Treating Chronic Pain in Gulf War Illness
Primary Purpose
Chronic Pain, Gulf War Illness, Chronic Illness
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Yoga Group
Pain Management Wellness Group
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Pain focused on measuring Chronic Pain, Veterans, Gulf War Illness
Eligibility Criteria
Inclusion Criteria:
- Served in the military in 1990-1991, regardless of deployment.
- History of chronic pain.
- Able to attend weekly visits at the study center for 10 weeks.
- If on a psychotropic medication, the regimen will be stable for at least 4 weeks, prior to entry in the study.
Exclusion Criteria:
- Participation in another clinical trial.
- Unable to visit the study center.
- Unable to stand or walk.
Sites / Locations
- VA Palo Alto Health Care System
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Yoga Group
Pain Management Wellness Group
Arm Description
Postures, meditation, breathing exercises
Behavioral medicine
Outcomes
Primary Outcome Measures
Pain (Brief Pain Inventory - Short Form) - Pain Severity
Model - estimated change in the Pain Severity subscale of the Brief Pain Inventory - Short Form from baseline to end of treatment. The subscale's minimum score is 0; maximum is 10; more negative change scores indicate greater improvement from baseline to end of treatment
Pain (Brief Pain Inventory - Short Form) - Pain Interference
Model - estimated change in the Pain Interference subscale of the Brief Pain Inventory - Short Form from baseline to end of treatment. The subscale's minimum score is 0; maximum is 10; more negative change scores indicate greater improvement from baseline to end of treatment.
Secondary Outcome Measures
Fatigue (6-Minute Walk Test)
Increase from baseline to end of treatment in distance walked during 6-Minute Walk Test. Greater values indicate more increase and therefore a more positive outcome.
Change in Number of Participants Who Used Analgesic Medication
Change in number of participants who self-reported use of analgesic medication(s) from Week 0 to Week 10.
Change in Number of Participants Who Used Nonsteroidal Anti-inflammatory Drugs
Change in number of participants who self-reported use of Nonsteroidal Anti-inflammatory Drug(s) from Week 0 to Week 10.
Change in Number of Participants Who Used Opiate Medication
Change in number of participants who self-reported use of Opiate Medication(s) from Week 0 to Week 10.
Full Information
NCT ID
NCT02378025
First Posted
February 26, 2015
Last Updated
May 29, 2020
Sponsor
Palo Alto Veterans Institute for Research
Collaborators
United States Department of Defense
1. Study Identification
Unique Protocol Identification Number
NCT02378025
Brief Title
Treating Chronic Pain in Gulf War Illness
Official Title
A Multimodal Evaluation of the Comparative Efficacy of Yoga Versus a Patient Centered Support Group for Treating Chronic Pain in Gulf War Illness
Study Type
Interventional
2. Study Status
Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
June 1, 2015 (Actual)
Primary Completion Date
March 2018 (Actual)
Study Completion Date
March 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Palo Alto Veterans Institute for Research
Collaborators
United States Department of Defense
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to determine whether yoga is effective for the treatment of chronic pain in Gulf War Illness.
Detailed Description
Background:
Many military personnel who participated in the Gulf War in 1990-1991 reported negative health consequences subsequent to their deployment. The most prevalent of these health consequences involves a triad of symptoms that include fatigue, pain and cognitive disturbances, commonly referred to as "Gulf War Illness" (GWI). No clear, unifying patho-physiological disease process or effective treatment has yet been identified for GWI. Results from a diverse spectrum of research studies support the view that veterans with GWI are medically ill, but the physiological abnormalities that contribute to their illness are not currently well understood nor sufficiently treated by conventional medicine. While the cause of GWI remains unknown, a potential link between GWI and autonomic nervous system (ANS) dysregulation has been suggested.
Yoga has been suggested to exert its therapeutic effects through adjusting imbalances in the ANS. In addition, yoga has been shown to be clinically effective in treating many of the physical symptoms typically found in GWI, including chronic pain and fatigue. As chronic pain is perhaps the most prevalent and debilitating symptom of GWI, we propose to target pain. Significantly for this application, no improvements in pain have yet been reported in any clinical trial involving GWI. Furthermore, no published studies have investigated yoga as an intervention in GWI.
Objectives:
The primary objective is to investigate yoga for the treatment of chronic pain in veterans with GWI. A secondary objective is to provide veterans with skills in yoga breathing, postures, and meditation that can be used to promote health and well-being.
Hypothesis 1 (primary):
The subjective experience of pain, as measured by the Brief Pain Inventory-Short Form, will be reduced at end of treatment in the group given a 10-week yoga treatment program, compared to a pain support group (control).
This effect will be sustained across time and will be found at the end of the 24-week post-treatment follow-up.
Hypothesis 2 (secondary):
Yoga will have a beneficial effect on general well-being; thus, compared to the control group, the yoga treatment group will show benefits across a broad range of measures, including quality of life, fatigue, and medication use.
Specific Aims:
To assess the efficacy of yoga in reducing chronic pain and determine if the health-related benefits of yoga persist after termination of the treatment program.
To obtain symptom-based outcome measures for veterans with GWI (before and after randomization) to assess pain, fatigue, physical functional status and quality of life.
Study Design:
The intervention to be tested is a 10-week yoga treatment program that has been specially designed for the treatment of chronic pain, as experienced by veterans with GWI. One hundred patients will be randomly assigned to one of two treatment groups: group yoga or a pain management wellness group (control). The control group has been carefully designed to control for many features of a yoga intervention. Patients in both groups will attend weekly classes for 10 weeks, followed by 6 months of follow up. Monitoring will include periodic measures of pain, fatigue, quality of life, and ANS function.
Impact:
Despite increasing demand from veterans for yoga and other forms of complementary and alternative treatments, the provision of yoga in veteran healthcare remains sparse. This is due, in large part, to a lack of randomized clinical trials capable of demonstrating the efficacy and safety of yoga for the treatment of conditions such as GWI. Such a demonstration would strengthen the case to offer yoga as a widely-available treatment for pain in GWI and would help promote yoga as part of integrative healthcare. This treatment trial is designed to begin to determine potential mechanisms of pain maintenance in GWI. If yoga leads to improvement in pain outcome, this would support performing a larger clinical trial of yoga for treating pain and other symptoms of GWI.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Pain, Gulf War Illness, Chronic Illness
Keywords
Chronic Pain, Veterans, Gulf War Illness
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
75 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Yoga Group
Arm Type
Experimental
Arm Description
Postures, meditation, breathing exercises
Arm Title
Pain Management Wellness Group
Arm Type
Active Comparator
Arm Description
Behavioral medicine
Intervention Type
Behavioral
Intervention Name(s)
Yoga Group
Intervention Description
A 10-week yoga course designed to treat pain.
Intervention Type
Behavioral
Intervention Name(s)
Pain Management Wellness Group
Intervention Description
A 10-week behavioral therapy course designed to treat pain.
Primary Outcome Measure Information:
Title
Pain (Brief Pain Inventory - Short Form) - Pain Severity
Description
Model - estimated change in the Pain Severity subscale of the Brief Pain Inventory - Short Form from baseline to end of treatment. The subscale's minimum score is 0; maximum is 10; more negative change scores indicate greater improvement from baseline to end of treatment
Time Frame
Week 10 minus Week 0
Title
Pain (Brief Pain Inventory - Short Form) - Pain Interference
Description
Model - estimated change in the Pain Interference subscale of the Brief Pain Inventory - Short Form from baseline to end of treatment. The subscale's minimum score is 0; maximum is 10; more negative change scores indicate greater improvement from baseline to end of treatment.
Time Frame
Week 10 minus Week 0
Secondary Outcome Measure Information:
Title
Fatigue (6-Minute Walk Test)
Description
Increase from baseline to end of treatment in distance walked during 6-Minute Walk Test. Greater values indicate more increase and therefore a more positive outcome.
Time Frame
Week 0, Week 10
Title
Change in Number of Participants Who Used Analgesic Medication
Description
Change in number of participants who self-reported use of analgesic medication(s) from Week 0 to Week 10.
Time Frame
Week 0, Week 10
Title
Change in Number of Participants Who Used Nonsteroidal Anti-inflammatory Drugs
Description
Change in number of participants who self-reported use of Nonsteroidal Anti-inflammatory Drug(s) from Week 0 to Week 10.
Time Frame
Week 0, Week 10
Title
Change in Number of Participants Who Used Opiate Medication
Description
Change in number of participants who self-reported use of Opiate Medication(s) from Week 0 to Week 10.
Time Frame
Week 0, Week 10
10. Eligibility
Sex
All
Minimum Age & Unit of Time
42 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Served in the military in 1990-1991, regardless of deployment.
History of chronic pain.
Able to attend weekly visits at the study center for 10 weeks.
If on a psychotropic medication, the regimen will be stable for at least 4 weeks, prior to entry in the study.
Exclusion Criteria:
Participation in another clinical trial.
Unable to visit the study center.
Unable to stand or walk.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Bayley, PhD
Organizational Affiliation
VA Palo Alto Heath Care System
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Palo Alto Health Care System
City
Palo Alto
State/Province
California
ZIP/Postal Code
94304
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
33984356
Citation
Mathersul DC, Dixit K, Avery TJ, Schulz-Heik RJ, Zeitzer JM, Mahoney LA, Cho RH, Bayley PJ. Heart rate and heart rate variability as outcomes and longitudinal moderators of treatment for pain across follow-up in Veterans with Gulf War illness. Life Sci. 2021 Jul 15;277:119604. doi: 10.1016/j.lfs.2021.119604. Epub 2021 May 11.
Results Reference
derived
PubMed Identifier
33218747
Citation
Bayley PJ, Schulz-Heik RJ, Cho R, Mathersul D, Collery L, Shankar K, Ashford JW, Jennings JS, Tang J, Wong MS, Avery TJ, Stanton MV, Meyer H, Friedman M, Kim S, Jo B, Younger J, Mathews B, Majmundar M, Mahoney L. Yoga is effective in treating symptoms of Gulf War illness: A randomized clinical trial. J Psychiatr Res. 2021 Nov;143:563-571. doi: 10.1016/j.jpsychires.2020.11.024. Epub 2020 Nov 11.
Results Reference
derived
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Treating Chronic Pain in Gulf War Illness
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