![]() |
Home
Search
Study Topics
Glossary
|
![]() |
![]() |
![]() |
|
![]() |
|
![]() |
|
![]() |
|
![]() |
![]() |
![]() |
|
![]() |
Sponsors and Collaborators: |
Centers for Disease Control and Prevention West Virginia University |
---|---|
Information provided by: | Centers for Disease Control and Prevention |
ClinicalTrials.gov Identifier: | NCT00526201 |
The purpose of this project is to determine if an evidence-based, community-delivered physical activity program, EnhanceFitness, yields benefits for participants with arthritis. The 3-year project will: 1) conduct a meta-analysis of community-based exercise programs for adults, 2) implement and evaluate the EnhanceFitness program in West Virginia using a randomized, controlled (wait list) design, and 3) disseminate the results to community and public health partners. It is anticipated that participation in the EnhanceFitness program will result in reduced pain, improved physical function and physical activity levels for adults with arthritis.
Condition | Intervention | Phase |
---|---|---|
Arthritis |
Behavioral: 12-weeks EnhanceFitness Behavioral: Control |
Phase III |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Open Label, Placebo Control, Parallel Assignment, Safety/Efficacy Study |
Official Title: | Arthritis Benefits of a Physical Activity Program in West Virginia: Evaluation of EnhanceFitness |
Estimated Enrollment: | 375 |
Study Start Date: | May 2008 |
Estimated Study Completion Date: | May 2009 |
Estimated Primary Completion Date: | December 2008 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
---|---|
Exercise: Experimental
Subjects will be randomized to exercise (12 week EnhanceFitness class) or a wait-list control group.
|
Behavioral: 12-weeks EnhanceFitness
EnhanceFitness class for 12 weeks, 3 times per week for 1 hour sessions.
|
Control: No Intervention
Wait-list control group will receive intervention after 12-weeks.
|
Behavioral: Control
Participants randomized to the wait-list control group will continue their regular activities for 12 weeks and then be offered the exercise intervention (EnhanceFitness).
|
Ages Eligible for Study: | 18 Years to 85 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Dina L Jones, PhD, PT | 304-293-1078 | djones@hsc.wvu.edu |
Contact: Jeanne M Goodman, MPA | 304-293-9255 | jmgoodman@hsc.wvu.edu |
United States, West Virginia | |
West Virginia University | |
Morgantown, West Virginia, United States, 26506-9196 |
Principal Investigator: | Dina L Jones, PT, PHD | West Virginia University |
Study Director: | Jennifer M Hootman, PhD | Centers for Disease Control and Prevention |
Responsible Party: | West Virginia University ( Dina L. Jones PT, PHD ) |
Study ID Numbers: | CDC-NCCDPHP-AAMC-0944, AAMC-0944 |
Study First Received: | September 6, 2007 |
Last Updated: | July 31, 2008 |
ClinicalTrials.gov Identifier: | NCT00526201 |
Health Authority: | United States: Federal Government |
Arthritis Osteoarthritis Rheumatoid Arthritis Fibromyalgia Lupus |
Musculoskeletal Diseases Myofascial Pain Syndromes Fibromyalgia Osteoarthritis |
Joint Diseases Arthritis Arthritis, Rheumatoid |