Self-questionnaire in Osteoporosis
Osteoporosis is a multifactorial disease in which genetic predispositions play a key role in its development. A better understanding of family history and clinical manifestations among first- and second-degree relatives can help improve early detection and personalized care for at-risk patients. To this end, we will te
| Condition(s) | Osteoporosis |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| Summary | Osteoporosis is a multifactorial disease in which genetic predispositions play a key role in its development. A better understanding of family history and clinical manifestations among first- and second-degree relatives can help improve early detection and personalized care for at-risk patients. To this end, we will test a self-administered questionnaire previously developed by our research team. This questionnaire includes the main manifestations associated with rare genetic bone diseases such as osteogenesis imperfecta, hypophosphatasia, and osteopetrosis. |
| Who can participate | Inclusion Criteria: * Adult over 18 * Followed by the rheumatology or endocrinology clinics at the CHUL (CHU de Quebec-Universite Laval) * Suffer from osteoporosis * Have internet access Exclusion Criteria: * Unfit, unable to consent, unable to answer a questionnaire, unknown family history (e.g. adopted person) |
| Ages | 18 Years |
| Sex | All |
| Lead sponsor | CHU de Quebec-Universite Laval |
| Locations | Québec, Quebec, Canada |
| Start date | 2026-04-01 |
| NCT ID | NCT07067827 |
| Official listing | https://clinicaltrials.gov/study/NCT07067827 |