Study Results
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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COMPLETED
PHASE3
191 participants
INTERVENTIONAL
1997-01-31
2002-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Active coaching
Telephone and in person coaching
Coaching, providing social support
Active telephone and in person coaching
Usual care
Return to PCP for usual care
Coaching, providing social support
Active telephone and in person coaching
Interventions
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Coaching, providing social support
Active telephone and in person coaching
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
ALL
No
Sponsors
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Washington University School of Medicine
OTHER
Responsible Party
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Washington University School of Medicine
Principal Investigators
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Robert Strunk, MD
Role: PRINCIPAL_INVESTIGATOR
Washington University School of Medicine
Locations
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Washington University School of Medicine
St Louis, Missouri, United States
Countries
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Other Identifiers
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ES08711
Identifier Type: -
Identifier Source: org_study_id
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