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Translational Research Examining Acupuncture Treatment in Traumatic Brain Injury (TREAT-TBI)

Primary Purpose

Traumatic Brain Injury

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Acupuncture
Sham Acupuncture
Sponsored by
AOMA Graduate School of Integrative Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Traumatic Brain Injury focused on measuring traumatic brain injury, acupuncture, transcranial doppler ultrasound

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age 18-50
  • Documented TBI (for TBI-ACUP and TBI-SHAM arms)
  • Visual acuity and hearing adequate for outcomes testing
  • Fluency in English
  • Ability to provide informed consent
  • Acupuncture naïve

Exclusion Criteria:

  • Significant polytrauma that may interfere with follow-up and outcome assessment
  • Patients with major debilitating baseline mental health disorders that would interfere with the validity of outcome assessment due to TBI
  • Patients on psychiatric hold
  • Patients with major debilitating baseline neurological diseases impairing baseline awareness, cognition, or validity of outcome assessment due to TBI
  • Significant history of pre-existing conditions that would interfere with the likelihood of follow-up and validity of outcome assessment due to TBI
  • Pregnancy in female subjects
  • Prisoners or patients in custody
  • Current participation in an observational or intervention trial for TBI
  • Non-English speakers

Sites / Locations

  • Healing Response Acupuncture & Integrative Medicine

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm Type

Experimental

Sham Comparator

Active Comparator

Sham Comparator

Active Comparator

Arm Label

TBI-ACUP

TBI-SHAM

C-ACUP

C-SHAM

C-EX

Arm Description

This group will receive the standard of care plus acupuncture treatments during the acute 10-day phase following a diagnosed TBI.

This group will receive the standard of care plus sham acupuncture treatments during the acute 10-day phase following a diagnosed TBI.

This group of participants without TBI will receive one acupuncture treatment and serve as a healthy control group.

This group of participants will receive one sham acupuncture treatment and serve as a healthy sham comparator group.

This group of participants without TBI will receive one acupuncture treatment following 30-60 minutes of aerobic exercise, and serve as a healthy control group.

Outcomes

Primary Outcome Measures

Cerebral Blood Flow Velocity in the Left (L) and Right (R) Middle Cerebral Artery (MCA), Internal Carotid Artery (ICA), and Basilar Artery (BA).
Cerebral blood flow velocity was assessed at baseline, post-fight, and post-acupuncture in the TBI-ACUP arm. Cerebral blood flow velocity was assessed at baseline, post fight, and post-sham acupuncture in the TBI-SHAM arm. Cerebral blood flow velocity was assessed at baseline, post exercise, and post-acupuncture in the C-EX arm. Cerebral blood flow velocity was assessed at baseline, and post-acupuncture in the C-ACUP arm. Cerebral blood flow velocity was assessed at baseline, and post-sham acupuncture in the C-SHAM arm.

Secondary Outcome Measures

Changes in Hopkins Verbal Learning Test
The Hopkins Verbal Learning Test consists of a 12-item word list, composed of four words from each of three semantic categories which the patient must learn over three trials. For each trial, the subject is instructed to listen carefully as the examiner reads the word list and attempt to memorize the words. The score for total recall is the sum of all the correctly-recalled words from each trial, ranging from 0 to 36, with higher scores indicating better recall and retention.
Rivermead Post-Concussion Survey
The Rivermead Post-Concussion Symptoms Questionnaire (RPQ) is a 16-item survey that assesses the severity of the most common post-concussion symptoms on a scale of 0 to 4, with a total score range from 0 to 64 with 64 denoting the greatest symptom severity").

Full Information

First Posted
December 3, 2015
Last Updated
January 20, 2020
Sponsor
AOMA Graduate School of Integrative Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT02623218
Brief Title
Translational Research Examining Acupuncture Treatment in Traumatic Brain Injury
Acronym
TREAT-TBI
Official Title
Translational Research Examining Acupuncture Treatment in Traumatic Brain Injury
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
November 2015 (undefined)
Primary Completion Date
May 2016 (Actual)
Study Completion Date
May 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AOMA Graduate School of Integrative Medicine

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to examine the effects of acupuncture on cerebral blood flow (CBF) and blood biomarkers during the acute 10-day window following traumatic brain injury, to determine if those changes correlate with changes in biomarkers of brain health, neuropsychological testing, and symptomatic presentation.
Detailed Description
The primary aim of this study is to examine the effects of acupuncture on brain function and cognition during the acute 10-day window following mild traumatic brain injury. Traumatic brain injuries (TBI) affect an estimated 1.7 to 2.3 million Americans every year. As the clinical importance of managing those with TBI grows, it is essential that therapies to help in the recovery and management of post-concussion symptoms are identified. Currently, the number one recommended treatment strategy is physical and cognitive rest, followed by gradual return to daily activities and exercise. Cerebral blood flow declines following TBI, and can remain in a depressed state for ongoing lengths of time. The cellular vulnerability and symptomatic presentation following TBI is likely due to the metabolic imbalance between decreased cerebral blood flow and increased demand for glucose and adenosine triphosphate production. Animal and human studies have shown that acupuncture at locations both locally on the head and neck, as well as distally on the arms, hands, legs, and feet, can increase cerebral blood flow through the left (L) and right (R) middle cerebral artery (MCA), internal carotid artery (ICA), and basilar artery (BA). Acupuncture has a long history of use in the treatment of acute and chronic pain, headaches, migraines, nausea, anxiety, and sleep disorders, however, studies specific to the utilization of acupuncture in managing symptoms following TBI are lacking. The investigators hypothesize that that acupuncture treatments may improve cerebral blood flow resulting in overall improvements in brain function and cognition following TBI. Acupuncture may provide a safe treatment to improve outcomes following a TBI, and increase the rate of recovery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Traumatic Brain Injury
Keywords
traumatic brain injury, acupuncture, transcranial doppler ultrasound

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
22 (Actual)

8. Arms, Groups, and Interventions

Arm Title
TBI-ACUP
Arm Type
Experimental
Arm Description
This group will receive the standard of care plus acupuncture treatments during the acute 10-day phase following a diagnosed TBI.
Arm Title
TBI-SHAM
Arm Type
Sham Comparator
Arm Description
This group will receive the standard of care plus sham acupuncture treatments during the acute 10-day phase following a diagnosed TBI.
Arm Title
C-ACUP
Arm Type
Active Comparator
Arm Description
This group of participants without TBI will receive one acupuncture treatment and serve as a healthy control group.
Arm Title
C-SHAM
Arm Type
Sham Comparator
Arm Description
This group of participants will receive one sham acupuncture treatment and serve as a healthy sham comparator group.
Arm Title
C-EX
Arm Type
Active Comparator
Arm Description
This group of participants without TBI will receive one acupuncture treatment following 30-60 minutes of aerobic exercise, and serve as a healthy control group.
Intervention Type
Device
Intervention Name(s)
Acupuncture
Intervention Description
An acupuncture needle is a device intended to pierce the skin in the practice of acupuncture. The device consists of a solid, stainless steel needle. The device may have a handle attached to the needle to facilitate the delivery of acupuncture treatment.
Intervention Type
Device
Intervention Name(s)
Sham Acupuncture
Other Intervention Name(s)
Streitberger Needle
Intervention Description
Sham acupuncture will be performed at the same locations as verum acupuncture. Streitberger sham acupuncture needles look like real acupuncture needles, and appear as though the skin is being penetrated during the insertion technique, however they do not pierce the skin.
Primary Outcome Measure Information:
Title
Cerebral Blood Flow Velocity in the Left (L) and Right (R) Middle Cerebral Artery (MCA), Internal Carotid Artery (ICA), and Basilar Artery (BA).
Description
Cerebral blood flow velocity was assessed at baseline, post-fight, and post-acupuncture in the TBI-ACUP arm. Cerebral blood flow velocity was assessed at baseline, post fight, and post-sham acupuncture in the TBI-SHAM arm. Cerebral blood flow velocity was assessed at baseline, post exercise, and post-acupuncture in the C-EX arm. Cerebral blood flow velocity was assessed at baseline, and post-acupuncture in the C-ACUP arm. Cerebral blood flow velocity was assessed at baseline, and post-sham acupuncture in the C-SHAM arm.
Time Frame
At baseline, post-fight, post-exercise (up to 5 hours from baseline), post acupuncture/post sham acupuncture (within 3 hours from baseline)
Secondary Outcome Measure Information:
Title
Changes in Hopkins Verbal Learning Test
Description
The Hopkins Verbal Learning Test consists of a 12-item word list, composed of four words from each of three semantic categories which the patient must learn over three trials. For each trial, the subject is instructed to listen carefully as the examiner reads the word list and attempt to memorize the words. The score for total recall is the sum of all the correctly-recalled words from each trial, ranging from 0 to 36, with higher scores indicating better recall and retention.
Time Frame
At baseline, post-fight, post-exercise, and post-acupuncture/sham acupuncture
Title
Rivermead Post-Concussion Survey
Description
The Rivermead Post-Concussion Symptoms Questionnaire (RPQ) is a 16-item survey that assesses the severity of the most common post-concussion symptoms on a scale of 0 to 4, with a total score range from 0 to 64 with 64 denoting the greatest symptom severity").
Time Frame
Post-fight, Post-Acupuncture/Sham - TBI-ACUP and TBI-SHAM groups only

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age 18-50 Documented TBI (for TBI-ACUP and TBI-SHAM arms) Visual acuity and hearing adequate for outcomes testing Fluency in English Ability to provide informed consent Acupuncture naïve Exclusion Criteria: Significant polytrauma that may interfere with follow-up and outcome assessment Patients with major debilitating baseline mental health disorders that would interfere with the validity of outcome assessment due to TBI Patients on psychiatric hold Patients with major debilitating baseline neurological diseases impairing baseline awareness, cognition, or validity of outcome assessment due to TBI Significant history of pre-existing conditions that would interfere with the likelihood of follow-up and validity of outcome assessment due to TBI Pregnancy in female subjects Prisoners or patients in custody Current participation in an observational or intervention trial for TBI Non-English speakers
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John Finnell, ND
Organizational Affiliation
AOMA Graduate School of Integrative Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Amy Moll, M.A.O.M.
Organizational Affiliation
AOMA Graduate School of Integrative Medicine
Official's Role
Study Director
Facility Information:
Facility Name
Healing Response Acupuncture & Integrative Medicine
City
Dallas
State/Province
Texas
ZIP/Postal Code
75214
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21417808
Citation
Byeon HS, Moon SK, Park SU, Jung WS, Park JM, Ko CN, Cho KH, Kim YS, Bae HS. Effects of GV20 acupuncture on cerebral blood flow velocity of middle cerebral artery and anterior cerebral artery territories, and CO2 reactivity during hypocapnia in normal subjects. J Altern Complement Med. 2011 Mar;17(3):219-24. doi: 10.1089/acm.2010.0232. Epub 2011 Feb 27.
Results Reference
background
PubMed Identifier
25226574
Citation
Im JW, Moon SK, Jung WS, Cho KH, Kim YS, Park TH, Ko CN, Park JM, Park SU, Cho SY. Effects of acupuncture at GB20 on CO2 reactivity in the basilar and middle cerebral arteries during hypocapnia in healthy participants. J Altern Complement Med. 2014 Oct;20(10):764-70. doi: 10.1089/acm.2013.0240. Epub 2014 Sep 16.
Results Reference
background
PubMed Identifier
19848545
Citation
An YS, Moon SK, Min IK, Kim DY. Changes in regional cerebral blood flow and glucose metabolism following electroacupuncture at LI 4 and LI 11 in normal volunteers. J Altern Complement Med. 2009 Oct;15(10):1075-81. doi: 10.1089/acm.2009.0257.
Results Reference
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Translational Research Examining Acupuncture Treatment in Traumatic Brain Injury

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