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Strength and Awareness in Action: an Intervention for Post-Acute TBI Headaches (SAA-TBI) (SAA-TBI)

Primary Purpose

Traumatic Brain Injury, Post-concussive Headaches

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
SAA-TBI
Sponsored by
VA Eastern Colorado Health Care System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Traumatic Brain Injury focused on measuring Yoga, Veterans, Traumatic Brain Injury, Post-concussive Headaches, Post-concussive Symptoms

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Between the ages of 18 and 55
  • Able to provide informed consent
  • History of mTBI per the Ohio State University TBI-ID (OSU-TBI-ID)
  • History of PCH pain (TTH, migraine, or mixed), with onset of pain or increase in previous headache pain having occurred within one month of mTBI as determined by structured examination using criteria outlined in the International Classification of Headache Disorders-3 beta (ICHD-3 beta)
  • Duration of PCH pain being greater than one year as determined by structured medical examination
  • Score of >49 on the Headache Impact Test-6 (HIT-6)
  • Medical clearance by study provider to participate in yoga protocol

Exclusion Criteria:

  • Younger than 18, or older than 55 years of age
  • Active substance dependence, excluding Cannabis dependence (based on local issues regarding the legality of cannabis), as determined by structured clinical interview
  • Moderate to severe TBI as determined per the OSU-TBI-ID
  • Identification of active psychosis as determined by structured clinical interview
  • Failing to receive medical clearance by study provider;
  • Inability to participate in the manualized intervention without postures being significantly modified
  • Already participating in an ongoing consistent yoga practice (two or more times weekly)
  • Involvement in another research interventional trial aimed at addressing pain-related symptoms.

Sites / Locations

  • Rocky Mountain Regional VA Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

YOGA-NOW

YOGA-WAIT

Arm Description

Participant will start the SAA-TBI (yoga) about 2 weeks (+/- 2 weeks) after Study Visit 3.

Participant will start SAA-TBI (yoga) about 10 weeks (+/- 2 weeks) after Study Visit 3.

Outcomes

Primary Outcome Measures

Headaches per week
Headache Tracking Form (HTF) will query about daily headache frequency, duration, severity, and treatment per event.

Secondary Outcome Measures

Full Information

First Posted
September 7, 2017
Last Updated
July 22, 2019
Sponsor
VA Eastern Colorado Health Care System
Collaborators
University of Colorado, Denver
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1. Study Identification

Unique Protocol Identification Number
NCT03277859
Brief Title
Strength and Awareness in Action: an Intervention for Post-Acute TBI Headaches (SAA-TBI)
Acronym
SAA-TBI
Official Title
Strength and Awareness in Action: an Intervention for Post-Acute TBI Headaches (SAA-TBI)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
August 16, 2017 (Actual)
Primary Completion Date
June 30, 2019 (Actual)
Study Completion Date
June 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
VA Eastern Colorado Health Care System
Collaborators
University of Colorado, Denver

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
The specific aims of the proposed study are to evaluate: 1) the feasibility of design elements of a Strength and Awareness in Action: an Intervention for Post-Acute TBI Headaches (SAA-TBI) intervention trial (e.g., an exercise run-in to facilitate participant retention); 2) yoga instructor fidelity; and 3) variability estimates for candidate proximal and distal outcomes. Performance of validated measures, including those associated with quality of life, as well as data collected via ecological momentary assessment and pedometry (physical activity) will be evaluated.
Detailed Description
A signature injury being sustained by Veterans from recent conflicts is mild traumatic brain injury (mTBI). For some, this condition is associated with multiple disabling post-concussive symptoms, including post-concussive headaches (PCH). PCHs are notoriously resistant to medication alone, and are associated with increased muscle tension, avoidance of physical activities, and anxiety related to having chronic pain. In this study, the feasibility (ease of implementation) of the design elements of an interventional trial of Strength and Awareness in Action: an Intervention for Post-Acute TBI Headaches (SAA-TBI) will be explored. Yoga is operationalized as a practice involving physical postures, breath awareness, breathing exercises and mindfulness meditation. It is conceptualized as having three "active ingredients" (i.e., regulation of the autonomic nervous system via physical activity/breathing exercises, release of muscular tension associated with headaches, and mindfulness/acceptance). The specific aims of the proposed study are to evaluate: 1) the feasibility of design elements of an SAA-TBI intervention trial (e.g., an exercise run-in to facilitate participant retention); 2) yoga instructor fidelity; and 3) variability estimates for candidate proximal and distal outcomes. Performance of validated measures, including those associated with quality of life, as well as data collected via ecological momentary assessment and pedometry (physical activity) will be evaluated. Project aims will be evaluated using an experimental design where participants will be block randomized in a stratified manner to SAA-TBI or a waitlist using a 1:1 ratio. The waitlist group will initially receive 8 weeks of enhanced treatment as usual (ETU). The participants in the waitlist condition will be offered SAA-TBI, after the initial group has completed the intervention. Both groups of participants will complete multiple measures at baseline and after the conclusion of the intervention. Maintenance among the intervention group will also be explored. Participants will be asked to complete daily homework documenting their headaches and yoga practice outside of class, and be provided with multiple modalities (web-based, mobile app, text, or paper and pencil) by which this can be accomplished. In specific, the proposed study will evaluate the feasibility of the trial design for an accessible, non-pharmacological, yoga-based intervention for chronic PCH pain among Veterans with mTBI, with the long-term goal of informing future efficacy trials.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Traumatic Brain Injury, Post-concussive Headaches
Keywords
Yoga, Veterans, Traumatic Brain Injury, Post-concussive Headaches, Post-concussive Symptoms

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Participants will be block randomized in a stratified manner to SAA-TBI or a waitlist using a 1:1 ratio. The waitlist group will initially receive 8 weeks of enhanced treatment as usual (ETU).
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
75 (Actual)

8. Arms, Groups, and Interventions

Arm Title
YOGA-NOW
Arm Type
Experimental
Arm Description
Participant will start the SAA-TBI (yoga) about 2 weeks (+/- 2 weeks) after Study Visit 3.
Arm Title
YOGA-WAIT
Arm Type
Active Comparator
Arm Description
Participant will start SAA-TBI (yoga) about 10 weeks (+/- 2 weeks) after Study Visit 3.
Intervention Type
Behavioral
Intervention Name(s)
SAA-TBI
Intervention Description
Yoga twice a week for 75 minutes for 8 weeks
Primary Outcome Measure Information:
Title
Headaches per week
Description
Headache Tracking Form (HTF) will query about daily headache frequency, duration, severity, and treatment per event.
Time Frame
Change from baseline to approximately 20 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Between the ages of 18 and 55 Able to provide informed consent History of mTBI per the Ohio State University TBI-ID (OSU-TBI-ID) History of PCH pain (TTH, migraine, or mixed), with onset of pain or increase in previous headache pain having occurred within one month of mTBI as determined by structured examination using criteria outlined in the International Classification of Headache Disorders-3 beta (ICHD-3 beta) Duration of PCH pain being greater than one year as determined by structured medical examination Score of >49 on the Headache Impact Test-6 (HIT-6) Medical clearance by study provider to participate in yoga protocol Exclusion Criteria: Younger than 18, or older than 55 years of age Active substance dependence, excluding Cannabis dependence (based on local issues regarding the legality of cannabis), as determined by structured clinical interview Moderate to severe TBI as determined per the OSU-TBI-ID Identification of active psychosis as determined by structured clinical interview Failing to receive medical clearance by study provider; Inability to participate in the manualized intervention without postures being significantly modified Already participating in an ongoing consistent yoga practice (two or more times weekly) Involvement in another research interventional trial aimed at addressing pain-related symptoms.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lisa A Brenner, PhD
Organizational Affiliation
VA Eastern Colorado Health Care System
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rocky Mountain Regional VA Medical Center
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States

12. IPD Sharing Statement

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Strength and Awareness in Action: an Intervention for Post-Acute TBI Headaches (SAA-TBI)

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