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Trial of a Physical Activity Intervention for RA Fatigue

Randomized Controlled Trial of a Physical Activity Intervention for RA Fatigue

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01874977
Enrollment
96
Registered
2013-06-11
Start date
2013-11-30
Completion date
2016-03-31
Last updated
2016-05-12

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

Conditions

Rheumatoid Arthritis

Keywords

rheumatoid arthritis, fatigue, physical activity

Brief summary

The major goal of this project is to conduct a randomized, controlled trial of the impact of a practical, low cost physical activity intervention on fatigue among persons with rheumatoid arthritis (RA). Fatigue has been identified as a major concern for individuals with RA, and is considered a core outcome measure for RA. Our recent study of the sources of fatigue identified physical inactivity as a primary predictor of fatigue. Studies have examined the impact of exercise interventions on RA outcomes, but most of these interventions have focused on pain or function as outcomes. The few exercise studies examining fatigue suggest that increasing physical activity reduces fatigue, but the interventions have been resource-intensive, requiring specially trained personnel to administer them, highly structured activities, and/or attendance at classes or a specified facility. Each of these components increases the cost and barriers to implementation of an intervention. Pedometers have been shown to be an effective means of increasing physical activity, and could form the basis of a simple means to increase physical activity. This project will test the effect of a simple pedometer-based intervention, with two incremental degrees of guidance, on increasing physical activity and decreasing fatigue. Three groups (n=40 in each) will be studied: a control group with an educational pamphlet only, a pedometer-only intervention group, and a pedometer group with step targets. Both intervention groups will keep step-count diaries. Groups will be followed over 20 weeks. We expect that (1) the pedometer-only intervention group will increase activity more than the education group, and the group with step-count targets will demonstrate even greater increases in activity; and (2) greater increases in activity will be associated with greater decreases in fatigue. Secondary outcome measures will include depressive symptoms, self-reported sleep quality, and body composition. Our overall goal is to demonstrate an effective, yet simple and low cost, physical activity intervention to decrease fatigue that could be broadly accessible and have the potential for wide implementation.

Interventions

BEHAVIORALPedometer

Will receive the educational booklet and discussion, plus a pedometer and a diary to record their daily step counts from the pedometer.

BEHAVIORALEducational materials

Will receive the educational booklet (Be Active Your Way: A guide for Adults; http://www.health.gov/paguidelines/adultguide/default.aspx).and a discussion of simple ways to increase physical activity in daily life based on the booklet, following the baseline assessment.

BEHAVIORALStep count goals

Will receive the educational booklet and discussion, and the pedometer and step diary, plus will be given individualized daily step targets.

Sponsors

University of California, San Francisco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* Physicians' diagnosis of RA * English verbal fluency * Residence in the greater San Francisco Bay Area * Score ≥20 on 10-item PROMIS fatigue scale, or at least one item rated often * BMI ≥ 20 kg/m2

Exclusion criteria

* Currently engaging in regular exercise * Non-ambulatory or presence of a condition or comorbid disease that would limit the ability to engage in walking (e.g., foot deformities, lower extremity joint surgery upcoming or in past 6 months, myocardial infarction in past 6 months, stroke, congestive heart failure, severe chronic obstructive pulmonary disease).

Design outcomes

Primary

MeasureTime frame
PROMIS Fatigue scalechange from baseline fatigue score at 20 weeks

Secondary

MeasureTime frameDescription
Patient Health Questionnaire-9 (PHQ-9)change from baseline PHQ-9 score at 20 weeksdepressive symptoms
Pittsburg Sleep Quality Index (PSQI)Change from baseline PSQI score at 20 weeksself-reported sleep quality
Change in weightChange from baseline weight at 20 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026