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Acupuncture for PTSD

Acupuncture for PTSD in Combat Veterans

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02869646
Enrollment
92
Registered
2016-08-17
Start date
2018-04-05
Completion date
2022-12-30
Last updated
2024-04-18

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

Conditions

Posttraumatic Stress Disorder

Keywords

PTSD, acupuncture, integrative medicine

Brief summary

Current treatments for Veterans with PTSD include medications and therapy where the patient talks about traumatic events in order to desensitize to them. While these treatments work for many, a large minority of Veterans do not want medications or exposure therapy. The investigators developed an acupuncture (ACU) treatment for PTSD in order to broaden treatment options. The investigators' first study showed that it helped most people. However, the investigators need better scientific evidence that it works by comparing ACU to a placebo, such as sham acupuncture (fewer needles in non-important sites) and determining if ACU alters abnormal physiology in PTSD. In this study 90 Veterans will be randomly assigned (like a coin flip) to receive either ACU or sham. The investigators expect to find that the ACU treated patients have more improvement in PTSD and in physiology (less startle reaction - assessed non-invasively using skin sensors) than the patients in the sham group. This study will provide information to support the use of acupuncture for PTSD at the VA, which will expand treatment options.

Detailed description

Posttraumatic Stress Disorder (PTSD) is debilitating and common (up to 30% in Vietnam Veterans and 16% in Afghanistan and Iraq Veterans). A significant number of Veterans do not engage in or drop-out from effective trauma-focused therapies due to avoidance from trauma-related memories. Because of this limitation, and because scientific literature suggested that acupuncture might be effective for PTSD symptoms, the investigators developed an acupuncture intervention for PTSD and conducted a clinical trial that showed positive effects. This remains the only high quality trial of acupuncture for PTSD published, because of which the current VA/DoD guidelines for PTSD state that acupuncture is a B recommendation (fair evidence, provide service) for PTSD treatment. That civilian study compared acupuncture to an effective therapy (CBT) and a wait-list control, but did not have a placebo control. And, research has shown that Veterans may respond differently to therapies than civilians. More definitive data about the efficacy of acupuncture for PTSD is required in order to recommend it as an A evidence-based intervention for PTSD in Veterans. Specifically, it is important to show that acupuncture is better than a placebo control and that it has effects on biological abnormalities of PTSD. The aim of this study is to demonstrate efficacy of acupuncture for PTSD by showing clinical and biological effects that are statistically larger and clinically more important than effects of sham acupuncture. Given current knowledge and the need for efficient, ethical and best practices within an experimental design, the primary aim is best accomplished by a randomized controlled trial comparing verum acupuncture (ACU) to placebo minimal needling sham acupuncture (MIN). The goal is to evaluate ACU for a significant positive signal, not to compare ACU to other interventions or to evaluate treatment durability. Acupuncture is delivered in 24 sessions over 12 weeks. The primary hypothesis is that efficacy of ACU for PTSD symptom severity will be large (pre- to post-treatment Cohen's d \> 0.8), and significantly better than MIN (between group Cohen's d \> 0.30, with 80% probability of detecting a true group difference at p\<0.05 (2-sided). The secondary hypothesis is that compared to MIN, ACU will be associated with a significantly larger change from pre- to post-treatment in psychophysiological response (decreased startle by EMG eyeblink during fear conditioning procedure). The study design is a two-arm, parallel-group, prospective randomized controlled trial (RCT). The sample frame is Veterans with chronic PTSD with a sample of convenience from those seeking care at the Long Beach VA. Exclusion criteria are meant to keep out individuals with characteristics that are known to be PTSD treatment confounds, associated with non-adherence or negative response to treatment, that may significantly affect biological assessment, or who may be put at risk of harm. The sample size (90) provides adequate power to test hypotheses. Subjects will be allocated to intervention group by computer-generated adaptive randomization. General linear mixed models will be used to evaluate hypothesized effects over time (mid treatment, end of treatment, 1-month follow-up), controlling for baseline severity of symptoms and demographic characteristics (e.g., age, gender) using intent-to-treat modeling. Outcome effect size (Cohen's d) within and between subjects will be calculated. Interaction terms will be included in the models to evaluate treatment fidelity and treatment expectancy as potential moderators. Study results will provide clinicians and policy makers with more information to make decisions about the rational use of acupuncture for PTSD. This is important because acupuncture is being touted for PTSD by many advocates. It has the potential to reach PTSD sufferers who are not willing to engage in trauma-focused psychotherapy, or for whom current therapies are ineffective. The objective of this project is consistent with priority research areas of specific interest to Clinical Science Research & Development (CSR&D) including PTSD and complementary medicine, and all participants are Veterans at a VA Hospital.

Interventions

PROCEDUREProcedure: Acupuncture

Acupuncture is a general term indicating the insertion and stimulation of needles at one or more prescribed points in order to effect the biology of the individual.

PROCEDUREProcedure: Sham acupuncture

Sham acupuncture is a general term indicating the use of needles, whether inserted or not, at points on the body that are not expected to have a clinically significant biological effect.

Sponsors

Analydata, Inc.
CollaboratorINDUSTRY
VA Office of Research and Development
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

Inclusion criteria are meant to recruit a relatively homogeneous yet generalizable sample of Veterans with at least moderate chronic PTSD due to combat trauma. Criteria are: * Veterans age 18 to 55 * DSM-5 criteria for chronic PTSD on the Clinician Administered PTSD Scale (CAPS-5) * At least moderate PTSD by having a total CAPS-5 score of \> 26 and meeting criteria for each of 4 symptom clusters. * Eligible persons will be allowed to have other symptoms that are commonly comorbid with PTSD. This strategy will provide a feasible and generalizable sample of those with chronic PSTD, but these will not be inclusion or

Exclusion criteria

, e.g.,: * anxiety * mild to moderate depression * Women and minorities will be recruited

Design outcomes

Primary

MeasureTime frameDescription
Change in PTSD Symptom Severity on the Clinician Administered PSTD Scale - CAPS 5 From Before to After TreatmentBaseline and 12 weeksThe Clinician Administered PTSD Scale (CAPS) (Blake et al, 1995) is a structured diagnostic interview for PTSD. The CAPS-5 based on DSM-5 criteria will be used. CAPS-5 has 20 symptom items, each rated from 0 (absent) to 4 (severe). A rating of \>2 is considered a positive score for diagnostic purposes. The DSM-5 diagnostic rule requires the presence of least one Criterion B symptom, one Criterion C symptom, two Criterion D symptoms, and two Criterion E symptoms in addition to other impairment criteria. The minimum score is 0; the maximum score is 80. A higher score is more severe symptoms and a worse outcome. A DSM-5 CAPS cutoff score of \>26 AND meeting each of the 4 symptom cluster criterion will be used for study inclusion and outcomes.

Secondary

MeasureTime frameDescription
Percentage Change From Baseline in Eyeblink Startle PotentiationBaseline, 12 weeksThe startle response, measured with electromyography (EMG) of the eyeblink, provides an ideal translational tool to investigate fear conditioning and extinction, since the amygdala is directly connected with the startle circuit. The raw EMG signal will be recorded at a rate of 1000 Hz throughout the experimental session using a 28 Hz high pass and 500 Hz low pass filter (as recommended by guidelines for human eyeblink startle in Blumenthal et al., 2005; Psychophysiology, 42:1-15). Raw signals will be stored and exported for analysis in microvolt ( V) values.

Countries

United States

Participant flow

Participants by arm

ArmCount
Verum Acupuncture
Traditional Chinese Medicine (TCM) based acupuncture at prescribed sites Procedure: Acupuncture: Acupuncture is a general term indicating the insertion and stimulation of needles at one or more prescribed points in order to effect the biology of the individual.
47
Minimal Needling
shallow and non-acupoint needles at same number of sites Procedure: Sham acupuncture: Sham acupuncture is a general term indicating the use of needles, whether inserted or not, at points on the body that are not expected to have a clinically significant biological effect.
45
Total92

Baseline characteristics

CharacteristicTotalVerum AcupunctureMinimal Needling
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
92 Participants47 Participants45 Participants
Annual Income
$0 - $19,999
13 Participants3 Participants10 Participants
Annual Income
$20,000 - 34,999
14 Participants6 Participants8 Participants
Annual Income
$35,000 - $49,999
22 Participants13 Participants9 Participants
Annual Income
>$50,000
42 Participants24 Participants18 Participants
Annual Income
Missing
1 Participants1 Participants0 Participants
Combat Exposure
Heavy
15 Participants8 Participants7 Participants
Combat Exposure
Light
3 Participants1 Participants2 Participants
Combat Exposure
Moderate
30 Participants16 Participants14 Participants
Combat Exposure
Moderate Heavy
28 Participants14 Participants14 Participants
Combat Exposure
Moderate Light
16 Participants8 Participants8 Participants
Country of Birth
Other
21 Participants12 Participants9 Participants
Country of Birth
United States
71 Participants35 Participants36 Participants
Deployment Preparedness
High
40 Participants20 Participants20 Participants
Deployment Preparedness
Low
7 Participants4 Participants3 Participants
Deployment Preparedness
Moderate
45 Participants23 Participants22 Participants
Education Level
College Degree
35 Participants17 Participants18 Participants
Education Level
HS/GED
19 Participants12 Participants7 Participants
Education Level
Some College
38 Participants18 Participants20 Participants
Employment Status
No
51 Participants30 Participants21 Participants
Employment Status
Yes
41 Participants17 Participants24 Participants
Marital Status
Divorced
21 Participants8 Participants13 Participants
Marital Status
Married
45 Participants24 Participants21 Participants
Marital Status
Other
6 Participants2 Participants4 Participants
Marital Status
Single
20 Participants13 Participants7 Participants
Race/Ethnicity, Customized
Race
American Indian/Alaskan Native
2 Participants2 Participants0 Participants
Race/Ethnicity, Customized
Race
Asian
17 Participants8 Participants9 Participants
Race/Ethnicity, Customized
Race
Black/African American
12 Participants5 Participants7 Participants
Race/Ethnicity, Customized
Race
More than one
15 Participants6 Participants9 Participants
Race/Ethnicity, Customized
Race
Other
3 Participants3 Participants0 Participants
Race/Ethnicity, Customized
Race
White
43 Participants23 Participants20 Participants
Religion
Buddhist
4 Participants3 Participants1 Participants
Religion
Christian
45 Participants22 Participants23 Participants
Religion
Muslim
2 Participants0 Participants2 Participants
Religion
None
20 Participants12 Participants8 Participants
Religion
Other
21 Participants10 Participants11 Participants
Sex: Female, Male
Female
8 Participants4 Participants4 Participants
Sex: Female, Male
Male
84 Participants43 Participants41 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 470 / 45
other
Total, other adverse events
21 / 4716 / 45
serious
Total, serious adverse events
0 / 470 / 45

Outcome results

Primary

Change in PTSD Symptom Severity on the Clinician Administered PSTD Scale - CAPS 5 From Before to After Treatment

The Clinician Administered PTSD Scale (CAPS) (Blake et al, 1995) is a structured diagnostic interview for PTSD. The CAPS-5 based on DSM-5 criteria will be used. CAPS-5 has 20 symptom items, each rated from 0 (absent) to 4 (severe). A rating of \>2 is considered a positive score for diagnostic purposes. The DSM-5 diagnostic rule requires the presence of least one Criterion B symptom, one Criterion C symptom, two Criterion D symptoms, and two Criterion E symptoms in addition to other impairment criteria. The minimum score is 0; the maximum score is 80. A higher score is more severe symptoms and a worse outcome. A DSM-5 CAPS cutoff score of \>26 AND meeting each of the 4 symptom cluster criterion will be used for study inclusion and outcomes.

Time frame: Baseline and 12 weeks

Population: t-tests, statistics of significance and power, and Cohen d tests were used to test hypotheses

ArmMeasureValue (MEAN)Dispersion
Verum AcupunctureChange in PTSD Symptom Severity on the Clinician Administered PSTD Scale - CAPS 5 From Before to After Treatment22.6 score on a scaleStandard Deviation 14.1
Minimal NeedlingChange in PTSD Symptom Severity on the Clinician Administered PSTD Scale - CAPS 5 From Before to After Treatment29.1 score on a scaleStandard Deviation 11.8
Secondary

Percentage Change From Baseline in Eyeblink Startle Potentiation

The startle response, measured with electromyography (EMG) of the eyeblink, provides an ideal translational tool to investigate fear conditioning and extinction, since the amygdala is directly connected with the startle circuit. The raw EMG signal will be recorded at a rate of 1000 Hz throughout the experimental session using a 28 Hz high pass and 500 Hz low pass filter (as recommended by guidelines for human eyeblink startle in Blumenthal et al., 2005; Psychophysiology, 42:1-15). Raw signals will be stored and exported for analysis in microvolt ( V) values.

Time frame: Baseline, 12 weeks

Population: This is only a subset since some either did not participate or dropped out of this component of the research

ArmMeasureValue (MEAN)Dispersion
Verum AcupuncturePercentage Change From Baseline in Eyeblink Startle Potentiation-55.8 % change potentiation of startleStandard Deviation 21.9
Minimal NeedlingPercentage Change From Baseline in Eyeblink Startle Potentiation6.1 % change potentiation of startleStandard Deviation 19.5

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026