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Overcoming Pain Through Yoga in the Military (OPTYM)

Primary Purpose

Chronic Low Back Pain, Chronic Neck Pain

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Yoga: Active Hatha
Yoga: Restorative
Sponsored by
University of California, San Diego
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Chronic Low Back Pain focused on measuring Chronic Low Back Pain, CLBP, Chronic Neck Pain, CNP, Chronic Pain, Military, Active Duty, Yoga, Mindbody

Eligibility Criteria

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

Inclusion Criteria:

  • Diagnosis of CLBP or CNP > 6 months
  • Willing to attend a yoga program for 12 weeks
  • Willing to complete 3 assessments
  • English literacy
  • Have had no changes in pain treatments in the past month
  • Willing to not change pain treatments during study unless medically necessary
  • Have not practiced yoga more than 2x in the last 12 months

Exclusion Criteria:

  • Back or neck surgery within the last year
  • Back or neck pain due to specific systemic problem (e.g., lupus, scoliosis)
  • Severe vertebral disk problems,
  • Persistent sciatica or nerve compression > 3 months
  • Coexisting chronic pain problem (e.g., migraine headaches, fibromyalgia)
  • Serious or unstable psychiatric illness (e.g., psychosis, mania, episode, or substance dependence)
  • Major coexisting medical illness (e.g., cancer, COPD, morbid obesity)
  • Positive Romberg test (with or without sensory neuropathy)

Sites / Locations

  • UCSD's Health Services Research Center
  • Navy Medical Center San Diego

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Hatha Yoga

Restorative Yoga

Arm Description

This arm will receive the active Hatha yoga intervention. Instructors lead participants through various yoga poses for 60-minutes, 1-2x weekly for 12 weeks, and daily home practice is recommended.

This arm will receive a restorative yoga intervention. Instructors guide participants through relaxation exercises, typically with eyes closed, laying down, and minimal movement 60-minutes, 1-2x weekly for 12 weeks.

Outcomes

Primary Outcome Measures

Pain Interference
Brief Pain Inventory (BPI) : Self-Report measure of pain interference and pain severity consisting of 14 items. The measure includes front and back body diagrams to describe areas of pain, four pain severity items and seven pain interference items rated on 0-10 scales, and one question about percentage of pain relief by analgesics. The pain interference score is the mean of the 7 interference items. The pain severity score is the mean of 4 severity items. Scale scores are the mean of relevant items. Thus, scores range from 0-10 with higher scores indicating more pain interference.

Secondary Outcome Measures

Roland-Morris Disability Questionnaire
Self-report measure consisting of 23 questions that ask about limitations experienced for a variety of daily activities. Scale scores are the sum of items endorsed, thus scores range from 0-23 with higher scores indicating more back pain-related disability.
BPI Pain Severity
Brief Pain Inventory (BPI) : Self-Report measure of pain severity consisting of 4 items. The measure includes front and back body diagrams to describe areas of pain, four pain severity items and seven pain interference items rated on 0-10 scales, and one question about percentage of pain relief by analgesics. The pain severity score is the mean of 4 severity items. Scale scores are the mean of relevant items. Thus, scores range from 0-10 with higher scores indicating greater pain severity.
Neck Disability Index
Ten-item self-report measure to assess neck pain interference in daily life activities. Each of the 10 items is scored from 0 - 5. The items are summed and scores range from 0-50 with higher scores indicating greater disability due to neck pain.

Full Information

First Posted
March 2, 2018
Last Updated
February 15, 2023
Sponsor
University of California, San Diego
Collaborators
United States Naval Medical Center, San Diego, National Center for Complementary and Integrative Health (NCCIH)
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1. Study Identification

Unique Protocol Identification Number
NCT03504085
Brief Title
Overcoming Pain Through Yoga in the Military
Acronym
OPTYM
Official Title
Mind/Body Interventions for Chronic Low Back and Neck Pain in Military Personnel
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
May 1, 2018 (Actual)
Primary Completion Date
May 31, 2020 (Actual)
Study Completion Date
May 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, San Diego
Collaborators
United States Naval Medical Center, San Diego, National Center for Complementary and Integrative Health (NCCIH)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Our primary aim is to assess the feasibility of conducting yoga research among active-duty military personnel with Chronic Low Back Pain (CLBP) and/or Chronic Neck Pain (CNP). In addition, we will evaluate the yoga intervention preferences and refine an existing yoga intervention to address those needs. The study will prepare us for a R01 funded pragmatic clinical trial of yoga for CLBP and CNP in active-duty military.
Detailed Description
In preparation for a full-scale study via a subsequent R01 proposal, our study objective is to examine the feasibility and acceptability of conducting a yoga RCT among active-duty military personnel with CLBP/CNP in military and community settings. The study will be conducted in two phases: Phase 1 (completed) involved obtaining IRB approval to conduct research in military settings, collecting qualitative data from stakeholders on attitudes and preferences for yoga interventions, and refining the existing Yoga for CLBP intervention for the needs of active-duty military and persons with CNP. Phase 2 will recruit and randomize 50 military personnel with CLBP or CNP to either active hatha or restorative yoga. Pain interference, pain severity, physical function, opioid medication use, and mental health outcomes are of primary interest. Mechanisms will also be studied. The specific aims are as follows: Aim 1: Evaluate and navigate barriers and facilitators for obtaining IRB approval to conduct randomized controlled intervention studies with active-duty military personnel. Aim 2: Evaluate the acceptability of and preferences for yoga interventions among active-duty military personnel with CLBP/CNP. Aim 3: Refine and modify the existing Yoga for CLBP intervention to address CNP, and the needs of active-duty military personnel. Aim 4: Evaluate the feasibility of recruitment of active-duty military personnel with CLBP/CNP into a yoga RCT. Aim 5: Evaluate the adherence of this population to the two yoga interventions. Aim 6: Obtain effect size estimates to inform power analyses for a full-scale RCT. Accomplishing these aims will prepare us for an R01 proposal to study the efficacy of yoga for military personnel with CLBP/CNP in a full-scale randomized, controlled trial. To be successful and maximize the scientific knowledge obtained from an R01 study, it is crucial to first establish working relationships with military researchers, ensure that recruitment and randomized assignment are feasible, pilot test measurement strategies, and ensure that both interventions will be well-attended and have been optimally chosen.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Low Back Pain, Chronic Neck Pain
Keywords
Chronic Low Back Pain, CLBP, Chronic Neck Pain, CNP, Chronic Pain, Military, Active Duty, Yoga, Mindbody

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
We will be conducting a pilot RCT with two types of yoga interventions. A total of 50 participants will be randomized to attend either active Hatha yoga or restorative yoga. Enrollment will be conducted on a rolling basis.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
49 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Hatha Yoga
Arm Type
Experimental
Arm Description
This arm will receive the active Hatha yoga intervention. Instructors lead participants through various yoga poses for 60-minutes, 1-2x weekly for 12 weeks, and daily home practice is recommended.
Arm Title
Restorative Yoga
Arm Type
Active Comparator
Arm Description
This arm will receive a restorative yoga intervention. Instructors guide participants through relaxation exercises, typically with eyes closed, laying down, and minimal movement 60-minutes, 1-2x weekly for 12 weeks.
Intervention Type
Other
Intervention Name(s)
Yoga: Active Hatha
Other Intervention Name(s)
Active
Intervention Description
Classical Hatha yoga with influences from Viniyoga and Iyengar yoga. Both Viniyoga and Iyengar yoga styles emphasize modifications and adaptations including the use of props such as straps and blocks in order to minimize the risk of injury and make the poses accessible to people with health problems and limitations
Intervention Type
Other
Intervention Name(s)
Yoga: Restorative
Other Intervention Name(s)
Non-Active
Intervention Description
Restorative Yoga is a slow-paced yoga style that emphasizes relaxation and includes very little movement.
Primary Outcome Measure Information:
Title
Pain Interference
Description
Brief Pain Inventory (BPI) : Self-Report measure of pain interference and pain severity consisting of 14 items. The measure includes front and back body diagrams to describe areas of pain, four pain severity items and seven pain interference items rated on 0-10 scales, and one question about percentage of pain relief by analgesics. The pain interference score is the mean of the 7 interference items. The pain severity score is the mean of 4 severity items. Scale scores are the mean of relevant items. Thus, scores range from 0-10 with higher scores indicating more pain interference.
Time Frame
assessed at baseline, 12 weeks, and 6 months; baseline and 12 weeks reported
Secondary Outcome Measure Information:
Title
Roland-Morris Disability Questionnaire
Description
Self-report measure consisting of 23 questions that ask about limitations experienced for a variety of daily activities. Scale scores are the sum of items endorsed, thus scores range from 0-23 with higher scores indicating more back pain-related disability.
Time Frame
assessed at baseline, 12 weeks, and 6 months; baseline and 12 weeks reported
Title
BPI Pain Severity
Description
Brief Pain Inventory (BPI) : Self-Report measure of pain severity consisting of 4 items. The measure includes front and back body diagrams to describe areas of pain, four pain severity items and seven pain interference items rated on 0-10 scales, and one question about percentage of pain relief by analgesics. The pain severity score is the mean of 4 severity items. Scale scores are the mean of relevant items. Thus, scores range from 0-10 with higher scores indicating greater pain severity.
Time Frame
assessed at baseline, 12 weeks, and 6 months; baseline and 12 weeks reported
Title
Neck Disability Index
Description
Ten-item self-report measure to assess neck pain interference in daily life activities. Each of the 10 items is scored from 0 - 5. The items are summed and scores range from 0-50 with higher scores indicating greater disability due to neck pain.
Time Frame
assessed at baseline, 12 weeks, and 6 months; baseline and 12 weeks reported
Other Pre-specified Outcome Measures:
Title
Health Related Quality of Life (HRQOL) Short-form 12 (SF12) - Physical
Description
12-Item self-report measure on individual's views about their physical health. Scores are scaled to range from 0-100 with higher scores indicating better physical quality of life.
Time Frame
assessed at baseline, 12 weeks, and 6 months; baseline and 12 weeks reported
Title
HRQOL - SF12 - Mental Health
Description
Mental Component Score for the SF12 Scores are scaled to range from 0-100 with higher scores indicating better mental quality of life.
Time Frame
assessed at baseline, 12 weeks, and 6 months; baseline and 12 weeks reported
Title
The Fatigue Severity Scale (FSS)
Description
The Fatigue Severity Scale (FSS) assesses the impact and severity of fatigue with 9 items. A score of > 4.0 constitutes severe fatigue.The measure has good psychometrics for pain disorders. This is a 9-item questionnaire with questions related to how fatigue interferes with certain activities and severity according to a self-report scale. The items are scored on a 7 point scale with 1 = strongly disagree and 7= strongly agree. The minimum score = 9 and maximum score possible = 63. Higher the score indicate greater fatigue severity.
Time Frame
assessed at baseline, 12 weeks, and 6 months; baseline and 12 weeks reported
Title
CES-D 10
Description
Ten-item self-report measure on the frequency of mood symptoms. Scores greater than or equal to 10 indicate depression. The 10 items are rated on a Likert scale from 0-3. Thus the total score ranges from 0-30 with higher scores indicating more depression.
Time Frame
assessed at baseline, 12 weeks, and 6 months; baseline and 12 weeks reported
Title
AUDIT-C
Description
The AUDIT-C is a 3-item alcohol screen that reliably identifies patients who are hazardous drinkers or have alcohol use disorders. The AUDIT-C is a modified version of the 10 question AUDIT instrument.
Time Frame
baseline, 12-weeks, 6-months
Title
Dimensions of Anger Reactions (DAR)
Description
Developed by Forbes et al., The Dimensions of Anger Reactions questionnaire consists of 7 items and has demonstrated strong internal reliability and concurrent validity with other existing measures of anger.
Time Frame
baseline, 12-weeks, 6-months
Title
The Brief Resilience Scale (BRS)
Description
The Brief Resilience Scale (BRS) assesses and individuals ability to recover from stress or trauma. The measure consists of six items and has good reliability and validity. The score is the mean of the 6 items, which are rated from 1 to 5. Scores range from 1-5.0 and higher scores indicate greater resilience.
Time Frame
baseline, 12-weeks, 6-months
Title
Self Efficacy for Chronic Low Back Pain Scale
Description
A 6-item self-report measure of an individual's confidence in performing certain activities. Items range from 1 (not at all confident) to 10 (totally confident). The score is the mean of the items and ranges from 1-10 with higher scores indicating greater self-efficacy.
Time Frame
baseline, 12-weeks, 6-months
Title
Physical Measures: Grip Strength
Description
Grip strength will be measured with a hydraulic dynamometer. Two trials will be performed for each hand and the best performance will be taken for each side. The average of both hands is used for analysis.
Time Frame
baseline, 12-weeks, 6-months
Title
Physical Measures: Core Stabilization
Description
Prone and supine bridge positions will assess core stabilization. Participants begin on their elbows in the prone position with shoulders, hips, and ankles aligned. The supine position is tested next, with knees flexed 90 degrees and pelvis raised from the floor with shoulders, hips, and knees aligned. Assessors record length of time (120 seconds max) that each position is held in proper form.
Time Frame
baseline, 12-weeks, 6-months
Title
Physical Measures: Balance
Description
Balance will be measures performance on a one-leg stand on each side. Assessors record length of time (2 minutes max) that each one-leg stand is held in proper form.
Time Frame
baseline, 12-weeks, 6-months
Title
PROMIS - Pain Intensity
Description
PROMIS (Patient-Reported Outcomes Measurement Information System) measure - Pain Intensity The PROMIS Pain Intensity instrument consists of three items with 5 response options ranging from 1 ("had no pain") to 5 ("very severe") addressing how much pain the person experiences now and in the past 7 days. The raw score is the sum of the three questions, with a minimum of 3 and a maximum score of 15, with higher scores indicating greater pain intensity.
Time Frame
assessed at baseline, 12 weeks, and 6 months; baseline and 12 weeks reported

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of CLBP or CNP > 6 months Willing to attend a yoga program for 12 weeks Willing to complete 3 assessments English literacy Have had no changes in pain treatments in the past month Willing to not change pain treatments during study unless medically necessary Have not practiced yoga more than 2x in the last 12 months Exclusion Criteria: Back or neck surgery within the last year Back or neck pain due to specific systemic problem (e.g., lupus, scoliosis) Severe vertebral disk problems, Persistent sciatica or nerve compression > 3 months Coexisting chronic pain problem (e.g., migraine headaches, fibromyalgia) Serious or unstable psychiatric illness (e.g., psychosis, mania, episode, or substance dependence) Major coexisting medical illness (e.g., cancer, COPD, morbid obesity) Positive Romberg test (with or without sensory neuropathy)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Erik Groessl, Ph.D.
Organizational Affiliation
University of California, San Diego
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ian Fowler, MD
Organizational Affiliation
Navy Medical Center San Diego
Official's Role
Principal Investigator
Facility Information:
Facility Name
UCSD's Health Services Research Center
City
San Diego
State/Province
California
ZIP/Postal Code
92121
Country
United States
Facility Name
Navy Medical Center San Diego
City
San Diego
State/Province
California
ZIP/Postal Code
92134
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35734420
Citation
Groessl EJ, Casteel D, McKinnon S, McCarthy A, Schmalzl L, Chang DG, Fowler IM, Park CL. Comparing Types of Yoga for Chronic Low Back and Neck Pain in Military Personnel: A Feasibility Randomized Controlled Trial. Glob Adv Health Med. 2022 Jun 16;11:2164957X221094596. doi: 10.1177/2164957X221094596. eCollection 2022. Erratum In: Glob Adv Integr Med Health. 2023 Mar 15;12:27536130231161197. Glob Adv Integr Med Health. 2023 Jul 17;12:27536130231187738.
Results Reference
derived

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Overcoming Pain Through Yoga in the Military

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