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Clinical Trials/NCT01112098
NCT01112098
Completed
N/A

Randomized Trial of a Mailed Intervention and Self-Scheduling to Improve Osteoporosis Screening in Postmenopausal Women

University of Alabama at Birmingham1 site in 1 country2,997 target enrollmentJuly 2008
ConditionsOsteoporosis

Overview

Phase
N/A
Intervention
Not specified
Conditions
Osteoporosis
Sponsor
University of Alabama at Birmingham
Enrollment
2997
Locations
1
Primary Endpoint
DXA scheduled
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

The purpose of this exploratory study is to test novel, mailed, low-cost, direct-to-patient intervention materials (i.e., a personalized letter and osteoporosis information pamphlet) designed to increase rates of dual energy X-ray absorptiometry (DXA) utilization and improve osteoporosis quality of care.

Detailed Description

While the occurrence of a fragility fracture (e.g. hip fracture) is indicative of low BMD and a clinical diagnosis of osteoporosis made, osteoporosis can be identified in asymptomatic patients using dual energy x-ray absorptiometry (DXA). United States (U.S.) guidelines recommend screening bone density tests using central DXA in all women 65 years or older. However, fewer than one-third of eligible U.S. women age 65 and older undergo DXA testing. The main barrier to achieving greater rates of osteoporosis screening is identifying a systematic, effective, and generalizable way for healthcare providers and patients to schedule DXA results. Given that national guidelines recommend DXA screening for all older women, the reasons a majority of women do not receive DXA testing are likely multifactorial. Patients and their health care providers may be unaware of preventative screening recommendations and the reasons for these recommendations. Screening tests that are required relatively infrequently (i.e. less than once a year) may be difficult for patients and physicians to remember if there are few triggers (e.g. seasonality as a trigger to motivate influenza vaccination). Additionally, primary care providers (PCPs) are responsible for managing a large number of comorbidities and acute care needs and may be unable to stay current with all preventative care needs during increasingly short clinic visits.

Registry
clinicaltrials.gov
Start Date
July 2008
End Date
April 2011
Last Updated
14 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Age 65 or older
  • At least one visit with a primary care physician in the previous 12 months

Exclusion Criteria

  • DXA scan in the previous 5 years

Outcomes

Primary Outcomes

DXA scheduled

Time Frame: 6 months

Patient scheduled a DXA within 6 months of receiving intervention materials

Study Sites (1)

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