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Self-Directed Exercise Program for Adults With Arthritis

Evaluation of a Self-directed, Packaged Physical Activity Program for Adults With Arthritis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01172327
Enrollment
401
Registered
2010-07-29
Start date
2009-09-30
Completion date
2012-07-31
Last updated
2021-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthritis, Osteoarthritis, Rheumatoid Arthritis, Fibromyalgia

Brief summary

The purpose of this study is to examine the effectiveness and safety of a self-directed physical activity program relative to a self-directed dietary program in adults with arthritis. A process evaluation will also be conducted to examine program reach, participation/dose, fidelity, and participant compatibility/satisfaction.

Detailed description

Physical activity is a critical component of arthritis disease management. It also reduces the risk for other chronic comorbid conditions in people with arthritis. Yet, most adults with arthritis are not sufficiently active at the level needed to achieve benefits. Existing group-based arthritis exercise programs reach only a very small percentage of the population. The overall purpose of this study is to test a self-directed and low-cost multicomponent physical activity program for people with arthritis on outcomes including symptoms of arthritis, lower body strength, functional aerobic capacity, flexibility, physical activity, arthritis self-efficacy and disability, upper body strength, balance, gait, and depressive symptoms. The second primary aim is to evaluate the safety of the physical activity program. The third primary aim is to conduct a process evaluation to examine program reach, participation/dose, fidelity, and participant compatibility/satisfaction. Adults aged 18 years and older with arthritis will be recruited from the midlands area of South Carolina. After completion of a baseline visit, participants will be randomized in equal numbers to the 12-week physical activity program (First Step to Active Health®) or the 12-week attention-control group (Steps to Healthy Eating). The attention control intervention will have the same look and feel as the physical activity intervention and will require similar activities such as self-monitoring of behavior. Follow-up measurements will take place post-program (12-weeks) and 6 months post-program (i.e., 9 months post-randomization). If First Step to Active Health® is shown to be effective, it could be widely disseminated for a very low cost, thus having the potential to make a tremendous public health impact on the burden of arthritis.

Interventions

This intervention is a self-directed, multicomponent, exercise intervention. Participants exercise on their own and follow a progressive stepped program that occurs in the following order: cardiorespiratory exercises, flexibility exercises, strength (upper and lower body) exercises, and balance exercises. Participants also complete a daily log of their exercises and return the logs every week for 12 weeks. The active intervention phase is 12 weeks.

BEHAVIORALNutrition

This arm is a self-directed nutrition intervention. Participants follow a progressive stepped program that occurs in the following order: fruits, vegetables, grains, meat and beans. Participants also complete a daily log of their dietary intake and return the logs every week for 12 weeks. The active intervention lasts for 12 weeks.

Sponsors

Centers for Disease Control and Prevention
CollaboratorFED
University of South Carolina
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Self-reported, health care provider-diagnosed arthritis (CDC definition) * 18+ years of age * Self-reported symptoms of joint pain, stiffness, tenderness, decreased range of motion, redness and warmth, deformity, crackling or grating, or fatigue * Able to read and write in English

Exclusion criteria

* Another member of household is participating in study * Plans to move from the Columbia, SC area in the next 9 months * Unable to walk longer than 3 minutes without taking a rest * Unable to stand without assistance for more than 2 minutes * Cannot sit in a chair without arms for more than 5 minutes * Measured resting blood pressure \>160/100 * Positive response to PAR-Q question(s) * Had a fall in the past year that required medical assistance * Pregnant or breastfeeding * Uses insulin to manage diabetes * Participating in another research study that includes an intervention or drug * Participates in 3+ days of structured moderate-intensity exercise for 30+ minutes per day * Participates in 2+ days of strength building exercises for 20+ minutes per day

Design outcomes

Primary

MeasureTime frameDescription
Arthritis management self-efficacy12 weeksThe Arthritis Self-Efficacy Scale will assess confidence in managing arthritis symptoms
Symptoms of arthritis12 weeksVisual numeric scales to assess pain, fatigue, and stiffness
Lower body strength12 weeksThe 30-second chair stand will assess lower body strength.
Functional exercise capacity12 weeksThe six-minute walk will assess functional exercise capacity
Flexibility12 weeksThe sit-and-reach test will assess flexibility
Physical activity12 weeksThe Community Health Activities Model Program for Seniors Physical Activity (CHAMPS) Questionnaire will assess physical activity participation

Secondary

MeasureTime frameDescription
Upper body strength12 weeksThe grip strength test (kg/lbs of force) will assess upper body strength
Balance12 weeksPostural sway will be measured with the AMTI force platform to determine COP displacement, COP velocity, and 95th eclipse
Gait12 weeksGAITRite will assess components of gait including cadence, step time, cycle time, step length, stride length, and velocity
Depressive symptoms12 weeksThe short form of the Center for Epidemiological Studies Depression scale (CES-D) will assess depressive symptoms
Disability12 weeksThe Health Assessment Questionnaire (HAQ) will assess disability

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 19, 2026