Improving Functional Recovery After Hip Fracture
Completed · Phase 3
Conditions studied: Unilateral Hip Fracture
In brief
This project will assess the effectiveness of a novel approach involving patient education and strength training to improve functional recovery after a hip fracture. Participants will be randomly assigned to one of two study groups. One group (control group) will receive standard medical care. The other group will participate in a program of patient education and strength training, including an at-home walking program.
Key facts
- Study ID
- NCT00000436
- Run by
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
- People needed
- 200
- Starts
- 1993-07-01
- Expected to finish
- 2000-06-01
- Last updated by the study team
- 2007-01-04
Who can join
Age: 65 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients who are 65 years of age and older, and who have been admitted for a hip fracture to the Fracture Service at New York Presbyterian Hospital.
You may not qualify if…
- Patients who are unable to give informed consent on the 4th or 5th day after surgery.
- Patients whose hip fracture is due to underlying disease, secondary to malignancy (cancer).
- Patients who do not speak English.
- Patients for whom exercise is contraindicated or whose physicians believe that exercise is contraindicated.
- Patients who do not have access to a telephone or cannot be reached by telephone.
- Patients and physicians who refuse to participate or who intend to relocate upon discharge.
Where it is running
- Hospital for Special Surgery — New York, New York, United States
Full record on ClinicalTrials.gov
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