Status:
UNKNOWN
Recognizing Osteoporosis and Its Consequences in Quebec (ROCQ) Programme
Lead Sponsor:
CHU de Quebec-Universite Laval
Collaborating Sponsors:
Merck Frosst Canada Ltd.
Sanofi
Conditions:
Osteoporosis
Eligibility:
FEMALE
50+ years
Phase:
NA
Brief Summary
The aim of the ROCQ programme is to improve the use of evidence based osteoporosis diagnostic and treatment strategies for women 50 years and over who have suffered a fragility fracture. This objectiv...
Detailed Description
ROCQ is a patient health-management programme and prospective cohort study. Within the ROCQ programme, educational interventions to improve osteoporosis management will be evaluated using a randomized...
Eligibility Criteria
Inclusion
- Female, aged 50 years and over.
- Not residing in a long-term care hospital before the fracture.
- Able to understand the programme information and consent form.
- Must voluntarily accept to participate in this programme and sign the consent form.
- Participants must have a fragility or traumatic fracture of one of the following sites: wrist, forearm, humerus, scapula, clavicle, sternum, thoracic or lumbar vertebrae, pelvis, sacrum, hip, femur, proximal and distal tibia, fibula (including ankle), and foot.
- Participants must be able to answer the questionnaires via phone interviews
Exclusion
- Unable to understand the purpose of the programme.
- Participants with a traumatic fracture of one of the following sites: cervical, skull and face, hand and finger, toe, metatarsus, and patella.
- Pathological fracture.
- Women currently participating in a clinical trial requiring them to take a medication for osteoporosis.
Key Trial Info
Start Date :
June 1 2003
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2025
Estimated Enrollment :
2830 Patients enrolled
Trial Details
Trial ID
NCT00359047
Start Date
June 1 2003
End Date
December 1 2025
Last Update
November 21 2017
Active Locations (1)
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1
CHUdeQuebec, CHUL
Québec, Quebec, Canada, G1V 4G2