Self-questionnaire in Osteoporosis
Recruiting now NCT07067827
Run by CHU de Quebec-Universite Laval · for 18 and older · All sexes
What this study is about
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 join (things the study team will check)
✅ You may be able to join if…
- Adult over 18
- Followed by the rheumatology or endocrinology clinics at the CHUL (CHU de Quebec-Universite Laval)
- Suffer from osteoporosis
- Have internet access
🚫 You may not be able to join if…
- Unfit, unable to consent, unable to answer a questionnaire, unknown family history (e.g. adopted person)
Where this trial is running
- CHU de Quebec-Universite Laval, Québec, Quebec, Canada
Who to contact
Laetitia Michou, MD PhD · +14185254444 · laetitia.michou@crchudequebec.ulaval.ca
It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT07067827.
Verify everything on the official ClinicalTrials.gov record. Page updated July 2026.