View Clinical Trial (Medical Research Study)
Exercise-based Motivational Interviewing for Fibromyalgia - NCT00573612-46202(Clinical Trial 195176)
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Indianapolis |
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State:
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IN |
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46202 |
| Conditions: |
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Fibromyalgia |
| Purpose: |
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Fibromyalgia (FMS), defined as the presence of both chronic widespread pain and the finding
of 11/18 tender points on examination, affects 2% of the general population. Drug therapy
for FMS is largely symptomatic as there is not yet a complete understanding of the
pathogenesis of the disease. In the past 17 years, supervised aerobic exercise has emerged
as an important treatment modality to improve pain, aerobic capacity, function, and
well-being. Individuals who are able to adhere to exercise almost always maintain the
symptomatic benefits of exercise. Unfortunately, the rate of exercise adherence six months
after the completion of a well-structured supervised exercise program is disappointingly
low. Furthermore, although the efficacy of supervised aerobic exercise in the research
setting is well documented, the applicability of such intervention in the clinic setting is
doubtful. Therefore, we propose to conduct the Research to Encourage Exercise for
Fibromyalgia (REEF), a randomized attention-controlled trial whose primary aim is to
evaluate the efficacy of telephone-delivered motivational interviewing (MI) to encourage
exercise, in improving exercise adherence and self-report physical function (co-primary
outcome measures) for FMS patients. REEF will enroll 200 FMS patients, randomizing them to
either the MI group or the attention-control (AC) group. Participants from each group will
receive a total of 6 telephone calls within a 12-week period. Prior to the phone calls,
participants from both groups will receive an individualized exercise prescription and 2
supervised exercise training sessions to get them started on an exercise program. All
subjects will undergo comprehensive outcome assessment at baseline, week 12, week 24, and
week 36. The secondary aim of this proposal is to determine the mediators between MI and
improvement in self-report physical function. The proposed research is significant because
our focus is the promotion of adherence to an exercise program, of adequate intensity, in
order to maximize functioning and well-being for patients with FMS. The use of a
predominantly home-based exercise program and telephone-delivered MI by a trained licensed
practice nurse (LPN) could potentially make the proposed intervention more accessible to the
greater majority of FMS patients. Furthermore, if proven efficacious, MI could readily be
applied to other chronically painful conditions (e.g. chronic back pain).
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| Study summary: |
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| Criteria: |
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Inclusion Criteria:
1. American College of Rheumatology (ACR) classification criteria for FMS(203)
2. Has been on stable doses of FMS medications (i.e., cyclobenzaprine, tramadol,
gabapentin, pregabalin, venlafaxine, duloxetine, pramipexole, tricyclic
anti-depressant, selective serotonin reuptake inhibitor) for at least 4 weeks and
willing to limit the introduction of new medications for FMS symptoms
3. Age between 18-65 years old. Because the prevalence of sub-clinical coronary artery
disease increases with older age, we are excluding those who are ≥ 66 years old
Exclusion Criteria:
1. FIQ-PI score < 2
2. BPI-PS <4
3. Known cardiovascular disease, including congestive heart failure; previous episodes
of angina pectoris; previous myocardial infarction; or previous revascularization
procedure
4. Moderate-severe chronic obstructive pulmonary disease, including asthma
5. Uncontrolled hypertension
6. Orthopedic or musculoskeletal conditions that would prohibit moderate-intensity
exercise
7. Active suicidal ideation
8. Planned elective surgery during the study period
9. Ongoing unresolved disability claims
10. Other major rheumatic conditions (i.e. rheumatoid arthritis, systemic lupus
erythematosus, scleroderma and other connective tissue disease)
11. Use of medications that may affect chronotropic response to exercise, i.e.
beta-blocker or calcium channel blocker
12. Pregnancy
13. Schizophrenia or other psychosis
14. Exercising 3 days a week or more. The US Surgeon General considers a physically
active person as somebody who does at least 3 times a week of moderate to vigorous
level of exercise(204). Thus, we are excluding the already physically active
individuals from the study. In the pilot study, only 4% (2 out of 50) of the
potential participants were excluded due to being physically active. |
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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May 21, 2010 |
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