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
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakAdatok 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.