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Comparing Tai Chi Chih and Relaxation Therapy in the Treatment of Rheumatoid Arthritis - Article


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Relaxation

 




Clinical Trial: Comparing Tai Chi Chih and Relaxation Therapy in the Treatment of Rheumatoid Arthritis

This study is currently recruiting patients.

Sponsored by: National Center for Complementary and Alternative Medicine (NCCAM)
Information provided by: National Center for Complementary and Alternative Medicine (NCCAM)

Purpose

The purpose of this study is to compare the effectiveness of relaxation therapy and tai chi in treating the symptoms of rheumatoid arthritis (RA).

Condition Treatment or Intervention Phase
Arthritis, Rheumatoid
 Behavior: Tai Chi Chih
 Behavior: Relaxation training
Phase II
Phase III

MedlinePlus related topics:  Rheumatoid Arthritis

Study Type: Interventional
Study Design: Treatment, Randomized, Single Blind, Efficacy Study

Official Title: Efficacy of CAM Interventions in Rheumatoid Arthritis

Further Study Details: 
Primary Outcomes: RA-related disability; Health functioning
Expected Total Enrollment:  100

Study start: November 2004;  Expected completion: November 2007
Last follow-up: January 2007;  Data entry closure: March 2007

RA is a debilitating disease characterized by inflammation of the joints, leading to chronic pain, loss of function, and disability. Complementary and alternative medicine (CAM) treatments are being used with increased frequency by patients with chronic pain and rheumatic diseases to relieve their symptoms. While patients find these treatments helpful, there is limited scientific evidence of the effectiveness of these interventions. This study will compare relaxation therapy (a commonly used treatment for RA) to tai chi chih (a combination of slow, deliberate movements and meditation) in treating the symptoms of RA.

Participants will be randomly assigned to receive 12 weeks of either relaxation therapy or tai chi chih. At study entry and Weeks 6 and 12, participants will complete questionnaires about their RA symptoms, health functioning, overall quality of life, and complete a brief medical exam.

Eligibility

Ages Eligible for Study:  18 Years   -   85 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

  • Active adult onset rheumatoid arthritis
  • Stable on disease-modifying antirheumatic drugs (DMARDs) or biologic medications
  • Able to walk without use of an assistive device
  • Resides in greater Los Angeles area
  • Willing and able to comply with study requirements

Exclusion Criteria:

  • Uncontrolled or untreated medical conditions
  • Frequent or uncontrolled disease flares
  • Use of certain medications any medical condition deemed by the investigators to interfere with either the patient's safe participation or interpretation of the study data

Location and Contact Information

Jennifer Pike, PhD      310-206-3257    jpike@ucla.edu

California
      University of California, Los Angeles Medical Center, Los Angeles,  California,  90095,  United States; Recruiting
Jennifer Pike, PhD  310-206-3257    jpike@ucla.edu 
Jennifer Pike, PhD,  Principal Investigator

      Cedars-Sinai Medical Center, Los Angeles,  California,  90048,  United States; Recruiting

Study chairs or principal investigators

Jennifer Pike, PhD,  Principal Investigator,  University of California, Los Angeles   

More Information

Study ID Numbers:  AT002307-01
Record last reviewed:  March 2005
Last Updated:  March 24, 2005
Record first received:  November 15, 2004
ClinicalTrials.gov Identifier:  NCT00096759
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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November 25, 2009



Page Updated: January 17, 2009
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