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Clinical Trials/NCT00226031
NCT00226031
Completed
Not Applicable

Optimal Management of Older Women With Distal Forearm Fractures

Queen's University1 site in 1 country270 target enrollmentSeptember 2003

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Osteoporosis
Sponsor
Queen's University
Enrollment
270
Locations
1
Primary Endpoint
Proportion of women who are prescribed anti-osteoporosis therapy within 6 months of sustaining a forearm fracture.
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

To evaluate the effectiveness of a multifaceted intervention (reminder and educational material) in improving the evaluation of osteoporosis follow-up care of post-menopausal women with wrist fractures by their primary care physicians. The intervention is directed at improving the gap in continuity of care between emergency/fracture clinics and family physicians, and reducing knowledge gaps.

Detailed Description

Numerous studies have demonstrated that women with wrist fractures have lower bone mineral density. Despite new guidelines for the care of such women, research has shown that they are not generally evaluated for osteoporosis. This care gap exists although it is known that wrist fractures are an important marker for subsequent fractures, such as a hip fracture, which represents a significant socio-economic burden to society. Comparison: Cluster randomized trial of women and their physicians, both of whom receive educational material and reminder on post fracture osteoporosis evaluation. Comparison is to women and their physicians who receive standard post fracture information. Family practices are randomized to intervention or non-intervention group.

Registry
clinicaltrials.gov
Start Date
September 2003
End Date
August 2007
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Postmenopausal women with low trauma distal radius fracture (confirmed by x-ray).
  • Can be taking Didrocal (etidronate), Miacalcin (calcitonin),or hormone replacement therapy .

Exclusion Criteria

  • Women with fractures of the elbow, mid radius, scaphoid, or injury to wrists (without actual fracture).
  • Significant cognitive impairment (which would preclude them from filling out simple questionnaires).
  • Women already taking osteoporosis therapy, ie. either Fosamax (alendronate), Actonel (risedronate), or the selective estrogen receptor modulator, Evista (raloxifene).

Outcomes

Primary Outcomes

Proportion of women who are prescribed anti-osteoporosis therapy within 6 months of sustaining a forearm fracture.

Time Frame: 6 months

Secondary Outcomes

  • Proportion of women in whom a bone density scan is ordered and the proportion of women who receive counseling advice about osteoporosis from their family physicians.(6 months)
  • Women's knowledge about osteoporosis and fractures (Osteoporosis Knowledge Questionnaire).(6 months)

Study Sites (1)

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