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N/A Completed N=7,749 Randomized Double-blind Health Services Research

Patient Activation After DXA Result Notification

Osteoporosis · Bone Diseases, Metabolic
Source: ClinicalTrials.gov NCT01507662 ↗
Enrolled (actual)
7,749
Serious AEs
Results posted
Apr 2017
Primary outcomePrimary: Guideline Concordant Osteoporosis Therapy — 2537; 2477 Participants

Summary

There is growing evidence that patients undergoing bone mineral density testing (BMD) often do not take important steps to improve their bone health. The investigators will conduct a randomized-controlled trial to evaluate the impact of a novel and practical patient activation intervention (mailing patients their bone density test results) on the quality of bone-related healthcare and the cost-effectiveness of BMD testing. Equally important, the investigators intervention could easily be modified to include other patient populations and chronic diseases.

Outcome Measures

OutcomeResultp-value
PRIMARY
Guideline Concordant Osteoporosis Therapy
2537; 2477

Eligibility Criteria

Inclusion Criteria

  • patients presenting for DXA
  • age 50 years of age or older

Exclusion Criteria

  • non-English speakers
  • prisoners
  • people who have mental disabilities
  • individuals younger than age 50 years
  • individuals who do not have access to a telephone
  • deaf patients
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01507662). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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