Could a simple questionnaire unlock hidden genetic clues in osteoporosis?
NCT ID NCT07067827
First seen May 10, 2026 · Last updated May 12, 2026 · Updated 1 time
Summary
This study aims to see if a self-administered questionnaire can accurately capture family history and signs of rare genetic bone diseases in adults with osteoporosis. Researchers will compare the questionnaire results with detailed family trees (pedigrees) from 58 participants. The goal is to improve early detection and personalized care for those at risk.
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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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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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CHU de Quebec-Universite Laval
RECRUITINGQuébec, Quebec, G1V4G2, Canada
Contact Phone: •••-•••-•••• Email: •••••@•••••
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