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| ID | Type | Description | Link |
|---|---|---|---|
| I21RX003611 | U.S. NIH Grant/Contract | View source |
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The objectives of this VA SPiRE application are to develop a combined neuromodulation and yoga (iTBS+yoga) intervention for Veterans with mild traumatic brain injury (mTBI) and chronic pain, assess the intervention's feasibility and acceptability, and to gather preliminary clinical outcome data on quality of life, function and pain that will guide future studies. This SPiRE project will directly benefit Veterans and VA Services by developing a new, non-pharmacological neurorehabilitation treatment for Veterans with mTBI and chronic pain in need of non-opioid treatment options. Neuromodulation is now offered at 30 VA hospitals and yoga is among the complementary and integrative health programs being rolled out as a part of VAs Whole Health implementation efforts. Thus, should iTBS+yoga ultimately prove to be efficacious, VA facilities will be well-poised to offer this treatment. A novel, activity-based, non-pharmacological treatment for Veterans with mTBI and chronic pain is of great need given the high prevalence of chronic pain.
Over 340,000 people have incurred a mild traumatic brain injury (mTBI) as a result of the military conflicts in Iraq and Afghanistan. mTBI leads to a host of poor rehabilitation outcomes including impairments in cognition, physical health, and psychological health. These impairments among people with TBI lead to poor quality of life (QOL). Worsening this clinical picture, the prevalence of chronic pain is estimated to be 51.5% among civilians with TBI and 43.1-70% among Veterans with TBI. Opioids are used for treating chronic pain including among people with TBI. Thus, given the ongoing opioid epidemic in the United States, it is very timely to develop alter-native, non-pharmacologic treatments for chronic pain among Veterans with mTBI. Yoga is a promising activity-based intervention for TBI and chronic pain. Yoga is an activity generally comprised of breathing exercises, gentle stretching, and meditation. Neuromodulation through transcranial magnetic stimulation (TMS) is a prom-ising non-invasive, non-pharmacological treatment for TBI and chronic pain. Intermittent theta burst stimulation (iTBS) is a type of patterned, excitatory TMS. iTBS can induce a window of neuroplasticity, making it ideally suited to boost the effects of treatments provided after it. Thus, iTBS shows promise to prime the brain for combined interventions and may magnify the impacts that these interventions would have when used alone, in order to boost outcomes. The purpose of this SPiRE project is to develop a novel, combined neuromodulation and yoga neurorehabilitation intervention for Veterans with mTBI and chronic pain, and to examine the intervention's feasibility and acceptability. Using an existing, evidence-based, yoga program created specifically for people with TBI (LoveYourBrain Yoga), the investigators will first develop a neurorehabilitation intervention that combines iTBS with yoga (iTBS+yoga), and then collect pilot data about its feasibility and acceptability. Aim 1 will develop a novel, combined iTBS+yoga neurorehabilitation intervention for Veterans with mTBI and chronic pain. Aim 2 will examine the feasibility and acceptability of the iTBS+yoga intervention for Veterans with mTBI and chronic pain. Aim 3 will gather preliminary data to provide the foundation for sample size and power considerations for a future clinical trial to examine the effectiveness of iTBS+yoga on Veterans' quality of life, function and pain out-comes. The combined intervention will be provided in small group settings once a week for 6 weeks. iTBS will be administered immediately prior to the LoveYourBrain Yoga session. Emphasizing National Institute of Neuro-logical Disorders and Stroke (NINDS) Traumatic Brain Injury Common Data Elements (TBI CDEs), the investigators will collect preliminary outcome data related to quality of life, function and pain to inform a future Merit application, should the intervention prove feasible. This SPiRE project will directly benefit Veterans and VA Services by developing a new, non-pharmacological neurorehabilitation treatment for Veterans with mTBI and chronic pain in need of non-opioid treatment options. TMS is now offered at 30 VA hospitals nationwide for treatment-resistant depression, and yoga is among the complementary and integrative health programs being rolled out as a part of VAs nation-wide Whole Health implementation efforts, with classes offered through VA service lines such as recreational therapy. Therefore, should iTBS+yoga ultimately prove to be efficacious and effective, VA facilities will be well-poised to offer this treatment. A novel, activity-based, non-pharmacological treatment for Veterans with mTBI and chronic pain is of great need given the high prevalence of chronic pain, increased risk of opioid therapy, and increased risk of developing opioid use disorders.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| iTBS+yoga | Experimental | Participants will receive 6 sessions of intermittent theta burst stimulation (iTBS) and the LoveYourBrain Yoga program. The LoveYourBrain Yoga program was specifically designed for people with TBI. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Magventure MagProx100 with MagOption | Device | The Magventure C-B60 butterfly coil will be used for single-pulse TMS to determine motor threshold. iTBS will be delivered utilizing the MagVentrure MagPro X100 with MagOption stimulator that includes active and placebo coils (C-B65 Butterfly coils) or active-only Cool-B65 Butterfly (figure 8) coil. Only the active setting will be used. |
| Measure | Description | Time Frame |
|---|---|---|
| Session Completion Rate | For feasibility, we will track the number of iTBS+yoga sessions completed and compute completion percentage rates for each participant as a metric of feasibility. | Endpoint - after last iTBS+yoga session, approximately 6 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Mayo-Portland Adaptability Index - Total | The Mayo-Portland Adaptability Index is a TBI Common Data Element assessment of function and participation. It includes 35 items each scored on a scale of 0 to 4, with 0 meaning no problems (better), and 4 meaning severe problems (worse). Minimum (best) score would be 0 and maximum (worst) score would be 140. | Endpoint (after last iTBS+yoga treatment, approximately 6 weeks) |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Amy A Herrold, PhD BA | Edward Hines Jr. VA Hospital, Hines, IL | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Edward Hines Jr. VA Hospital, Hines, IL | Hines | Illinois | 60141-3030 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 35704372 | Derived | Krese KA, Donnelly KZ, Etingen B, Bender Pape TL, Chaudhuri S, Aaronson AL, Shah RP, Bhaumik DK, Billups A, Bedo S, Wanicek-Squeo MT, Bobra S, Herrold AA. Feasibility of a Combined Neuromodulation and Yoga Intervention for Mild Traumatic Brain Injury and Chronic Pain: Protocol for an Open-label Pilot Trial. JMIR Res Protoc. 2022 Jun 15;11(6):e37836. doi: 10.2196/37836. |
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A de-identified data set will be created and shared.Final data sets will be made available as per Hines VA Hospital local policy for long term storage and access until enterprise-level resources become available. These data will be available upon request by researchers and scientists in accordance with federal guidelines and Hines local policy.
The data provided will be sufficient for anyone to perform analogous or supplemental analyses that would permit validation of the analysis and results. The sharing of data will enable others to evaluate the data and to validate and interpret the data independently. In order to insure that replication is possible and transparency, statistical code complementary to datasets will be made available through the Federal Interagency Traumatic Brain Injury Research Informatics System.
After primary publication of study data.
These data will be available upon request by researchers and scientists in accordance with federal guidelines and Hines local policy.
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Participants were screened over the phone with a delimited set of measures but more in-depth screening for full eligibility criteria occurred after consent/enrollment. Thus, only enrolled participants meeting full eligibility criteria were allowed to move forward and assigned to receive the treatment intervention.
We recruited treatment-seeking Veterans from Edward Hines Jr., VA Hospital Recruitment Period: 6/2021 to 6/2023 Types of Location: Suburban VA Hospital and associated relevant clinics such as the Polytrauma/TBI clinic.
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| ID | Title | Description |
|---|---|---|
| FG000 | iTBS+Yoga | Participants will receive 6 sessions of intermittent theta burst stimulation (iTBS) and the LoveYourBrain Yoga program. The LoveYourBrain Yoga program was specifically designed for people with TBI. Magventure MagProx100 with MagOption: The Magventure C-B60 butterfly coil will be used for single-pulse TMS to determine motor threshold. iTBS will be delivered utilizing the MagVentrure MagPro X100 with MagOption stimulator that includes active and placebo coils (C-B65 Butterfly coils) or active-only Cool-B65 Butterfly (figure 8) coil. Only the active setting will be used. |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
19 participants enrolled, 14 initiated iTBS+yoga sessions, and 10 completed all sessions
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| ID | Title | Description |
|---|---|---|
| BG000 | Open Label iTBS+Yoga | All patients received individual approximately 3-minute iTBS session followed by a 90-minute group LoveYourBrain yoga session. iTBS+yoga sessions occurred once a week for 6 weeks. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Session Completion Rate | For feasibility, we will track the number of iTBS+yoga sessions completed and compute completion percentage rates for each participant as a metric of feasibility. | 14 participants initiated iTBS+yoga treatment sessions and could possibly complete 6 total number of intervention sessions. Thus total number of possible sessions is 14 x 6 = 84 | Posted | Count of Units | number of sessions | Endpoint - after last iTBS+yoga session, approximately 6 weeks | number of sessions | number of sessions |
|
6 weeks
Safety data on safety indicators was collected at each iTBS session including the following: hypertension, hypotension, heart rate, oxygen saturation, sleep, fatigue medication changes, seizure, headache/neck pain, fever, fainting, scalp/skin breakdown, tinnitus, dizziness, nausea, vomiting, confusion, and contraindicated substance use.
Adverse event reporting logs were completed and reported to the IRB.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Open Label iTBS+Yoga | All patients received individual approximately 3-minute iTBS session followed by a 90-minute group LoveYourBrain yoga session. iTBS+yoga sessions occurred once a week for 6 weeks. |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| headache | Nervous system disorders | Systematic Assessment | 3 individuals had headaches, resulting in 1 participant self-withdrawing. For this person, the headaches started ~3 days after the first session. This participant had a history of occasional unlocalized headaches. |
The main limitations were the small sample size, open-label design, and lack of a control group. As this was a pilot we did not assess for multiple comparisons. Our satisfaction ratings and qualitative interviews assessing acceptability may be biased as they were only done for those completing all 6 intervention sessions.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr. Amy Herrold | Edward Hines Jr., VA Hospital | 708-202-5867 | amy.herrold@va.gov |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Feb 1, 2022 | Sep 18, 2024 | Prot_SAP_002.pdf |
| ICF | No | No | Yes | Informed Consent Form | Feb 23, 2022 | Sep 18, 2024 | ICF_003.pdf |
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| ID | Term |
|---|---|
| D001924 | Brain Concussion |
| D059350 | Chronic Pain |
| D000070642 | Brain Injuries, Traumatic |
| D010146 | Pain |
| ID | Term |
|---|---|
| D001930 | Brain Injuries |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
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Intermittent Theta Burst Stimulation (iTBS) in combination with Love Your Brain Yoga Program. 6 weekly sessions of iTBS given prior to small group yoga.
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| Brief Pain Inventory - Pain Severity | The Brief Pain Inventory is a self-report measure of pain symptoms throughout the body. It has 4 main items and each item is scored on a scale of 0 to 10 with 0 meaning no pain (better), and 10 meaning pain as bad as you can imagine (worse). Minimum (best) score would be 0 and maximum (worst) score would be 40. | Endpoint (after last iTBS+yoga treatment, approximately 6 weeks) |
| Participants |
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| Age, Continuous | Mean | Full Range | years |
|
| Sex/Gender, Customized | Count of Participants | Participants |
|
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
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| Race (NIH/OMB) | Count of Participants | Participants |
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| Region of Enrollment | Count of Participants | Participants |
|
| Brief Pain Inventory - Pain Severity | 4 main items and each item is scored on a scale of 0 to 10 with 0 meaning no pain, and 10 meaning pain as bad as you can imagine. Minimum (best) score for all 4 items would be 0 and maximum (worst) score would be 40. | All participants that completed baseline assessments are included which is an n=14. | Mean | Standard Deviation | units on a scale |
|
| Brief Pain Inventory - Pain Interference | 7 main items and each item is scored on a scale of 0 to 10 with 0 meaning does not interfere, and 10 meaning completely interferes. Minimum (best) score for all 7 items would be 0 and maximum (worst) score would be 70. | All participants who completed baseline measures are included which is an n=14. | Mean | Standard Deviation | units on a scale |
|
| Mayo-Portland Adaptability Inventory (MPAI-4) - Total | Mayo-Portland Adaptability Inventory (MPAI-4) Total T-Score. The Total raw score is converted to a T-score using a national sample conversion chart provided in the MPAI-4 manual. Mean = 50, Standard deviation = 10. Higher scores represent worse function and lower scores indicate better function. | All participants who participated in baseline assessments are reported which is an n=14. | Mean | Standard Deviation | T-Score |
|
| Mayo-Portland Adaptability Inventory (MPAI-4) - Ability | Mayo-Portland Adaptability Inventory (MPAI-4) Ability Index Subscale T-Score. The Ability Index Subscale raw score is converted to a T-score using a national sample conversion chart provided in the MPAI-4 manual. Mean = 50, Standard deviation = 10. Higher scores represent worse function and lower scores indicate better function. | All participants who completed baseline assessments are included which is an n=14. | Mean | Standard Deviation | T-Score |
|
| Mayo-Portland Adaptability Inventory (MPAI-4) - Participation | Mayo-Portland Adaptability Inventory (MPAI-4) Participation Index Subscale T-Score. The Participation Index Subscale raw score is converted to a T-score using a national sample conversion chart provided in the MPAI-4 manual. Mean = 50, Standard deviation = 10. Higher scores represent worse function and lower scores indicate better function. | All participants who completed baseline assessments which is an n=14 are included. | Mean | Standard Deviation | T-Score |
|
| Mayo-Portland Adaptability Inventory (MPAI-4) - Adjustment | Mayo-Portland Adaptability Inventory (MPAI-4) Adjustment Index Subscale T-Score. The Adjustment Index Subscale raw score is converted to a T-score using a national sample conversion chart provided in the MPAI-4 manual. Mean = 50, Standard deviation = 10. Higher scores represent worse function and lower scores indicate better function. | All participants that completed baseline assessments are included which is an n=14. | Mean | Standard Deviation | T-Score |
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| Secondary | Mayo-Portland Adaptability Index - Total | The Mayo-Portland Adaptability Index is a TBI Common Data Element assessment of function and participation. It includes 35 items each scored on a scale of 0 to 4, with 0 meaning no problems (better), and 4 meaning severe problems (worse). Minimum (best) score would be 0 and maximum (worst) score would be 140. | Analysis completed on the 10 iTBS+yoga treatment completers | Posted | Mean | Standard Deviation | score on a scale | Endpoint (after last iTBS+yoga treatment, approximately 6 weeks) |
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| Secondary | Brief Pain Inventory - Pain Severity | The Brief Pain Inventory is a self-report measure of pain symptoms throughout the body. It has 4 main items and each item is scored on a scale of 0 to 10 with 0 meaning no pain (better), and 10 meaning pain as bad as you can imagine (worse). Minimum (best) score would be 0 and maximum (worst) score would be 40. | Analysis completed on the 10 iTBS+yoga treatment completers | Posted | Mean | Standard Deviation | score on a scale | Endpoint (after last iTBS+yoga treatment, approximately 6 weeks) |
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| 0 |
| 19 |
| 0 |
| 19 |
| 3 |
| 19 |
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| D006259 |
| Craniocerebral Trauma |
| D020196 | Trauma, Nervous System |
| D016489 | Head Injuries, Closed |
| D014947 | Wounds and Injuries |
| D014949 | Wounds, Nonpenetrating |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |