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Completed

NCT Number: NCT01420640

Tai Chi and Aerobic Exercise for Fibromyalgia (FMEx)

The investigators will conduct a large randomized controlled trial comparing the effectiveness of Tai Chi mind-body exercise and standard-of-care aerobic exercise for fibromyalgia. In addition, the investigators will determine the optimal frequency and duration of a Tai Chi intervention for short and long-term effectiveness.

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Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Tufts Medical Center

Boston, Massachusetts, 02111, United States

About this study

Fibromyalgia (FM) is a chronic musculoskeletal pain syndrome that causes substantial physical and psychological impairment and costs over $25 billion annually. Current pharmacological therapies may be expensive, cause serious adverse effects, and fail to effectively improve pain and function. Finding new and effective non-pharmacological treatments for FM patients is urgently needed.

We propose to conduct the first comparative effectiveness trial of Tai Chi vs. aerobic exercise (a recommended component of the current standard of care) and to evaluate effectiveness under different Tai Chi dosing schedules in a large FM population. We aim to (1) demonstrate that, compared to aerobic exercise, Tai Chi is a more effective intervention for managing the pain and improving the functional limitations that impact quality of life for FM patients, and 2) determine the optimal frequency and duration of a supervised Tai Chi intervention in relation to short and long-term effectiveness. To achieve this goal, we will conduct a single-blind, randomized controlled trial of Tai Chi vs. aerobic exercise in 216 patients who meet the American College of Rheumatology criteria for FM. Patients will be randomized to one of four Tai Chi intervention groups: 12 or 24 weeks of supervised Tai Chi given once or twice per week, or a supervised aerobic exercise control: 2x/week for 24 weeks. All groups will have a 52-week follow-up. The primary outcome will be the FM Impact Questionnaire total score at 24 weeks. Secondary outcomes include the measures of widespread pain, functional performance, psychological functioning, self-efficacy, sleep quality, and quality of life at 12, 24, and 52 weeks.

Successful completion of the proposed study will determine the ideal regimen of Tai Chi and demonstrate that Tai Chi can be a simple, effective, and durable treatment for this therapeutically challenging disorder.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 21 years or older.
  • Fulfills the American College of Rheumatology (ACR) 1990 classification criteria for FM: (1) a history of widespread musculoskeletal pain on the right and left sides of the body as well as above and below the waist for a minimum duration of 3 months, and (2) pain in 11 or more of 18 specific tender points with moderate or greater tenderness reported upon digital palpation.27
  • Fulfills the ACR 2010 diagnostic criteria for FM: (WPI ≥7 AND SS ≥5) OR (WPI 3-6 AND SS ≥9) and does not have a disorder that would otherwise explain the pain28
  • Willing to complete the 12-week or 24-week study, including once or twice-a-week exercise sessions.
  • Willing to abstain from Tai Chi or other new formalized exercise programs until completion of the study if randomized to the Aerobic Exercise.
  • Willing to abstain from Aerobic Exercise or other new formalized exercise programs until completion of the study if randomized to Tai Chi

Exclusion criteria

  • Prior experience with Tai Chi or other similar types of Complementary and Alternative Medicine in the past 1 year such as Qi gong and yoga since these share some of the principles of Tai Chi.
  • Dementia, neurological disease, cancer, cardiovascular disease, pulmonary disease, metabolic disease, renal disease, liver disease, or other serious medical conditions limiting ability to participate in the Tai Chi or Aerobic Exercise programs, as determined by the study physicians.
  • Any other diagnosed medical condition known to contribute to FM symptomatology that is not under adequate control for the study period such as thyroid disease, inflammatory arthritis, systemic lupus erythematosus, rheumatoid arthritis, myositis, vasculitis or Sjogren's syndrome.
  • Inability to pass the Mini-Mental Status examination (with a score below 24) 29
  • Enrollment in any other clinical trial within the last 30 days
  • Plan to permanently relocate from the region during the trial period
  • Positive urine pregnancy test at baseline or planning pregnancy within the study period
  • Not English-Speaking: English is the only language to be used during the exercise training program. Our self-reported outcome measures are obtained from validated English-version questionnaires. In addition, using other languages would likely require separate classes, recruitment and instructors which are beyond our current study scope

Treatment and study plan

Lower frequency, shorter period of Tai Chi

Behavioral

12 weeks of supervised Tai Chi classes, 1x/week

Higher frequency, shorter period of Tai Chi

Behavioral

12 weeks of supervised Tai Chi classes, 2x/week

Shorter frequency, longer period of Tai Chi

Behavioral

24 weeks of supervised Tai Chi classes, 1x/week

Higher frequency, longer period of Tai Chi

Behavioral

24 weeks of supervised Tai Chi classes, 2x/week

Aerobic Exercise Training

Behavioral

24 weeks of supervised aerobic exercise training, 2x/week

Primary outcomes

  1. Change in Fibromyalgia Impact Questionnaire (FIQ) from baseline to 24 weeks

    Time frame: Week 0, Week 24

    Overall severity of FM, intensity of pain, physical function, fatigue, morning tiredness, depression, anxiety, job difficulty, and overall well-being

Secondary outcomes

  1. Change in Fibromyalgia Impact Questionnaire at follow-up

    Time frame: Week 0, Week 12, Week 52

    Overall severity of FM, intensity of pain, physical function, fatigue, morning tiredness, depression, anxiety, job difficulty, and overall well-being

  2. FM Symptom Severity Scale

    Time frame: Week 0, Week 12, Week 24, Week 52

    FM symptoms

  3. Body Mass Index (BMI)

    Time frame: Week 0, Week 12, Week 24, Week 52

    General health

  4. Medical Outcome Study Short Form 36 (SF-36)

    Time frame: Week 0, Week 12, Week 24, Week 52

    General health/functional status

  5. Patient Global Assessment

    Time frame: Week 0, Week 12, Week 24, Week 52

    General health/functional status

  6. The Beck Depression Inventory II

    Time frame: Week 0, Week 12, Week 24, Week 52

    Depression

  7. The Chronic Pain Self-Efficacy Scale (CPSS)

    Time frame: Week 0, Week 12, Week 24, Week 52

    Chronic pain

  8. The Pittsburg Sleep Quality Index (PSQI)

    Time frame: Week 0, Week 12, Week 24, Week 52

    Sleep quality

  9. The Sleep Quality Numeric Rating Scale (NRS)

    Time frame: Week 0, Week 12, Week 24, Week 52

    Sleep quality

  10. 6-Minute Walk

    Time frame: Week 0, Week 12, Week 24, Week 52

    Walking ability and Endurance

  11. The Chair Stand Test

    Time frame: Week 0, Week 12, Week 24, Week 52

    Physical functioning

  12. The brief Outcome Expectation Scale (OES)

    Time frame: Week 0, Week 12, Week 24, Week 52

    Outcome expectations

  13. Health Assessment Questionnaire (HAQ)

    Time frame: Week 0, Week 12, Week 24, Week 52

    Healthcare cost and utilization

  14. PROMIS Health Assessment Questionnaire (HAQ)

    Time frame: Week 0, Week 12, Week 24, Week 52

    Health status

  15. Muscle Strength/Power and Balance

    Time frame: Week 0, Week 12, Week 24, Week 52

    Physical functioning as assessed by muscle strength and power, and balance

  16. CHAMPS Activities Questionnaire for Older Adults

    Time frame: Week 0, Week 12, Week 24, Week 52

    Activity levels

Sponsors and collaborators

Lead sponsor

Tufts Medical Center

Other

Collaborators

  • National Center for Complementary and Integrative Health (NCCIH)

Registry information

Official study title

Tai Chi and Aerobic Exercise for Fibromyalgia

Acronym: FMEx

Important dates

Study start
2012
Primary completion
2015
Study completion
2015
First posted
Aug 19, 2011
Registry last updated
Feb 10, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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