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Lo studio clinico NCT06716411 (CARE) per Persian Gulf Syndrome, Sindrome della guerra del Golfo, Multiple Chronic Illnesses, Malattie professionali, War-Related Injuries, Ferite e lesioni è in arruolamento. Consulti la vista a schede del Radar degli Studi Clinici e gli strumenti di scoperta IA per tutti i dettagli. Oppure, ponga pure una domanda qui.
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Confirming the Effects of Acupuncture Treatments to Relieve Symptoms of Gulf War Illness (CARE) 200 Randomizzato Veterani

In arruolamento
I dettagli dello studio clinico sono disponibili principalmente in inglese. Tuttavia, Trial Radar IA può essere d'aiuto! Basta cliccare su 'Spiega lo studio' per visualizzare e discutere le informazioni sullo studio nella lingua selezionata.
La sperimentazione clinica NCT06716411 (CARE) è uno studio interventistico per Persian Gulf Syndrome, Sindrome della guerra del Golfo, Multiple Chronic Illnesses, Malattie professionali, War-Related Injuries, Ferite e lesioni, attualmente in arruolamento. Avviato il 3 febbraio 2026, prevede di arruolare 200 partecipanti. Sotto la guida di l'Università dello Utah, dovrebbe concludersi entro il 30 settembre 2028. I dati più recenti da ClinicalTrials.gov sono stati aggiornati l'ultima volta il 11 febbraio 2026.
Sommario breve
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 mon...Mostra di più
Descrizione dettagliata
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)...Mostra di più
Titolo ufficiale

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

Patologie
Persian Gulf SyndromeSindrome della guerra del GolfoMultiple Chronic IllnessesMalattie professionaliWar-Related InjuriesFerite e lesioni
Altri ID dello studio
  • CARE
  • TX230133
  • TX230133 (Altro numero di finanziamento) (Department of the Army)
Numero NCT
NCT06716411
Data di inizio (effettiva)
2026-02-03
Ultimo aggiornamento pubblicato
2026-02-11
Data di completamento (stimata)
2028-09-30
Arruolamento (previsto)
200
Tipo di studio
Interventistico
FASE
N.D.
Stato
In arruolamento
Parole chiave
Acupuncture
Gulf War Illness
Complex Medical Illness
Chronic Multisymptom Illness
Veteran
Scopo principale
Trattamento
Allocazione
Randomizzato
Modello di intervento
In parallelo
Mascheramento
Doppio
Bracci / Interventi
Gruppo/Braccio di partecipantiIntervento/Trattamento
SperimentaleBi-weekly acupuncture treatment
Bi-weekly acupuncture treatment
Agopuntura
Sterile insertive needles are applied by licensed, experienced practitioners.
Comparatore attivoWait list
Wait list for 2 months followed by weekly acupuncture for 4 months
Agopuntura
Sterile insertive needles are applied by licensed, experienced practitioners.
Esito primario
Misure di esitoDescrizione della misuraArco temporale
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.
6 months
Assistente alla partecipazione
Criteri di eleggibilità

Età idonea
Adulto, Adulto anziano
Età minima
18 Years
Sessi idonei
Tutti
  • 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:

A. 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

  • 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.
University of Utah logoUniversità dello Utah304 studi clinici attivi da esplorare
Parte responsabile dello studio
Lisa J Taylor-Swanson, Investigatore principale, Principal Investigator, PhD, University of Utah
Contatti principali dello studio
Contatto: Lisa Conboy, 617-718-1917, [email protected]
10 Centri dello studio in 1 paesi

California

University of California, Berkeley, Berkeley, California, 94720, United States
Irina Conboy, PhD, Contatto
Non ancora in arruolamento
Various, Los Angeles, California, 90015, United States
CARE Study Research Team, Contatto, 801-646-8308, [email protected]
In arruolamento

Colorado

Various, Colorado Springs, Colorado, 80911, United States
CARE Study Research Team, Contatto, 801-646-8308, [email protected]
Non ancora in arruolamento
Various, Denver, Colorado, 80203, United States
CARE Study Research Team, Contatto, 801-646-8308, [email protected]
Non ancora in arruolamento

Florida

Various, Tampa, Florida, 33762, United States
CARE Study Research Team, Contatto, 801-646-8308, [email protected]
In arruolamento

Massachusetts

Beth Israel Deaconess Medical Center, Boston, Massachusetts, 02215, United States
Lisa A Conboy, MA MS ScD, Contatto, 617-718-1917, [email protected]
Non ancora in arruolamento

Texas

Various, Dallas, Texas, 75231, United States
CARE Study Research Team, Contatto, 801-646-8308, [email protected]
In arruolamento

Utah

University of Utah, Salt Lake City, Utah, 84111, United States
Lisa Taylor-Swanson, Contatto, [email protected]
Non ancora in arruolamento

Virginia

Various, Fairfax, Virginia, 23235, United States
CARE Study Research Team, Contatto, 801-646-8308, [email protected]
Non ancora in arruolamento

Washington

Various, Seattle, Washington, 98116, United States
CARE Study Research Team, Contatto, 801-646-8308, [email protected]
Non ancora in arruolamento