Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT00594789

Closing The Post Fracture Care Gap In Manitoba

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
4,264 (actual)
Sponsor
University of Manitoba · Academic / Other
Sex
All
Age
50 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to evaluate a post-fracture intervention for improving osteoporosis care in older men and women who have suffered a fracture that may indicate the presence of osteoporosis. Although osteoporosis can be identified with a bone mineral density (BMD) test, most individuals with osteoporosis are not diagnosed until they fracture. Post-fracture care often "falls between the cracks" when there is a breakdown in communication between hospital and community, or between specialists and primary care physicians. Often physicians and patients fail to make the connection between an acute fracture and osteoporosis, or the value of secondary prevention strategies. If untreated, there is an extremely high rate of additional fractures after a first osteoporotic fracture. It follows that improving BMD testing and/or treatment in appropriately identified individuals is a necessary step in optimizing post-fracture patient care. Over the next three years we will be testing and optimizing a notification procedure to physicians and/or patients relying upon fracture events reported to the provincial health service (Manitoba Health).

Detailed description

A major 'care gap' exists in the management of patients with fractures suggestive of osteoporosis. Currently, only a small minority of these individuals who are at high risk for recurrent fractures undergo evaluation for possible treatment. We propose to test and optimize a novel approach to address this question, relying upon fracture events reported to provincial health service (Manitoba Health) as a mechanism for osteoporosis case identification and enhancing post fracture care. Phase 1 (one year duration): individuals meeting the fracture case definition will be randomized to usual care (no intervention), physician notification and physician/patient notification. The notification will provide a general recommendation for osteoporosis assessment. The use of appropriate post-fracture investigations and treatment will be prospectively evaluated. Phase 2 (up to two years duration): the intervention will be refined and iteratively trialed for all individuals meeting the fracture case definition. Phase 3: a recommendation for long term maintenance of the post-fracture intervention will be developed.

Conditions

Interventions

TypeNameDescription
OTHERInformation lettersInformation letters under Manitoba Health letterhead will be sent out to physician(s) and/or patient connected with a fracture that meets specific criteria. To address concerns over discontinuous care of patient seen at the time of fracture and for subsequent follow-up, the physician notification will specifically target the individual involved in the initial report to Manitoba Health as well as the primary care physician (using an algorithm developed by the Manitoba Centre for Health Policy). The notification will provide a general recommendation for osteoporosis assessment in addition to a copy of the BMD testing requisition since BMD testing is usually justified in this setting. The notification will not dictate what testing or treatment needs to be performed.

Timeline

Start date
2008-06-01
Primary completion
2011-03-01
Completion
2028-12-01
First posted
2008-01-16
Last updated
2025-03-28

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00594789. Inclusion in this directory is not an endorsement.

Closing The Post Fracture Care Gap In Manitoba (NCT00594789) · Clinical Trials Directory