Could a simple questionnaire uncover hidden genetic bone disorders?

NCT ID NCT07067827

Recruiting now Knowledge-focused Sponsor: CHU de Quebec-Universite Laval Source: ClinicalTrials.gov ↗

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

Researchers are testing a 14-question survey to see if it can help detect rare genetic bone diseases (like osteogenesis imperfecta) in adults with osteoporosis. The study will enroll 58 participants who will fill out the online questionnaire. The goal is to see if the questionnaire matches information from a detailed family tree, which could improve early detection and personalized care.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance: Self-administered questionnaire
What this could lead to: If successful, this questionnaire could help doctors identify patients with rare genetic bone diseases earlier, leading to more personalized care.
What could go wrong: This is a small, early-stage validation study (58 participants) testing a questionnaire, not a treatment. It may not prove accurate enough for widespread use.

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Conditions

The condition(s) this trial relates to.

osteoporosis

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

OSTEOPOROSIS

Contacts and locations

Locations

CHU de Quebec-Universite Laval
RECRUITING

Québec, Quebec, G1V4G2, Canada

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