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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05206123
Other study ID # APHP211568
Secondary ID 2021-A02820-41
Status Completed
Phase
First received
Last updated
Start date March 17, 2022
Est. completion date September 7, 2022

Study information

Verified date July 2023
Source Assistance Publique - Hôpitaux de Paris
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To improve the knowdelge about the sexual health needs of perinatally HIV-infected adolescents living in France.


Description:

20 individual semi-structured interviews will be conducted with 20 young adults living with HIV sinc childhood and living in France. The aim of this study is to identify their sexual needs through exploring their personal experience of sexuality during their adolescence. The investigator intend to explore communication about the disease and sexuality within their families ; communication about sexual health with health care professionnals ; whether sexuality has arrose difficulties related to their chronic condition such as rejection or sadness ; whether there are differences in sexual needs regarding gender. A thematic analysis will be conducted by three researchers.


Recruitment information / eligibility

Status Completed
Enrollment 27
Est. completion date September 7, 2022
Est. primary completion date September 7, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 25 Years
Eligibility Inclusion Criteria: - Age between 18 and 25 yo - HIV-1 or HIV-2 diagnosis before the age of 13 - non opposition to participate to the study - be affiliated to a social security scheme (except Aide Médicale de l'Etat (AME)) Exclusion Criteria: - having contracted HIV infection through sexual contact - persons under guardianship or custodianship, or deprived of their liberty by a judicial or administrative decision - associated illnesses or disabilities that makes participation impossible

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Interview
Patients will be interviewed with a semi-structured qualitative interview in order to know how they lived their first sexual experiences and their sex lives during their adolescence

Locations

Country Name City State
France Maison de Solenn Paris

Sponsors (2)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris INSERM CESP1018

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Qualitative analysis emerging themes describing the experience of their sexual health needs from the content analysis of the transcribed interviews through study completion, an average of 1 year
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