Cognitive-Behavioral Therapy and Tai Chi Chih for Patients With Rheumatoid Arthritis
CompletedNot applicableNCT00072657
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
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.
Study details
- Official title
- Behavioral Treatments for Rheumatoid Arthritis
- Conditions
- Interventions
- Behavioral: Cognitive Behavioral Therapy
- Behavioral: Tai Chi Chih
- Behavioral: Health Education Seminar
- Sponsor
- University of California, Los Angeles
- Collaborators
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
- Start date
- 2004-02
- Primary completion
- 2009-03
- Sex
- All
- Age range
- from 18 Years
- Results posted
- No results posted in this snapshot
- Countries
- United States
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
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
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT00072657