View Clinical Trial (Medical Research Study)
Nutrition and Coping Education for Symptom and Weight Management for Fibromyalgia - NCT00925431-84108(Clinical Trial 298682)
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Salt Lake City |
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State:
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UT |
| Zip Code: |
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84108 |
| Conditions: |
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Fibromyalgia - Obesity |
| Purpose: |
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Research has shown that weight problems are very common in fibromyalgia. Research also
suggests that overweight and obesity may contribute to worsening of fibromyalgia symptoms
and biochemical vulnerability associated with fibromyalgia. Effective weight management may
be important in not only improving general health but also better management of fibromyalgia
symptoms. Research has indicated that nutrition and coping education is important aspects of
successful weight management. In this study, the investigators are evaluating the effect of
nutrition and coping education on weight and symptom management of fibromyalgia among
overweight and obese patients.
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| Study summary: |
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| Criteria: |
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Inclusion Criteria:
- Fibromyalgia patients whose body mass index is greater than 25.
- Age 21-65 of both sex and all race.
Exclusion Criteria:
- Co-occurring progressive disease
- Planning to have surgery in the next year
- Pregnancy or planning to be pregnant in the next year
- Having known cardiovascular diseases
- Having known serious psychopathology (Diagnoses of psychosis, organic mental
disorder, dissociative disorder, active suicidal intent, inpatient admission to
psychiatric ward in the past year, evidence of self-injurious behaviors in the past
year, current or recent history (2years) of non-IV substance abuse, any history of
recreational IV drug use)
- Having autoimmune disorder (e.g., rheumatoid arthritis)
- Having neuropathic pain
- Having pain associated with terminal illness, acute pain, pain associated with
specific organ damage (eg, stomach ulcer)
- Concurrent use of weight controlling medications (eg, Xenical)
- A history of weight reduction surgery
- Concurrent participation in weight loss programs or other cognitive-behavioral coping
therapy
- Self-reported physician diagnosed conditions of chronic bronchitis, asthma, or
emphysema
- Report history of head injury, neurological illness, diagnosis of learning
disability, learning problems, or special education, substantial toxin or chemical
exposure within five years of FMS onset, near drowning, recreational IV drug use |
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| Study is available at: |
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Pain Research Center, University of Utah Salt Lake City, UT 84108 United States
Primary Contact: Mark Herrera Email: Mark.Herrera@hsc.utah.edu Phone: 801-585-7692
Secondary Contact: Reiko Mitsunaga, RN Email: pain.research@hsc.utah.edu Phone: 801-585-7695 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 23, 2011 |
Modifications to
this listing: |
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