Recruiting

Observational Study

Sponsor:

CHU de Quebec-Universite Laval

Code:

NCT07067827

Conditions

Osteoporosis

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Self-administered questionnaire

Family tree

Study Details

Brief summary:

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.

Conditions

Osteoporosis

Study ID

NCT07067827

Start date

Apr 1, 2026

Status verified date

May, 2026

Completion date

Dec 31, 2027

Anticipated

Primary completion date

Jul 31, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Adult over 18
  • Followed by the rheumatology or endocrinology clinics at the CHUL (CHU de Quebec-Universite Laval)
  • Suffer from osteoporosis
  • Have internet access

Exclusion Criteria:

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

Study Design

Enrollment

58 participants

Anticipated

Interventions and Outcome Measures

Arms

Group starting with the self-administered questionnaire followed by the family tree and vice versa

Recruited patients will be randomized to either start with the self-administered questionnaire or the family tree. Then, 3 months later, those who started with the questionnaire will be able to do the interview for the family tree and vice versa.

Interventions

Self-administered questionnaire

The self-administered questionnaire was previously prepared by the research team for another project. It includes 14 questions addressing the dentition, fractures, joint hypermobility, height, and eye abnormalities present in the participants or their relatives. This questionnaire covers the clinical manifestations of rare bone diseases such as osteogenesis imperfecta, pycnodysostosis, hypophosphatasia, and osteopetrosis. This self-administered questionnaire will be filled online by participant. Average completion time of 20 minutes.

Family tree

For the family tree, this step is done by a telephone interview lasting a maximum of 45 minutes, depending on the size of the participant's family. The researcher will be able to reconstruct the family history with the index case. The family tree will then contain the family history up to the second degree of kinship with respect to the index cases. The information collected through the index cases when creating the family tree must include, for each relative, biological sex, as well as information on the presence or absence of a rare or genetic bone disease and clinical signs associated with these diseases, such as short stature, bone deformities, deafness, eye problems, etc.

Primary outcome measure

  • Concordance between the results of the self-questionnaire compared to those obtained by a family tree. [ Time Frame: 3 months ]

Central Contacts and Locations

Central contacts

Locations

CHU de Quebec-Universite Laval

Recruiting

Québec, Quebec, Canada, G1V4G2

Contacts

Principal Investigator:

Laetitia Michou, MD PhD

More Information

Sponsor

CHU de Quebec-Universite Laval

Last update posted

May 8, 2026

Last verified

May, 2026

Keywords

  • osteoporosis
  • self-administered questionnaire
  • family history
  • rare genetic bone diseases

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by CHU de Quebec-Universite Laval on 2026-05-08.