Cognitive-Behavioral Therapy and Tai Chi Chih for Patients With Rheumatoid Arthritis

University of California, Los Angeles (UCLA)

Status: Completed

Conditions: Rheumatoid Arthritis

Treatments: Behavioral: Health Education Seminar; Behavioral: Cognitive Behavioral Therapy; Behavioral: Tai Chi Chih

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT00072657

R01AR049840 (U.S. NIH Grant/Contract)

NIAMS-095

Details and patient eligibility

About

Rheumatoid arthritis (RA) is a chronic illness. Patients with RA often experience significant pain and depression. This study will evaluate two programs designed to improve the symptoms of RA: cognitive-behavioral therapy (CBT) and Tai Chi Chih (TCC), compared to a health education seminar.

Full description

Rheumatoid arthritis is a progressive inflammatory illness marked by severe functional declines, significant economic and social costs, and significant psychological distress. Environmental and psychosocial factors such as stress, mood disturbance, and coping mechanisms may contribute to changes in important health outcomes, including disability and disease activity in RA. This study will compare CBT with TCC, a relaxation-based intervention, combining elements of slow gentle movement with meditation, against a more traditional health education seminar. Outcome measures will include psychological adaptation, mood disturbance, sleep quality, physiological adaptation, and disease severity.

Two hundred-ten patients will be randomly assigned to either CBT, TCC, or a control group. The CBT intervention will have three phases: 1) education on the nature of the adjustment process in chronic illness, 2) coping skill development, and 3) generalization and application of skills to everyday situations. Participants in the CBT group will attend 12 weekly group sessions of about 2 hours each. Participants in the TCC group will learn to perform 18 movements under the guidance of an expert TCC teacher. TCC participants will have 50 to 60 minute biweekly sessions during the 12-week study. Control group participants will attend weekly group educational sessions; these sessions will provide general knowledge about arthritis health and illness, and will include lectures, demonstrations, and question-and-answer sessions with experts in rheumatology, sleep science, and behavioral medicine.

Participants will be assessed prior to beginning treatment, at mid-treatment (Week 6) and again at the end of treatment (Week 12 to 13). The long term effect of interventions will be assessed at follow-up interviews 4 months and 8 months after the end of formal treatment. Psychosocial adaptation, mood disturbance and sleep quality, self-reported pain, and immune function will be measured at all five assessment periods.

Enrollment: 106 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Diagnosis of RA as defined by the American College of Rheumatology (ACR) and consistent with revised criteria for RA
• Stable disease-modifying drug regimen for 3 months prior to study entry, with no change in drug dosage for at least 3 months prior to study entry
• Relatively stable disease course for 3 months prior to study entry
• If treated with corticosteroids, must be on a stable dosage for 3 months prior to study entry
• If taking prednisone, must be on a dosage less than or equal to 10 mg/day or equivalent
• Resides in Greater Los Angeles area

Exclusion criteria

• Inactive RA conditions defined as "in remission"
• Experiencing frequent, severe disease flares that require changes in primary disease-modifying regimen
• Serious medical conditions, including: diabetes, congestive heart failure, renal failure requiring specific treatment, cancer (unless cured for period of 5 years or more), unregulated endocrine disorders (including thyroid disorders), chronic uncontrolled infection, or any uncontrolled medical condition that may interfere with the study
• Use of analgesics (e.g., opioids) other than acetaminophen or non-steroidal anti-inflammatory agents prescribed for RA treatment, tramadol (Ultram) or Tylenol with codeine on an as-needed basis, or propoxyphen (Darvocet, Wygesic)
• Use of oxycodone (Percocet), hydrocodone (Vicodin), morphine, or hydromorphone (Dilaudid)
• Use of high levels of methotrexate (greater than 7.5 mg)
• Use of nitrogen mustard, cyclosporine, monoclonal antibodies, or cyclophosphamide within the 6 months prior to study entry
• Serious psychiatric conditions, such as bipolar disorder, psychotic disorders, or organic brain syndromes
• At risk for suicide
• Dependent on canes, walkers, or other assistive devices
• Unable to commit to study schedule/itinerary or unwilling to be assigned to any of the 3 treatment groups

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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106 participants in 3 patient groups

1

Experimental group

Description:

Participants will partake in cognitive behavioral therapy for 12 weeks.

Treatment:

Behavioral: Cognitive Behavioral Therapy

2

Experimental group

Description:

Participants will partake in tai chi chih for 12 weeks.

Treatment:

Behavioral: Tai Chi Chih

3

Active Comparator group

Description:

Participants will act as a control and attend educational sessions for 12 weeks.

Treatment:

Behavioral: Health Education Seminar