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Survey on the Expectations of Adolescents With Juvenile Idiopathic Arthritis (JIA) Regarding Knowledge and Communication With Health Care Professionals in the Field of Sexual Health, and Their Parents' Views on the Subject. (SNAPS-JIA)

Survey on the Expectations of Adolescents With Juvenile Idiopathic Arthritis (JIA) Regarding Knowledge and Communication With Health Care Professionals in the Field of Sexual Health, and Their Parents' Views on the Subject.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04791189
Acronym
SNAPS-JIA
Enrollment
300
Registered
2021-03-10
Start date
2021-05-31
Completion date
2022-06-30
Last updated
2021-03-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Juvenile Idiopathic Arthritis

Keywords

Juvenile idiopathic arthritis, Sexual health, Patient education, Needs assessment

Brief summary

Sexual health is a legitimate area to explore in the care of these patients, as it has such an impact on quality of life. However, addressing sexual health in a situation of chronic disease confronts the double societal taboo of disease and sexuality. Health professionals are uncomfortable because they are not trained to talk about the subject, especially in the presence of parents and with a teenager they have watched grow up. In this context, a needs survey among juvenile idiopathic arthritis (JIA) patients and the point of view of their parents in the field of sexual health seems necessary. Main objective: To determine the expectations of adolescents (aged 10-19 years) with juvenile idiopathic arthritis regarding knowledge and communication with health care professionals in the field of sexual health.

Detailed description

This study is non-interventional, multi-centre and does not change current practice. It will begin with the construction in a multidisciplinary team of two needs assessment questionnaires, the first for adult patients who have suffered from JIA, the second for their parents. They will be drawn up by three sexologists, two rheumatologists, a pediatrician, a nurse from UTEP, a biostatistician, a statistician specializing in questionnaire metrology, two patients with JIA, two parents of JIA patients, and the Director of the ANDAR patient association. These needs assessment questionnaires, entirely anonymous, will be composed of closed, Likert scale or semi-open questions. The questionnaires will be implemented under RedCap° for patient associations. The material necessary for the study (invitation letter + patients/parents-information letters + paper questionnaires for both surveys + pre-stamped letters) will be in paper format for hospital centres. These centres will ensure the follow-up of the study. The invitation to participate in the survey by mailing or newsletter or association website will be made by the heads of patient associations.

Interventions

OTHERquestionnaire

questionnaire to survey the needs of adolescents with juvenile idiopathic arthritis and the views of their parents in the area of sexual health.

Sponsors

Societe Francaise de Rhumatologie
CollaboratorOTHER
University Hospital, Clermont-Ferrand
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

Patients : * Patients with juvenile rheumatoid arthritis aged from 18 to 45 years * \- Major male or female patient \[18 to 45 years of age\] with juvenile idiopathic arthritis reported before the age of 16. * \- Able to understand and complete the questionnaire online (speaking and reading French, with an internet connection for completion via RedCap°). ¬ * \- Able to give informed consent to participate * \- Involving one's parents in the survey is not a prerequisite for inclusion. Parents : * Parents of patients with juvenile rheumatoid arthritis aged from 18 to 45 years * \- Parents of adult patients with JIA * \- Parents able to understand and complete the questionnaire online (speaking and reading French, having an internet connection for completion via Red Cap°). * \- Able to give informed consent to participate * \- The parents must have been in charge of the patient as a teenager.

Exclusion criteria

* Persons opposing participation in the study. The study information letters will specify that participation is consent to participate in the study. * Protected persons

Design outcomes

Primary

MeasureTime frameDescription
Responses of JIA patients to a questionnaire on their expectations during adolescence regarding knowledge and communication with health professionals in the field of sexual health (patient needs assessment questionnaire) .Day 1Responses of JIA patients to a questionnaire on their expectations during adolescence regarding knowledge and communication with health professionals in the field of sexual health (patient needs assessment questionnaire)

Secondary

MeasureTime frameDescription
Responses of JIA patients to a questionnaire on their expectations during adolescence regarding knowledge and communication with health professionals in the field of sexual health (patient needs assessment questionnaire)Day 1Responses of JIA patients to a questionnaire on their expectations during adolescence regarding knowledge and communication with health professionals in the field of sexual health (patient needs assessment questionnaire) .
Responses of parents of JIA patients to a questionnaire on their child's assumed expectations during adolescence regarding knowledge and communication with health professionals in the field of sexual health (parent needs assessment questionnaire).Day 1Responses of parents of JIA patients to a questionnaire on their child's assumed expectations during adolescence regarding knowledge and communication with health professionals in the field of sexual health (parent needs assessment questionnaire).

Countries

France

Contacts

Primary ContactLise LACLAUTRE
promo_interne_drci@chu-clermontferrand.fr+334 73 754 963

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026