Program Evaluation of People With Arthritis Can Exercise
Evaluation of the Health Benefits of the People With Arthritis Can Exercise Program
2 other identifiers
interventional
320
1 country
1
Brief Summary
The purpose of this study is to evaluate the health and arthritis-specific benefits of participation in the Arthritis Foundation People with Arthritis Can Exercise program and to collect information to improve community-based dissemination of this program.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_2
Started Jun 2003
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
June 1, 2003
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2005
CompletedFirst Submitted
Initial submission to the registry
September 7, 2005
CompletedFirst Posted
Study publicly available on registry
September 12, 2005
CompletedNovember 17, 2005
September 1, 2005
September 7, 2005
November 16, 2005
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Physical Activity Level - PASE instrument at baseline, 8 and 16 weeks.
Pain Visual Analog Scale - at baseline, 8 and 16 weeks
Physical Function using the Functional Fitness Battery at baseline, 8 and 16 weeks
Self-reported function (HAQ) at baseline, 8 and 16 weeks
Secondary Outcomes (7)
Health-related quality of life
Disease status
Self-efficacy for arthritis management
Self-efficacy for exercise
Social support
- +2 more secondary outcomes
Interventions
Eligibility Criteria
You may qualify if:
- Adults age 18 and older
- Self-reported arthritis or chronic joint symptoms
- Community-dwelling
You may not qualify if:
- Serious medical conditions which would contraindicate exercise
- No severe physical or mental condition
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Centers for Disease Control and Preventionlead
- University of Missouri-Columbiacollaborator
- St. Louis Universitycollaborator
Study Sites (1)
St. Louis University
St Louis, Missouri, 63104, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Jennifer M Hootman, PhD
Centers for Disease Control and Prevention
- PRINCIPAL INVESTIGATOR
Marian Minor, PhD
University of Missouri-Columbia
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- FED
Study Record Dates
First Submitted
September 7, 2005
First Posted
September 12, 2005
Study Start
June 1, 2003
Study Completion
June 1, 2005
Last Updated
November 17, 2005
Record last verified: 2005-09