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AcuSleep in Mild Traumatic Brain Injury (TBI)

Novel Approaches to Sleep Difficulties: Application in Mild TBI

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01162317
Acronym
AcuTBI
Enrollment
60
Registered
2010-07-14
Start date
2011-07-05
Completion date
2017-12-18
Last updated
2018-01-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain Injuries, Traumatic, Sleeplessness

Keywords

Acupuncture, Sleep, Traumatic brain injury

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.

Interventions

OTHERAcupuncture

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.

OTHERSham Acupuncture

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.

Sponsors

VA Office of Research and Development
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
PSQI ChangeBaseline and post-interventionchange 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

MeasureTime frameDescription
Wrist Actigraphy (an Objective Sleep Measure) Sleep Efficiencypre-intervention, post-intervention (1wk of recording each)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%.

Countries

United States

Participant flow

Participants by arm

ArmCount
Arm 1: Sham Acupuncture
sham acupuncture Sham Acupuncture: 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.
30
Arm 2: Acupuncture
acupuncture Acupuncture: 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.
30
Total60

Baseline characteristics

CharacteristicArm 1: Sham AcupunctureArm 2: AcupunctureTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
30 Participants30 Participants60 Participants
Age, Continuous40 years
STANDARD_DEVIATION 10.3
39.6 years
STANDARD_DEVIATION 9.7
39.8 years
STANDARD_DEVIATION 10
Pittsburgh Sleep Quality Index (PSQI)14.33 units on a scale
STANDARD_DEVIATION 3.1
14.17 units on a scale
STANDARD_DEVIATION 3.41
14.26 units on a scale
STANDARD_DEVIATION 3.2
Region of Enrollment
United States
30 Participants30 Participants60 Participants
Sex: Female, Male
Female
8 Participants6 Participants14 Participants
Sex: Female, Male
Male
22 Participants24 Participants46 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
3 / 308 / 30
serious
Total, serious adverse events
0 / 300 / 30

Outcome results

Primary

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.

Time frame: Baseline and post-intervention

ArmMeasureValue (MEAN)Dispersion
Arm 1: Sham AcupuncturePSQI Change-2.38 change of points from baselineStandard Deviation 3.41
Arm 2: AcupuncturePSQI Change-4.43 change of points from baselineStandard Deviation 3.86
Secondary

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%.

Time frame: pre-intervention, post-intervention (1wk of recording each)

Population: All obtained actigraphy data were analyzed. This form doesn't allow specific indication of sample sizes. Therefore, here overall numbers of participants analyzed were the same as the maximal potential.

ArmMeasureGroupValue (MEAN)Dispersion
Arm 1: Sham AcupunctureWrist Actigraphy (an Objective Sleep Measure) Sleep EfficiencyPre-intervention73.57 percentageStandard Deviation 13.21
Arm 1: Sham AcupunctureWrist Actigraphy (an Objective Sleep Measure) Sleep EfficiencyPost-intervention67.94 percentageStandard Deviation 13.28
Arm 2: AcupunctureWrist Actigraphy (an Objective Sleep Measure) Sleep EfficiencyPre-intervention72.57 percentageStandard Deviation 16.41
Arm 2: AcupunctureWrist Actigraphy (an Objective Sleep Measure) Sleep EfficiencyPost-intervention76.68 percentageStandard Deviation 12.18

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026