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Osteoporosis Disease Management Demonstration Project
This study is ongoing, but not recruiting participants.
Sponsored by: Merck
Information provided by: Merck
ClinicalTrials.gov Identifier: NCT00139425
  Purpose

The purpose of this study is to assess the impact of disease management interventions on bone mineral density (BMD) screening rates and osteoporosis treatment rates in women age 65 years or older.


Condition Intervention
Osteoporosis
Behavioral: Disease Management Assessment

MedlinePlus related topics: Minerals Osteoporosis
U.S. FDA Resources
Study Type: Interventional
Study Design: Educational/Counseling/Training, Randomized, Open Label, Placebo Control, Parallel Assignment
Official Title: Osteoporosis Prevention and Treatment Program: A Disease Management Demonstration Project

Further study details as provided by Merck:

Primary Outcome Measures:
  • Bone mineral density (BMD) testing rates

Secondary Outcome Measures:
  • Osteoporosis medication treatment rates

Estimated Enrollment: 10000
Study Start Date: May 2003
  Eligibility

Ages Eligible for Study:   65 Years to 89 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Members of the Henry Ford Health System

Exclusion Criteria:

  • Individuals who are not members of the Henry Ford Health System
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00139425

Sponsors and Collaborators
Merck
Investigators
Study Director: Medical Monitor Merck
  More Information

Publications indexed to this study:
Study ID Numbers: 2005_048
Study First Received: August 29, 2005
Last Updated: September 7, 2005
ClinicalTrials.gov Identifier: NCT00139425  
Health Authority: United States: Institutional Review Board

Study placed in the following topic categories:
Musculoskeletal Diseases
Osteoporosis
Bone Diseases, Metabolic
Bone Diseases

ClinicalTrials.gov processed this record on January 16, 2009