Randomized Trial of Osteoporosis Intervention Strategies in Hip Fracture Patients

Sponsor
University of Alberta (Other)
Overall Status
Completed
CT.gov ID
NCT00175175
Collaborator
Alberta Heritage Foundation for Medical Research (Other), Royal Alexandra Hospital (Other)
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Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Allied health professional-run osteoporosis service ("case-management")
N/A

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.

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single
Primary Purpose:
Treatment
Official Title:
Randomized Trial of Osteoporosis Intervention Strategies in Hip Fracture Patients
Study Start Date :
Mar 1, 2002

Outcome Measures

Primary Outcome Measures

  1. The proportion of patients taking bisphosphonate therapy within 6 months of hip fracture []

Secondary Outcome Measures

  1. Proportion of patients taking prescription osteoporosis treatment at 6 months and 12 months []

  2. Proportion in receipt of a BMD test at 6 months and 12 months []

  3. Proportion still adherent to osteoporosis treatments at 6 months and 12 months []

  4. Proportion of patients with recurrent fractures at 6 months and 12 months []

  5. Cost effectiveness analyses []

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years and Older
Sexes Eligible for Study:
All
Accepts 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)

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Alberta Hospitals Edmonton Alberta Canada T6G 2B7

Sponsors and Collaborators

  • University of Alberta
  • Alberta Heritage Foundation for Medical Research
  • Royal Alexandra Hospital

Investigators

  • Principal Investigator: Sumit R Majumdar, MD, MPH, University of Alberta

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00175175
Other Study ID Numbers:
  • AHFMR #200100791
First Posted:
Sep 15, 2005
Last Update Posted:
Sep 15, 2006
Last Verified:
Sep 1, 2006

Study Results

No Results Posted as of Sep 15, 2006