Osteoporosis Choice Decision Aid for Use of Bisphosphonates in Postmenopausal Women
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Details and patient eligibility
About
To develop a decision aid to support the decision to use (or not use) bisphosphonates in postmenopausal women at risk for osteoporotic fractures, and to assess the impact of the decision aid on start and six month adherence to bisphosphonates.
Full description
Bisphosphonates can reduce fracture risk in patients with osteoporosis. However, many patients may not start and adhere to bisphosphonates, consequently losing independence, quality, and length of life. We hypothesize that a decision aid that efficiently improves patient education and communication with their provider about fracture risk, and about using bisphosphonates to reduce that risk, will improve the quality of treatment decisions. We anticipate that patients will become more involved in the decision-making process and decisions will be more consistent with patients' values and health care goals. We expect this will lead to increased bisphosphonate start and adherence and improved patient outcomes.
Enrollment
Sex
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Volunteers
Inclusion criteria
- Female, post-menopausal women aged 50 to 90.
- Have a bone mineral density (BMD) evaluation resulting in a T-Score of <-1.0.
- Have a follow-up appointment with a provider in the areas of Family Medicine (FM), Primary Care Internal Medicine (PCIM), or POM.
- Have no major barriers (i.e., severe hearing impairment, dementia, require interpreter, etc.) to participation in shared decision-making (per provider's assessment)
- Enrollment is open to females of diverse racial backgrounds.
Exclusion criteria
- Currently taking a bisphosphonate.
- Not available for 6 month follow-up phone call.
Trial design
100 participants in 2 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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