Development and Evaluation of A Mailed Arthritis Self-Management Program
Mail-Delivered Arthritis Self-Management Education -- Years 1, 2, Carryover
1 other identifier
interventional
900
1 country
1
Brief Summary
The purpose of this study is twofold, to develop and test the effectiveness of a mailed arthritis self-management education intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Nov 2005
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2005
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2006
CompletedFirst Submitted
Initial submission to the registry
March 14, 2007
CompletedFirst Posted
Study publicly available on registry
March 16, 2007
CompletedMarch 16, 2007
March 1, 2007
March 14, 2007
March 15, 2007
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Health-related Quality of Life (Self-reported Health, Pain, Disability, Fatigue, Activity Limitation, Health Distress)
Health Care Utilization
Self-Management Behaviors
Self-Efficacy for Arthritis Self-Management
Interventions
Eligibility Criteria
You may qualify if:
- Report MD diagnosis of osteoarthritis or rheumatoid arthritis, or meet CDC criteria for chronic joint symptoms
- Are at least 18 years of age
- Are able to complete informed consent, enrollment forms, and interviews/questionnaires
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of North Carolinalead
- Stanford Universitycollaborator
- Centers for Disease Control and Preventioncollaborator
Study Sites (1)
University of North Carolina at Chapel Hill
Chapel Hill, North Carolina, 27599, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jean Goeppinger, PhD, BSN
University of North Carolina, Chapel Hill
- PRINCIPAL INVESTIGATOR
Kate Lorig, DrPH, BSN
Stanford University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- ECT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
March 14, 2007
First Posted
March 16, 2007
Study Start
November 1, 2005
Study Completion
July 1, 2006
Last Updated
March 16, 2007
Record last verified: 2007-03