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Relaxation Response Training for the Treatment of Rheumatoid Arthritis

Primary Purpose

Rheumatoid Arthritis

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Relaxation response and cognitive behavioral therapy
Relaxation response
RA education
Sponsored by
Brigham and Women's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rheumatoid Arthritis focused on measuring Treatment, Pain, Relaxation Response, Cognitive Behavioral Therapy

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria RA as defined by the American College of Rheumatology English literacy and fluency Exclusion criteria Major medical condition or illness which limits life expectancy or results in severe symptoms or functional disability (Duke Severity of Illness score > 0.85) Fibromyalgia Received or currently receiving psychosocial treatment for RA Unavailability for Month 12 follow-up

Sites / Locations

  • Brigham & Women's Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

CBT plus relaxation response

Relaxation Response

Education

Arm Description

Participants will receive cognitive behavioral therapy plus relaxation response training

Participants will receive relaxation response training

Participants will receive rheumatoid arthritis education

Outcomes

Primary Outcome Measures

Somatic symptoms as assessed by the Rheumatoid Arthritis Symptom Questionnaire

Secondary Outcome Measures

Role impairment and functional status as assessed with the Functional Status Questionnaire
Medical care utilization as assessed with the hospital's automated encounter database

Full Information

First Posted
March 20, 2003
Last Updated
January 15, 2014
Sponsor
Brigham and Women's Hospital
Collaborators
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
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1. Study Identification

Unique Protocol Identification Number
NCT00056667
Brief Title
Relaxation Response Training for the Treatment of Rheumatoid Arthritis
Official Title
Relaxation Response, Somatic Style and Rheumatoid Arthritis
Study Type
Interventional

2. Study Status

Record Verification Date
January 2014
Overall Recruitment Status
Completed
Study Start Date
July 2001 (undefined)
Primary Completion Date
December 2006 (Actual)
Study Completion Date
December 2006 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brigham and Women's Hospital
Collaborators
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will evaluate the relative effectiveness of Relaxation Response (RR) training for the treatment of rheumatoid arthritis (RA). The study will compare RR training to RR training with cognitive behavioral therapy and to a standard RA education program.
Detailed Description
RR training is a part of most multi-component psychosocial therapies for RA. RR training may decrease perceived psychosocial stress and autonomic tone, which in turn diminishes pain and the anticipatory anxiety associated with pain. RR training involves learning relaxation techniques which include diaphragmatic breathing, progressive skeletal muscle relaxation, and the induction of a state of focused attention on a chosen word, phrase, or image. In clinical practice, RR training is generally administered as one component of RA therapy. In this study, the effectiveness of RR training will be evaluated when RR training is administered alone and in combination with a cognitive behavioral therapy program. The cognitive behavior techniques include problem solving, relabeling, enhanced awareness of pain behaviors, and attention refocusing. The effectiveness of RR training will be evaluated in comparison to standard RA education that includes topics such as the nature of RA disease, medical therapies, physical activities, nutrition, and pain mechanisms. After a baseline assessment of health beliefs, RA severity, social support, and psychological distress, patients will be randomized to one of three study arms. Patients in Arm A will complete six individualized weekly RR training sessions. Patients will receive a 20-minute audiotape to guide them through the exercise; they are asked to practice 5 to 7 times per week. Patients in Arm B will learn cognitive behavioral and RR techniques during eight weekly sessions. Patients in Arm C will receive standard RA education. After the initial training, all patients will be followed up with monthly telephone conversations for 4 months. Patients will have follow-up study visits at Months 6 and 12. Follow-up study visits include a medical interview, physical exam, and blood tests.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rheumatoid Arthritis
Keywords
Treatment, Pain, Relaxation Response, Cognitive Behavioral Therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
168 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CBT plus relaxation response
Arm Type
Experimental
Arm Description
Participants will receive cognitive behavioral therapy plus relaxation response training
Arm Title
Relaxation Response
Arm Type
Active Comparator
Arm Description
Participants will receive relaxation response training
Arm Title
Education
Arm Type
Placebo Comparator
Arm Description
Participants will receive rheumatoid arthritis education
Intervention Type
Behavioral
Intervention Name(s)
Relaxation response and cognitive behavioral therapy
Other Intervention Name(s)
RRCBT
Intervention Description
The cognitive behavioral therapy program wwill incorporate relaxation training, a modified version of the RA treatment program developed by Bradley et al (1987) and shown to be effective. The cognitive behavioral techniques include problem solving, relabeling, enhanced awareness of pain behaviors, and attention refocusing. The RR component includes instruction in diaphragmatic breathing along with progressive skeletal muscle relaxation. The intervention will be modified from the original program in that neither biofeedback training nor participation of family members will be included. Consequently, the number of weekly group sessions will be reduced from 14 to 12. Homework will be given at the end of each session, to be completed and brought in for review to the next session.
Intervention Type
Behavioral
Intervention Name(s)
Relaxation response
Other Intervention Name(s)
RR
Intervention Description
The relaxation response (RR) consists of a set of integrated physiological changes elicited when a participant engages in the repetitive mental action of focusing on a word, phrase, or image, while passively ignoring distracting thoughts. These changes include decreased oxygen consumption, heart rate, arterial blood pressure, respiratory rate, and arterial blood lactate, along with slight increases in skeletal muscle blood flow. The long-term physiologic changes of participants eliciting the relaxation response are consistent with reduced norepinephrine end organ responsivity. These latter changes provide a plausible psychophysiological mechanism for longer-term actions of the RR.
Intervention Type
Other
Intervention Name(s)
RA education
Intervention Description
RA education programs have been widely used to supplement routine medical care. They have been found to be of modest benefit, particularly in terms of knowledge about the condition and its treatment. The long-term effects on pain and level of function are less. When used as an attention control, such educational programs have been found to be as credible and as well attended as the active experimental treatment (Professor Francis Keefe, Personal Communication). In this study, patients randomized to the control condition will receive 8 weekly sessions of RA education, in groups of 6-10 patients each, using portions of the Arthritis Self-Management Program and incorporating printed and videotaped materials available from the Arthritis Foundation.
Primary Outcome Measure Information:
Title
Somatic symptoms as assessed by the Rheumatoid Arthritis Symptom Questionnaire
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Role impairment and functional status as assessed with the Functional Status Questionnaire
Time Frame
12 months
Title
Medical care utilization as assessed with the hospital's automated encounter database
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria RA as defined by the American College of Rheumatology English literacy and fluency Exclusion criteria Major medical condition or illness which limits life expectancy or results in severe symptoms or functional disability (Duke Severity of Illness score > 0.85) Fibromyalgia Received or currently receiving psychosocial treatment for RA Unavailability for Month 12 follow-up
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arthur J. Barsky, MD
Organizational Affiliation
Brigham & Women's Hospital, Boston, MA
Official's Role
Principal Investigator
Facility Information:
Facility Name
Brigham & Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
20621334
Citation
Barsky AJ, Ahern DK, Orav EJ, Nestoriuc Y, Liang MH, Berman IT, Kingsbury JR, Sy JT, Wilk KG. A randomized trial of three psychosocial treatments for the symptoms of rheumatoid arthritis. Semin Arthritis Rheum. 2010 Dec;40(3):222-32. doi: 10.1016/j.semarthrit.2010.04.001.
Results Reference
derived

Learn more about this trial

Relaxation Response Training for the Treatment of Rheumatoid Arthritis

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