Improving Management of Patients at High Risk for Osteoporotic Fractures (0000-038)

NCT ID: NCT00139438

Last Updated: 2016-04-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

4266 participants

Study Classification

INTERVENTIONAL

Study Start Date

2004-09-30

Study Completion Date

2005-06-30

Brief Summary

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The purpose of this study is to assess the impact of disease management interventions on percent receiving a bone densitometry test and percent appropriately prescribed a medication for osteoporosis.

Detailed Description

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Conditions

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Osteoporosis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Blinding Strategy

NONE

Interventions

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Disease Management Assessment

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Members of the Horizon Blue Cross Blue Shield of New Jersey who are at risk for osteoporosis based on age (women age 65 or older, men and women age 45 or older who have a history of fragility fracture or have a history of taking oral glucocorticoids over 3 months).
Minimum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Merck Sharp & Dohme LLC

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Daniel H. Solomon, M.D., M.P.H.

Role: PRINCIPAL_INVESTIGATOR

Brigham and Woman's Hospital

Other Identifiers

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038

Identifier Type: -

Identifier Source: secondary_id

2005_049

Identifier Type: -

Identifier Source: secondary_id

0000-038

Identifier Type: -

Identifier Source: org_study_id

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