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AcuSleep in Mild Traumatic Brain Injury (TBI) (AcuTBI)

Primary Purpose

Brain Injuries, Traumatic, Sleeplessness

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Acupuncture
Sham Acupuncture
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Brain Injuries, Traumatic focused on measuring Acupuncture, Sleep, Traumatic brain injury

Eligibility Criteria

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

Inclusion Criteria:

  • Age: 18 to 55; and,
  • Meeting the diagnosis criteria for mild traumatic brain injury as listed above at the time of injury; and,
  • At or over 3 months post injury; and,
  • With untreated sleep complaints (Pittsburgh Sleep Quality Index [PSQI] > 8, sleep difficulties at least 4x per week in the past month, average sleep duration of 6 hours or less); and,
  • Has the capacity to give informed consent.
  • Agree to attend 13 clinic visits

Exclusion Criteria:

  • Same sleep complaints present prior to traumatic brain injury; or,
  • Diagnosis of obstructive sleep apnea (OSA) by prior sleep study; or,
  • With a non-daytime work-schedule; or,
  • With prior acupuncture experience for the treatment of sleep difficulties or with acupuncture treatment within 3 months; or,
  • History of bleeding diathesis or currently on anticoagulation with international normalized ratio (INR) over 2.5; or,
  • Severe depression with Beck Depression Score of 29 and above; or,
  • Moderate and severe alcohol users.
  • Does not have a permanent address

Sites / Locations

  • Atlanta VA Medical and Rehab Center, Decatur, GA

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Arm 1: sham acupuncture

Arm 2: acupuncture

Arm Description

sham acupuncture

acupuncture

Outcomes

Primary Outcome Measures

PSQI Change
change of global PSQI score as compared to baseline The Pittsburgh Sleep Quality Index (PSQI) is a self-report questionnaire that assesses sleep quality over a 1-month time interval. The PSQI global score has a possible range of 0-21 points. Any score above 5 is considered insomnia. The higher the score the worse the condition.

Secondary Outcome Measures

Wrist Actigraphy (an Objective Sleep Measure) Sleep Efficiency
Wrist actigraphy is a non-invasive method of continuously monitoring gross body activities when a watch-like actimetry sensor is worn at the non-dominant wrist. An algorithm has been developed to assess sleep/wake behavior. Specifically in this study, we used Respironics® actiwatches for data collection. Subjects were asked to wear the actiwatches for a consecutive week at baseline and then at post-intervention, and the actiwatches were taken off only during showers. Wrist actigraphy was examined in association with sleep diary the subjects were to keep for the weeks of monitoring. Threshold-based method algorithm for data interpretation was provided by Respironics® Actiware Software. Medium level threshold was set to detect Wake and Sleep; sleep interval detection algorithm was set for 3 minutes of immobile minutes for Sleep Onset and 5 minutes of immobile minutes for Sleep End. Sleep efficiency is sleep duration divided by total bed time (both in minutes), times 100%.

Full Information

First Posted
June 15, 2010
Last Updated
December 19, 2017
Sponsor
VA Office of Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT01162317
Brief Title
AcuSleep in Mild Traumatic Brain Injury (TBI)
Acronym
AcuTBI
Official Title
Novel Approaches to Sleep Difficulties: Application in Mild TBI
Study Type
Interventional

2. Study Status

Record Verification Date
December 2017
Overall Recruitment Status
Completed
Study Start Date
July 5, 2011 (Actual)
Primary Completion Date
September 30, 2015 (Actual)
Study Completion Date
December 18, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Objective: To evaluate real acupuncture, as compare to sham acupuncture, in improving persistent sleep difficulties in veterans with mild traumatic brain injury (mTBI) Design: Randomized, blinded, sham-controlled clinical trial Setting: Outpatient clinic at a major VA medical center in Southeast USA Participants: Sixty veterans aged 24-55 (mean 40) with history of mTBI at least 3-month and beyond, suffering from sleep difficulties refractory to regular care and sleep education, as indicated by a global Pittsburgh Sleep Quality Index (PSQI) score of 14.25 + 3.23 pre-intervention (baseline). They were randomized into 2 groups, real acupuncture versus sham acupuncture, and stratified by Post-traumatic stress disorder (PTSD) diagnosed by PTSD CheckList - Military Version (PCL-M). Intervention: Real or sham acupuncture with both standardized and individualized acupoints selection. All subjects were informed that the treatments, if effective, may improve symptoms such as pain, anxiety or depression other than sleep; real acupuncture may not be effective in some individuals, and sham acupuncture may as well be effective by mind-body interactions. Outcome Measures: Primary outcome measure was global PSQI score change after intervention as compared to baseline. Secondary outcome measure was wrist-actigraphy sleep latency, sleep efficiency, wake after sleep onset (WASO), and sleep duration. PTSD was analyzed as a co-variant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Injuries, Traumatic, Sleeplessness
Keywords
Acupuncture, Sleep, Traumatic brain injury

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm 1: sham acupuncture
Arm Type
Active Comparator
Arm Description
sham acupuncture
Arm Title
Arm 2: acupuncture
Arm Type
Experimental
Arm Description
acupuncture
Intervention Type
Other
Intervention Name(s)
Acupuncture
Intervention Description
Treatments will be performed by the PI, who is a licensed physician acupuncturist and has practiced acupuncture independently for 5 years with about 4000 patient/visit treatment history. A total of 10 acupuncture treatments represents a reasonable approach to optimal duration of treatment. Acupoint selection will be based on a combination of standardization and individualization for best treatment effects. At least 5 standardized body and auricular acupoints will be selected. Standardized sterile, disposable acupuncture needles will be applied for 20 minutes.
Intervention Type
Other
Intervention Name(s)
Sham Acupuncture
Intervention Description
Treatments will be performed by the PI, who is a licensed physician acupuncturist and has practiced acupuncture independently for 5 years with about 4000 patient/visit treatment history. A total of 10 acupuncture treatments represent a reasonable approach to optimal duration of treatment. Acupoint selection will be based on a combination of standardization and individualization for best treatment effects. At least 5 standardized body and auricular acupoints will be selected. Standardized sterile, disposable acupuncture needles will be applied for 20 minutes. Each sham or real acupuncture needle will be applied through a tube as sham needles have blunt tip and telescopic shaft, the visual effect and percutaneous sensation of sham needle mimic the real needle penetration.
Primary Outcome Measure Information:
Title
PSQI Change
Description
change of global PSQI score as compared to baseline The Pittsburgh Sleep Quality Index (PSQI) is a self-report questionnaire that assesses sleep quality over a 1-month time interval. The PSQI global score has a possible range of 0-21 points. Any score above 5 is considered insomnia. The higher the score the worse the condition.
Time Frame
Baseline and post-intervention
Secondary Outcome Measure Information:
Title
Wrist Actigraphy (an Objective Sleep Measure) Sleep Efficiency
Description
Wrist actigraphy is a non-invasive method of continuously monitoring gross body activities when a watch-like actimetry sensor is worn at the non-dominant wrist. An algorithm has been developed to assess sleep/wake behavior. Specifically in this study, we used Respironics® actiwatches for data collection. Subjects were asked to wear the actiwatches for a consecutive week at baseline and then at post-intervention, and the actiwatches were taken off only during showers. Wrist actigraphy was examined in association with sleep diary the subjects were to keep for the weeks of monitoring. Threshold-based method algorithm for data interpretation was provided by Respironics® Actiware Software. Medium level threshold was set to detect Wake and Sleep; sleep interval detection algorithm was set for 3 minutes of immobile minutes for Sleep Onset and 5 minutes of immobile minutes for Sleep End. Sleep efficiency is sleep duration divided by total bed time (both in minutes), times 100%.
Time Frame
pre-intervention, post-intervention (1wk of recording each)

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: Age: 18 to 55; and, Meeting the diagnosis criteria for mild traumatic brain injury as listed above at the time of injury; and, At or over 3 months post injury; and, With untreated sleep complaints (Pittsburgh Sleep Quality Index [PSQI] > 8, sleep difficulties at least 4x per week in the past month, average sleep duration of 6 hours or less); and, Has the capacity to give informed consent. Agree to attend 13 clinic visits Exclusion Criteria: Same sleep complaints present prior to traumatic brain injury; or, Diagnosis of obstructive sleep apnea (OSA) by prior sleep study; or, With a non-daytime work-schedule; or, With prior acupuncture experience for the treatment of sleep difficulties or with acupuncture treatment within 3 months; or, History of bleeding diathesis or currently on anticoagulation with international normalized ratio (INR) over 2.5; or, Severe depression with Beck Depression Score of 29 and above; or, Moderate and severe alcohol users. Does not have a permanent address
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wei Huang, MD PhD
Organizational Affiliation
Atlanta VA Medical and Rehab Center, Decatur, GA
Official's Role
Principal Investigator
Facility Information:
Facility Name
Atlanta VA Medical and Rehab Center, Decatur, GA
City
Decatur
State/Province
Georgia
ZIP/Postal Code
30033
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30549498
Citation
Huang W, Johnson TM, Kutner NG, Halpin SN, Weiss P, Griffiths PC, Bliwise DL. Acupuncture for Treatment of Persistent Disturbed Sleep: A Randomized Clinical Trial in Veterans With Mild Traumatic Brain Injury and Posttraumatic Stress Disorder. J Clin Psychiatry. 2018 Dec 11;80(1):18m12235. doi: 10.4088/JCP.18m12235.
Results Reference
derived

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AcuSleep in Mild Traumatic Brain Injury (TBI)

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