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Arthritis Self-Management Education Program
This study is currently recruiting participants.
Study NCT00467064   Information provided by The University of North Carolina, Chapel Hill
First Received: April 25, 2007   Last Updated: April 26, 2007   History of Changes

April 25, 2007
April 26, 2007
October 2006
 
  • Self-Management Behaviors
  • Arthritis Self-Efficacy
  • Health-related Quality of Life (Self-reported Health, Pain, Disability, Fatigue, Activity Limitation, and Health Distress
  • Health Care Utilization
Same as current
Complete list of historical versions of study NCT00467064 on ClinicalTrials.gov Archive Site
 
 
 
Arthritis Self-Management Education Program
Arthritis Self-Management Education -- Dose Response

We will develop brief versions of the classic 6-week Arthritis Self-Management Program and evaluate their effectiveness.

Many national statements have been made recently about the importance of evidence-based arthritis self-management to improvements in the public’s health. The prevalence of arthritis is increasing as the US population ages; the prevalence of arthritis-related disability is higher among Blacks than Whites. Effective arthritis self-management education programs with varying formats have been developed and found effective. Despite this, many Arthritis Foundation chapters and arthritis units of state health departments have found dissemination difficult, and cite the time demands (6 weekly sessions, 2 hours/session) of the classic arthritis self-management education program (ASMP) as a major barrier. Researchers at the University of North Carolina at Chapel Hill and Stanford University will develop and evaluate two “low dose” arthritis self-management programs. The study will be conducted in three phases. Phase One (Development): Researchers will conduct needs assessments with arthritis self-management program disseminators, rheumatologists and other arthritis health professionals, and potential program users to determine preferred content, length, and schedule. Using findings from these assessments, researchers will develop two “low dose” versions of the ASMP. Phase Two (Implementation and Evaluation): Researchers will evaluate the “response” (effectiveness) of both “low dose” interventions in a randomized controlled trial (4 months) and a longitudinal study (one year). We will measure four outcomes: (1) Self-Management Behaviors, (2) Arthritis Self-Efficacy, (3) Health-related Quality of Life (Self-reported Health, Pain, Disability, Fatigue, Activity Limitation, and Health Distress); and (4) Health Care Utilization. A sample of 700 adults with diagnosed arthritis or chronic joint pain, including 200 African Americans, will participate in the study. All data will be gathered via self-administered mailed questionnaires, with telephone follow-up as needed. We will use analysis of co-variance and structural equation modeling to evaluate effectiveness. Researchers will also compare the effectiveness of each new “low dose” program with the effectiveness of existing arthritis self-management education program options. Phase Three (Dissemination): We will consult with arthritis units of state health departments and state chapters of the Arthritis Foundation on program adoption and distribution.

 
Interventional
Other, Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study
Arthritis
Behavioral: Arthritis Self-Management Education Workshop
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
700
July 2008
 

Inclusion Criteria:

  • Adults, 18 years or older
  • Arthritis diagnosis
  • No prior participation in arthritis self-management
Both
18 Years and older
Yes
Contact: Jean Goeppinger, PhD, BSN 919-832-2213 jgoeppin@email.unc.edu
United States
 
NCT00467064
 
06-0398-1-3
University of North Carolina
  • Stanford University
  • Centers for Disease Control and Prevention
Principal Investigator: Jean Goeppinger, PhD, BSN The University of North Carolina, Chapel Hill
Principal Investigator: Kate Lorig, DrPH, BSN Stanford University
The University of North Carolina, Chapel Hill
April 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP