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Résztvevőt keres itt: Egyesült Államok3. fázis

Cannabidiol-Assisted Learning for Managing Generalized Anxiety Disorder

A legfontosabb adatok

Ki végzi
Wayne State University
Hol
Detroit (Egyesült Államok)A helyszín megnézése
Azonosító
Állapot
Toboroz
Fázis
3. fázis
Résztvevők
90 fő, tervezett
Kezdés
2025. nov. 3.
Várható befejezés
2027. aug. 31.
A vizsgálat típusa
Beavatkozással járó, 4 csoportAz egyik csoport placebót (hatóanyag nélküli szert) kap, összehasonlításként.
A vizsgált kezelések
  • Low-Dose Cannabidiol
  • Placebo Matched to Moderate-Dose Cannabidiol
  • Moderate-Dose Cannabidiol
  • Placebo Matched to Low-Dose Cannabidiol
A regiszteradat frissítve
2026. október 21.

Ki vehet részt

Életkor
18 év – 45 év
Nem
Nők és férfiak
Egészséges önkéntesek
Nem vehetnek részt

A regiszter feltételei, szó szerint

Mind a 29 feltétel megnézéseKevesebb

Ki vehet részt

  • Right-handed
  • Age 18-45 years at enrollment
  • Able to consent to the study
  • Agree to adhere to lifestyle considerations throughout study duration
  • Generally medically and neurologically healthy, including no evidence of intellectual disability or serious cognitive impairment
  • Have a current generalized anxiety disorder (GAD) diagnosis according to the The Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria and/or total scores ≥ 8 on the 7-Item Generalized Anxiety Disorders Scale (GAD-7)

Ki nem vehet részt

  • Positive drug screen or alcohol breathalyzer
  • Receiving concurrent psychotherapy or have received psychotherapy, including for research purposes, within the past year
  • Use of medications known to have severe drug interactions with cannabidiol or that are strong inducers of cytochrome P450 3A4 (CYP3A4) or cytochrome P450 2C19 (CYP2C19)
  • Use of as needed anti-anxiety medications (e.g., benzodiazepines), unstable dose of other psychoactive drug (i.e., < 4 weeks), or intention to start new treatment during this trial
  • Current or past-month use of cannabis, or a tetrahydrocannabinol (THC) or cannabidiol-containing product (self-report and urine drug screen)
  • Treatment with another investigational drug or intervention within the past month
  • Clinically significant medical or neurologic condition or neurocognitive dysfunction that would affect function and/or task performance and/or interfere with the study protocol
  • Any current (or within past 2 months) medical condition requiring medication that would interact with cannabidiol or interfere with the study protocol
  • Presence of contraindications, current or past allergic or adverse reaction, or known sensitivity to cannabinoid-like substances or components of EPIDIOLEX®
  • Current moderate or severe alcohol/drug use disorder or in the past 8 weeks
  • Current or past diagnosis of bipolar and other related disorders, schizophrenia spectrum, or other psychotic disorders
  • Visual impairment
  • Current or past-month coronavirus disease 2019 (COVID-19) diagnosis or febrile illness
  • Under 18 or over 45 years of age
  • Risk of harm to self or others that requires immediate intervention
  • Unwilling/unable to sign informed consent document
  • Currently pregnant (positive pregnancy test), planning pregnancy, or lactating (women),
  • Traumatic brain injury, as defined by The American Congress of Rehabilitation as a person who has had a traumatically induced physiological disruption of brain function (i.e., the head being struck, the head striking an object, and/or the brain undergoing an acceleration/deceleration movement [i.e., whiplash] without direct external trauma to the head), as manifested by at least one of the following: any loss of consciousness; any loss of memory for events immediately before or after the injury; any alteration in mental status at the time of the incident; or focal neurological deficits that may or may not be transient)
  • Inability to tolerate small, enclosed spaces without anxiety (e.g. claustrophobia), as determined by self-report and/or a preliminary session in a mock scanner
  • Presence of ferrous-containing metals within the body (e.g., aneurysm clips, shrapnel/retained particles)
  • GAD-7 score < 8
  • Baseline labs 3 times outside of normal range
  • Difficulty with or inability to comply with the complete clinical trial

Nézd meg, megfelelhetsz-e

Magadról válaszolj. Ez nem döntés: hogy részt vehetsz-e, azt csak a vizsgálat csapata mondhatja meg.

  • 18 és 45 év között vagy?

Helyszínek itt: Egyesült Államok

  • Wayne State University School of Medicine, Tolan Park Medical BuildingDetroit, Egyesült ÁllamokContact: Hilary Marusak, PhDRésztvevőt keres

A vizsgálatról

Mit akar kideríteni a vizsgálat

This randomized, double-blind, placebo-controlled clinical trial investigates the use of Food and Drug Administration (FDA)-approved cannabidiol (EPIDIOLEX®) as an adjunct to cognitive behavioral therapy (CBT) in adults with generalized anxiety disorder (GAD). The study aims to evaluate whether cannabidiol-assisted CBT enhances emotion regulation via dorsomedial prefrontal cortex (dmPFC) activation and improves anxiety symptom outcomes compared to CBT with placebo.

A vizsgálat 4 csoportja

  • Brief Cognitive Behavioral Therapy + Moderate-Dose CannabidiolA vizsgált kezelés

    Participants will receive a 5-week course of brief cognitive behavioral therapy (CBT) combined with oral cannabidiol (EPIDIOLEX®) at a moderate dose. Dosing starts at 5 milligram/kilogram/day and titrates to 10 milligram/kilogram/day (divided twice a day) after 6 days. Cannabidiol is administered chronically throughout CBT to examine target engagement and symptom outcomes.

    Kezelés: Moderate-Dose Cannabidiol

  • Brief Cognitive Behavioral Therapy + Low-Dose CannabidiolA vizsgált kezelés

    Participants will receive a 5-week course of brief cognitive behavioral therapy (CBT) combined with a lower dose of oral cannabidiol (EPIDIOLEX®), maintained at 5 milligram/kilogram/day (divided twice a day) throughout the treatment period. No titration is required.

    Kezelés: Low-Dose Cannabidiol

  • Brief Cognitive Behavioral Therapy + Placebo Titrated to Match Moderate-Dose CannabidiolPlacebo, összehasonlításként

    Participants will receive a 5-week course of brief cognitive behavioral therapy (CBT) combined with a matched placebo oral solution. The placebo mimics the appearance, smell, and taste of EPIDIOLEX®. For blinding the moderate dose cannabidiol arm, dosing starts at 5 milligram/kilogram/day and titrates to 10 milligram/kilogram/day (divided twice a day) after 6 days.

    Kezelés: Placebo Matched to Moderate-Dose Cannabidiol

  • Brief Cognitive Behavioral Therapy + Placebo Titrated to Match Low-Dose CannabidiolPlacebo, összehasonlításként

    Participants will receive a 5-week course of brief cognitive behavioral therapy (CBT) combined with a matched placebo oral solution. The placebo mimics the appearance, smell, and taste of EPIDIOLEX®. For blinding the low-dose cannabidiol arm, dosing is maintained at 5 milligram/kilogram/day (divided twice a day) throughout the treatment period. No titration is required.

    Kezelés: Placebo Matched to Low-Dose Cannabidiol

Kérdések a vizsgálat csapatának

  1. Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
  2. Megtérítik az utazási költséget?
  3. Megtarthatom a saját orvosomat?
  4. Mi történik, ha ki akarok lépni?

Contact the study team: see the registry record → Contacts and Locations

Oldal nyomtatása az orvosomnak

Adatok és források

Regiszteradat
Szerepel a ClinicalTrials.gov-on.
Hivatalos cím
Cannabidiol-Enhanced Cognitive Behavioral Therapy for Generalized Anxiety Disorder
Illeszkedési kérdések
Forrás: NCT07123467: ki vehet részt
A regiszteradat frissítve
2026. október 21.