Self-questionnaire in Osteoporosis

Recruiting now

Conditions studied: Osteoporosis

In brief

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.

Key facts

Study ID

NCT07067827

Run by

CHU de Quebec-Universite Laval

People needed

58

Starts

2026-04-01

Expected to finish

2027-12-31

Last updated by the study team

2026-05-08

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify 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 qualify if…

• Unfit, unable to consent, unable to answer a questionnaire, unknown family history (e.g. adopted person)

Where it is running

• CHU de Quebec-Universite Laval — Québec, Quebec, Canada (enrolling)

Full record on ClinicalTrials.gov

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