, especially how they would like to get information delivered to them, and how a medical consultation dealing with sexual health should be performed.
|
1 day Interview
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2022PI188-398
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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