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Randomized Trial of Osteoporosis Intervention Strategies in Hip Fracture Patients

Randomized Trial of Osteoporosis Intervention Strategies in Hip Fracture Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00175175
Enrollment
220
Registered
2005-09-15
Start date
2002-03-31
Completion date
Unknown
Last updated
2006-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hip Fracture, Osteoporosis

Keywords

osteoporosis treatment, osteoporosis testing, hip fracture, quality improvement

Brief summary

Patients with hip fractures have suffered the most devastating consequence of osteoporosis; and yet, they are rarely if ever tested or treated for the condition, even though they remain at high risk of recurrent fracture. We hypothesize that, compared with usual care, an allied health professional-run osteoporosis service (case management) will be able to increase testing and treatment of osteoporosis in patients at high risk of fracture.

Detailed description

Patients with hip fractures have suffered the most devastating consequence of osteoporosis; and yet, they are rarely if ever tested or treated for the condition, even though they remain at high risk of recurrent fracture. We hypothesize that, compared with usual care, an allied health professional-run osteoporosis service (case management) will be able to increase testing and treatment of osteoporosis in patients at high risk of fracture.

Interventions

BEHAVIORALAllied health professional-run osteoporosis service (case-management)

Sponsors

Alberta Heritage Foundation for Medical Research
CollaboratorOTHER
Royal Alexandra Hospital
CollaboratorOTHER
University of Alberta
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* hip fracture patient \> 50 years of age * able to give consent (or proxy consent available) * lives within health region * no contraindications to bisphosphonate therapy

Exclusion criteria

* refuses to participate or consent * dementia or delirium without a proxy consent available * nursing home or longterm care * pathologic fracture * chronic glucocorticoid use * already receiving prescription osteoporosis treatment (calcium and vitamin D do not preclude inclusion)

Design outcomes

Primary

MeasureTime frame
The proportion of patients taking bisphosphonate therapy within 6 months of hip fracture

Secondary

MeasureTime frame
Proportion of patients taking prescription osteoporosis treatment at 6 months and 12 months
Proportion in receipt of a BMD test at 6 months and 12 months
Proportion still adherent to osteoporosis treatments at 6 months and 12 months
Proportion of patients with recurrent fractures at 6 months and 12 months
Cost effectiveness analyses

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 4, 2026