Arthritis Self-Management Education Program
2 other identifiers
interventional
690
1 country
2
Brief Summary
We will develop brief versions of the classic 6-week Arthritis Self-Management Program and evaluate their effectiveness.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Oct 2006
Typical duration for not_applicable
2 active sites
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
October 1, 2006
CompletedFirst Submitted
Initial submission to the registry
April 25, 2007
CompletedFirst Posted
Study publicly available on registry
April 27, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2007
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2008
CompletedJanuary 28, 2010
January 1, 2010
1.2 years
April 25, 2007
January 27, 2010
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Self-Efficacy
10-1-05-9-30-09
Secondary Outcomes (1)
Self-reported health
10-1-05-9-30-09
Study Arms (2)
Arthritis self-management workshop
EXPERIMENTALComparison of two-week, lay led, scripted self-management workshop emphasizing action planning, problem-solving, and content specific to arthritis.
Delayed treatment control
OTHERAfter 4 month delay, participants in Control Group receive Experimental intervention.
Interventions
Two week, lay led, workshop focusing on goal setting, problem solving, and content specific to disease management.
After four months delay, participants in Control Group receive Experimental workshop.
Eligibility Criteria
You may qualify if:
- Adults, 18 years or older
- Arthritis diagnosis
- No prior participation in arthritis self-management
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of North Carolina, Chapel Hilllead
- Stanford Universitycollaborator
- Centers for Disease Control and Preventioncollaborator
Study Sites (2)
Stanford University Patient Education Research Center
Palo Alto, California, 94304, United States
University of North Carolina Center for Health Promotion & Disease Prevention
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
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
April 25, 2007
First Posted
April 27, 2007
Study Start
October 1, 2006
Primary Completion
December 1, 2007
Study Completion
December 1, 2008
Last Updated
January 28, 2010
Record last verified: 2010-01