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Persian Gulf SyndromeCARENCT06716411

Confirming the Effects of Acupuncture Treatments to Relieve Symptoms of Gulf War Illness

A study testing Acupuncture in people with Persian Gulf Syndrome and Gulf War Syndrome, run by University of Utah at 10 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This unblinded Phase II clinical trial will test the effects of individualized acupuncture treatments offered in extant acupuncture practices in the community; practitioners will have had at least 5 years of experience plus additional training provided by the study. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Acupuncture
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
200 participants
Where
10 sitesUnited States
Study dates
3 Feb 2026to 30 Sep 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Deployed to the Gulf Theater of operations (as defined by 38 CFR 3.317, includes Iraq, Kuwait, Saudi Arabia, Bahrain, Qatar, the United Arab Emirates, Oman, the Gulf of Aden, the Gulf of Oman, the Persian Gulf, the Arabian Sea, the Red Sea, and the airspace above all of these locations) between August 1990 and the present date
  • Have at least 2 of the following symptoms from the 3 CDC clusters of symptom that have lasted for more than 6 months. Each symptom cluster must be characterized as mild-moderate or severe, with at least one symptom in each cluster required to be severe. The clusters are:
  • Fatigability: fatigue 24 hours or more after exertion B. Mood and Cognition: feeling depressed; feeling irritable; difficulty thinking or concentrating; feeling worried, tense, anxious; problems finding words; or problems getting to sleep C. Musculoskeletal: joint pain or muscle pain

Who cannot join

  • Currently enrolled in another clinical trial
  • Have another disease that likely could account for the symptoms, as determined by our Medical Monitor
  • Severe psychiatric illness (in the last 2 years psychiatric hospitalization, suicidal attempt, alcohol or substance abuse, use of antipsychotic medication) as measured by the Primary Care Evaluation of Mental Disorder (Prime MD).
  • Unable to complete the protocol on based on the evaluation of the Medical Monitor.

Trial locations and contacts

10 sites in 1 country. Contact the study team or a site near you to ask about taking part.

10 sites in 1 country

United States10 sites, 10 recruiting
  • University of California, Berkeley

    Berkeley, California, 94720

    Irina Conboy, PhD

    Not yet recruiting
  • Beth Israel Deaconess Medical Center

    Boston, Massachusetts, 02215

    Lisa A Conboy, MA MS ScD, 617-718-1917, lisa_conboy@hms.harvard.edu

    Not yet recruiting
  • Various

    Colorado Springs, Colorado, 80911

    CARE Study Research Team, 801-646-8308, gwi@utah.edu

    Not yet recruiting
  • Various

    Dallas, Texas, 75231

    CARE Study Research Team, 801-646-8308, GWI@utah.edu

    Recruiting
  • Various

    Denver, Colorado, 80203

    CARE Study Research Team, 801-646-8308, GWI@utah.edu

    Not yet recruiting
  • Various

    Fairfax, Virginia, 23235

    CARE Study Research Team, 801-646-8308, gwi@utah.edu

    Not yet recruiting
  • Various

    Los Angeles, California, 90015

    CARE Study Research Team, 801-646-8308, gwi@utah.edu

    Recruiting
  • University of Utah

    Salt Lake City, Utah, 84111

    Lisa Taylor-Swanson, lisa.taylor-swanson@nurs.utah.edu

    Not yet recruiting
  • Various

    Seattle, Washington, 98116

    CARE Study Research Team, 801-646-8308, gwi@utah.edu

    Not yet recruiting
  • Various

    Tampa, Florida, 33762

    CARE Study Research Team, 801-646-8308, GWI@utah.edu

    Recruiting

Other trials in United States

About this study

This unblinded Phase II clinical trial will test the effects of individualized acupuncture treatments offered in extant acupuncture practices in the community; practitioners will have had at least 5 years of experience plus additional training provided by the study. Veterans with diagnosed symptoms of Gulf War Illness will be randomized to either six months of biweekly acupuncture treatments (group 1, n=100) or 2 months of waitlist followed by weekly acupuncture treatments (group 2, n=100). Measurements were taken at baseline, 2, 4 and 6 months. The primary outcome is the SF-36 physical component scale score (SF-36P).

Read the detailed description

Gulf War Illness (GWI), or chronic multisymptom illness (CMI), is a complex illness characterized by multiple symptoms, including fatigue, sleep and mood disturbances, cognitive dysfunction, and musculoskeletal pain, which are unexplained by physical and laboratory examinations. There is no standard of care treatment for this syndrome at this time. First defined by the Centers for Disease Control and Prevention (CDC) after the first Gulf War, it is commonly seen with a highly individualistic presentation, associated with clusters of symptoms and co-morbid medical diagnoses, including chronic fatigue syndrome, fibromyalgia, irritable bowel syndrome, arthralgia, digestive complaints, and mood-related psychiatric disorders, including depression, posttraumatic stress disorder (PTSD), and other anxiety disorders. It has been shown to be remarkably stable at 5- and 10- year follow-ups. Of the 700,000 service personnel deployed to the Persian Gulf, 100,000 veterans of the first Gulf War (Operation Desert Shield/Storm, years 1990-1991) have presented with medical complaints through clinical and registry programs. GWI is twice as prevalent in deployed veterans, and seen in 15% of non-deployed veterans.

CMI symptoms have been studied in cohorts of veterans in the United Kingdom, Canada, and Australia. The etiology of CMI is still unknown, and hypotheses involving exposures to vaccines, medications, pesticides, chemical munitions, and inhalation of depleted uranium dust and smoke from burning oil fields, have all been investigated inconclusively. Stress plays a likely role in the etiology of other multisymptom illnesses, such as irritable bowel syndrome (IBS), multiple chemical sensitivity and chronic headache. It is likely that veterans of the current war in Iraq and Afghanistan are exposed to similar deployment stressors and will benefit from an investigation of CMI and its treatment.

Acupuncture is an evidence-based, nonpharmacologic treatment commonly used for many symptoms affecting veterans and active military personnel, including pain. Acupuncture has shown efficacy for a variety of painful musculoskeletal disorders, as a treatment for both acute and chronic pain after amputation in military contexts, and in the treatment of related comorbidities such as fatigue, state, trait and situational anxiety, and depression. Acupuncture has shown effectiveness and is used in the Veterans Health Administration (VHA) and covered by Medicare for some conditions.

The L Conboy lab has completed multiple successful acupuncture trials in areas such as Irritable Bowel Syndrome, Carpel Tunnel Syndrome, and pelvic pain. Most recently the study team successfully completed a 3.5-year Congressionally Directed Medical Research Program (CDMRP) randomized controlled trial (RCT) "The Effectiveness of Acupuncture in the Treatment of Gulf War Illness". In that study, veterans chose a trained study acupuncturist in a location convenient to them. These community-based acupuncturists provided personalized acupuncture in a therapeutically informed dose. In the robust sample (n=104), investigators found a clinically and statistically significant improvement in pain after 2 months of treatment. After 6 months of treatment McGill Pain Scale values showed a 6-point improvement (p<=0.001), and the physical component of the SF-36 (SF-36P) showed a 9-point improvement (p<=0.003). Investigators also found statistically and clinically improvements in: the severity of veterans' self-reported main (p<0.01) and secondary (p<0.009) complaints as measured by the patient-centered Measure Your Medical Outcomes Profile (MYMOP) outcome measure, self-reported overall health from the SF-36P (p<0.007), and fatigue (p<0.05) based on the Multidimensional Assessment of Fatigue. Patient satisfaction with care and confidence in treatment was also very high (95% rated satisfied and confident). In addition, investigators found that the theoretically informed dose (2 sessions per week for 6 months) provided more relief for pain and poor function than did the comparison dose of one session per week, and that over 95% of symptom improvement for pain was maintained at 5-year follow up. Acupuncture at a sufficient dose is one of the only treatments found to be effective in improving pain and function in this hard-to-treat population while also addressing other symptoms in the patient's biopsychosocial presentation. Other high-quality science has shown that dosage is important for acupuncture treatment, and that treatment effects can persist long after acupuncture treatment has ended.

While this clinical data is very promising, equally important is furthering the understanding of the mechanisms of Gulf War Illness and successful treatments. Investigators conducted blood biomarker analyses using the collected blood samples from the parent trial, including collaborations with the Boston Biorepository, Recruitment and Integrative Network (BBRAIN) consortium at Boston University. Investigators found a number of interesting contrasts including significantly altered ether lipid metabolism in GWI, and that acyl-carnitine molecules are decreased in GWI, in agreement with previous reports. More recently, in collaboration with anti-aging researchers at Berkeley, investigators have found that acupuncture at the proper dose shifts the protein signature of GWI veteran to resemble a younger state (see below). In order to further elucidate the mechanisms underlying both GWI and successful treatments, the collection of blood biomarkers will be augmented by collection of physiological biomarkers potentially implicated in GWI symptoms.

Autonomic dysregulation has been demonstrated to be common among Veterans with GWI, according to both self-report and objective measures. The 31-item Composite Autonomic Symptom Score (COMPASS-31) scale assesses autonomic dysregulation. COMPASS-31 scores were positively associated with physical function in a GWI population, with gastrointestinal (GI) symptoms as the autonomic subscale most strongly correlated. A pilot study using heart rate variability (HRV) measurement reported parasympathetic activity (PNS) negatively associated with GWI symptoms, while sympathetic nervous system activity (SNS) was positively associated with symptoms. Further, some data suggest that treatment improvements in those with GWI are associated with improvements in autonomic regulation. For example, yoga and breathing techniques have demonstrated in multiple studies in veterans and non-veterans improvements in symptoms associated with GWI, including autonomic symptoms, chronic pain, and irritable bowel syndrome. Exploration of autonomic dysregulation in this study of acupuncture for GWI is thus proposed because acupuncture is associated with decreased autonomic symptoms. A recent meta-analysis concluded that real acupuncture has a superior effect over placebo acupuncture in increasing parasympathetic tone, though this has yet to be studied in GWI.

Gastrointestinal problems and fatigue are also highly prevalent among veterans with GWI. Autonomic dysregulation among veterans with GWI has been studied with respect to gastroparesis as demonstrated by a composite autonomic score of 3.7 in veterans with GI symptoms (vs 1.3 in controls) (p<0.01). Previous work on GWI and HRV on the outcome of fatigue found a significant negative relationship between root mean square of successive differences of beat-to-beat intervals (RMSSD), a measure of PNS activity, and fatigue [r = -.0574]. This is consistent with literature indicating decreased parasympathetic activity to be a characteristic feature of both acute and daily levels of fatigue. Other work on acupuncture and HRV on the outcome of fatigue supports the investigation that acupuncture treatment is associated with decreased autonomic symptoms. Further a recent meta-analysis concluded that real acupuncture has a superior effect over placebo acupuncture in increasing parasympathetic tone, though this has yet to be studied in GWI. One study of acupuncture demonstrated decreased fatigue among patients with Chronic Fatigue Syndrome, and also reported instantaneous changes of HR after acupuncture therapy was administered.

If investigators confirm the previous clinical results, this data set will provide valuable documentation of the clinical, biological, and physiological changes that occur as veterans with GWI move to a healthier state. This will greatly improve current understanding of the Whole Health of GWI veterans, with applications to other clinical modalities and illnesses.

Subjects will be recruited via local advertisements and direct mailing to veterans on the Gulf War Registry, who live in one of the 6 areas identified by the team to have greater density of veterans diagnosed with Gulf War Illness. Through questionnaires, physician assessment, and medical histories, the investigators measured the severity of symptoms before beginning treatment, and after 2, 4 and 6 months of treatment. One group of patients received acupuncture evaluation and treatment twice per week for 6 months. A second group, for comparison purposes, will be monitored on a wait list for 2 months, and will then be offered weekly acupuncture for 4 months. The primary comparison is the difference at 6 months. Based on previous acupuncture research on fatigue, stress, and pain, including the parent study, the investigators expect this length of treatment will be enough for patients to receive significant benefit. The investigators also planed to collect samples of blood from the volunteers that will help identify possible disease mechanisms for the illness and track the effects of treatment.

Being tested
Acupuncture
Keywords
Acupuncture, Gulf War Illness, Complex Medical Illness, Chronic Multisymptom Illness, Veteran
Medical subject headings
Persian Gulf Syndrome, Multiple Chronic Conditions, Occupational Diseases, War-Related Injuries, Wounds and Injuries

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • AcupunctureDevice

    Sterile insertive needles are applied by licensed, experienced practitioners.

Study groups in NCT06716411
Study groupRoleWhat they receive
Bi-weekly acupuncture treatmentExperimentalBi-weekly acupuncture treatment
Receives: Device: Acupuncture
Wait listActive comparatorWait list for 2 months followed by weekly acupuncture for 4 months
Receives: Device: Acupuncture

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. SF-36P

    Ten items addressing physical functioning which are part of a short-form health survey with 36 questions. Scores range between 0 and 100 with higher scores indicating better function.

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Dec 2024
  2. Study start3 Feb 2026
  3. Primary completion30 Sep 2027 (estimated)
  4. Study completion30 Sep 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
200 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06716411
Sponsor's protocol ID
TX230133
Other IDs
CDMRP-TX230133P2
Acronym
CARE
Status last verified
Apr 2026
First submitted
16 Aug 2024
Last updated
3 Apr 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
Yes

Questions about this trial

What is this clinical trial studying?

A study testing Acupuncture in people with Persian Gulf Syndrome and Gulf War Syndrome, run by University of Utah at 10 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 3 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 10 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Lisa Conboy (617-718-1917, lisa_conboy@hms.harvard.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

SF-36P (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Apr 2026.

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