Self-questionnaire in Osteoporosis

ConditionOsteoporosis
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCHU de Quebec-Universite Laval

About this trial

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.

Eligibility criteria

Qualifiers

Adult over 18

Followed by the rheumatology or endocrinology clinics at the CHUL (CHU de Quebec-Universite Laval)

Suffer from osteoporosis

Have internet access

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Self-administered questionnaire
  • Family tree

Treatment groups

58 Participants
are divided into 1 treatment group

Sponsors and collaborators