Could a simple questionnaire uncover hidden genetic bone disorders?

NCT ID NCT07067827

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.

Disclaimer Read more

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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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.

Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • CHU de Quebec-Universite Laval

    RECRUITING

    Québec, Quebec, G1V4G2, Canada

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact