Perception of Hormonal Replacement Therapy Among Patients Aged 11 to 17 Years
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Female Hypogonadism. Basic parameters: 11 years — 18 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Current Knowledge and Perceptions of Hormone Replacement Therapy Among Patients Aged 11 to 18 Years, and Their Parents, Treated for Hypogonadism at the Strasbourg University Hospital
Overview
To establish a current knowledge and perception of patients and their parents regarding HRT in order to assess the needs that can promote understanding and adherence to treatment by implementing therapeutic education workshops
Primary outcome measures
- Assessment of patients' knowledge about the composition of hormonal treatment for female hypogonadism [Time frame: Up to 7 months]
- Assessment of patients' knowledge regarding the effects of hormonal treatment for female hypogonadism [Time frame: Up to 7 months]
Eligibility criteria
Inclusion criteria
- Female patients aged 11 to 18 years
- Treated at the University Hospital of Strasbourg for central or peripheral hypogonadism with the initiation of hormone replacement therapy
Exclusion criteria
\- Inability to provide the subject with clear information (difficulties understanding the subject, language barrier, illiteracy, etc.)
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Study design
- Observational model
- Case-only
Study locations
France · 1 center
- Service de Gynécologie et obstétrique - CHU de Strasbourg - France — Strasbourg
Identifiers
NCT: NCT07315932 · 9620