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

VA Office of Research and Development logo

VA Office of Research and Development

Status

Completed

Conditions

Sleeplessness
Brain Injuries, Traumatic

Treatments

Other: Acupuncture
Other: Sham Acupuncture

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT01162317
B6924-W

Details and patient eligibility

About

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.

Enrollment

60 patients

Sex

All

Ages

18 to 55 years old

Volunteers

No 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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Double Blind

60 participants in 2 patient groups

Arm 1: sham acupuncture
Active Comparator group
Description:
sham acupuncture
Treatment:
Other: Sham Acupuncture
Arm 2: acupuncture
Experimental group
Description:
acupuncture
Treatment:
Other: Acupuncture

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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