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Improving Osteoporosis Care in High-Risk Home Health Patients - NCT00679198-35294(Clinical Trial 221246)



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City:  Birmingham
State:  
AL
Zip Code: 35294
Conditions: Patient Compliance - Communication - Osteoporosis - Fractures, Bone
Purpose: SPECIFIC AIMS: We propose a three-year study to develop a high-intensity intervention to improve osteoporosis care and test a novel intervention in a group-randomized trial of 27 home health offices and 1,000 patients referred to home health care with a history of fracture. Aim 1. Develop an intervention to promote osteoporosis treatment that includes: (1) training to enhance nurse-patient and nurse-physician risk communication regarding osteoporosis and fracture risk; (2) automated prompts within the home health agency's electronic medical record system to promote appropriate osteoporosis management; and (3) implementation of osteoporosis-related standardized care pathways and order sets. Aim 2. Conduct a group-randomized trial to test the effectiveness of the intervention to promote initial use of osteoporosis medications and adherence to treatment after discharge from home health. We hypothesize that: H1: Patients in the intervention group will have increased initial receipt of osteoporosis prescription medications and calcium/vitamin D supplements to prevent and treat osteoporosis compared to patients receiving usual care; H2: Patients in the intervention group will demonstrate increased persistence in the use of these therapies compared to those receiving usual care. Secondary Aims (SA) will include exploratory analyses of fracture related morbidity and mortality, patient-reported quality of life, and health services utilization and costs.
Study summary:
Criteria: Inclusion Criteria: - Patients will be identified as "at-risk" if they are referred to home health care for post-fracture care or if they are admitted for another reason and have a previous diagnosis of fracture. Exclusion Criteria: - Patients in hospice, with a life expectancy < 1 year, over 95 years old, or with concomitant metabolic bone diseases (e.g. Paget's disease of bone) will be excluded.
Study is available at: University of Alabama at Birmingham Department of Rheumatology
Birmingham, AL 35294
United States

Primary Contact:
Meredith L Kilgore, PhD RN
Email: MKilgore@ms.soph.uab.edu

Secondary Contact:
Meredith L Kilgore, PhD RN
Email: MKilgore@ms.soph.uab.edu
Phone: (205) 975-8840
If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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Data Source: ClinicalTrials.gov
Date Processed: March 22, 2011
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