Probing the Cannabinoid System in Individuals With a Family History of Psychosis

Sponsor
Yale University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT02102113
Collaborator
(none)
21
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2
119
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Study Details

Study Description

Brief Summary

The overall purpose of this study is to determine whether a family history of psychosis is associated with an altered cannabinoid system. This will be tested by studying individuals with and without a family history of psychosis and comparing their responses to delta 9-tetrahydrocannabinol (THC), a probe of the cannabinoid system. We hypothesize, that compared to controls with no family history of psychoses, individuals with a family history of psychoses will have an altered response to THC.

Condition or Disease Intervention/Treatment Phase
  • Drug: Placebo
  • Drug: Very Low Dose THC
  • Drug: Low Dose THC
Early Phase 1

Study Design

Study Type:
Interventional
Anticipated Enrollment :
21 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Double (Participant, Care Provider)
Primary Purpose:
Other
Official Title:
Probing the Cannabinoid System in Individuals With a Family History of Psychosis
Study Start Date :
Jan 1, 2014
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Other: No Family History of Psychosis (FHN)

Individuals recruited with no history of psychosis in the family. They will receive the placebo, very low dose THC, and low dose THC interventions.

Drug: Placebo
placebo

Drug: Very Low Dose THC
Subjects will receive 0.010mg/kg.
Other Names:
  • delta 9-tetrahydrocannabinol
  • Drug: Low Dose THC
    Subjects will receive 0.018 mg/kg over 20 minutes.
    Other Names:
  • delta 9-tetrahydrocannabinol
  • Experimental: Family History of Psychosis (FHP)

    Individuals with a family member with a confirmed diagnosis of psychosis. They will receive the placebo, very low dose THC, and low dose THC interventions.

    Drug: Placebo
    placebo

    Drug: Very Low Dose THC
    Subjects will receive 0.010mg/kg.
    Other Names:
  • delta 9-tetrahydrocannabinol
  • Drug: Low Dose THC
    Subjects will receive 0.018 mg/kg over 20 minutes.
    Other Names:
  • delta 9-tetrahydrocannabinol
  • Outcome Measures

    Primary Outcome Measures

    1. Positive and Negative Symptom Scale for Schizophrenia (PANSS) [-30 min from administration of THC]

      Positive, negative and general symptoms will be assessed using the positive, negative and general symptoms subscales of the PANSS.

    2. Positive and Negative Symptom Scale for Schizophrenia (PANSS) [+80 min from administration of THC]

      Positive, negative and general symptoms will be assessed using the positive, negative and general symptoms subscales of the PANSS.

    3. Positive and Negative Symptom Scale for Schizophrenia (PANSS) [+150 min of administration of THC]

      Positive, negative and general symptoms will be assessed using the positive, negative and general symptoms subscales of the PANSS.

    4. Positive and Negative Symptom Scale for Schizophrenia (PANSS) [+240 min of administration of THC]

      Positive, negative and general symptoms will be assessed using the positive, negative and general symptoms subscales of the PANSS.

    Secondary Outcome Measures

    1. Clinician Administered Dissociative Symptoms Scale (CADSS) [-30 min, +15 min, +80 min, +150 min, +240 min]

      Perceptual alterations will be measured using the CADSS. This is a scale consisting of 19 self-report items and 8 clinician-rated items (0=not at all, 4=extremely). The scale captures alterations in environmental/time/body perception, feelings of unreality, and memory impairment.

    2. Visual Analog Scale (VAS) [-30 min, +15 min, +80 min, +150 min, +240 min]

      Feeling states associated with cannabis intoxication will be measured using a self-reported visual analogue scale of four feeling states ("high", "anxious", "calm and relaxed", and "tired") associated with cannabis effects. Subjects will be asked to score the perceived intensity of these feeling states at that moment on a 11 mm line (0=not at all, 100=extremely). These data will be captured to validate that the experiment is relevant to cannabis effects.

    3. Hopkins Verbal Learning Test (HVLT) [+50 min]

      The HVLT is a 12 word list that is semantically organized. The task consists of 5 trials, an interference list, and free delayed recall and recognition. A different version of the AVLT will be administered on each test day and counterbalanced across subjects.

    4. Psychotomimetic States Inventory (PSI) [-30 min, +240 min]

      The PSI is a measure of drug induced psychotomimetic states. This self-report scale consists of 28 items rated 0 (not at all) to 3 (extremely) and will facilitate the characterization of a wide range of dissociative/hallucinatory phenomena as well as cognitive disorganization associated with the administration of THC.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 55 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria FHP:
    • Exposure to cannabis at least once in their lifetime

    • Medically and psychiatrically healthy based on screening

    • Having one relative with a confirmed psychotic disorder

    Exclusion Criteria FHP:
    • Current or lifetime major DSM-IV Axis I disorder

    • Current or lifetime treatment (at least 6 months) with psychotropic medications for major psychiatric or neurological illness

    • Major or unstable medical illness that might impact safety of the subject in the study

    • Cannabis naive

    • IQ less than 85

    • Less than a high school diploma or its educational equivalent

    • Pregnancy or lactation

    • Major current or recent (<6 weeks) psychosocial stressors.

    Inclusion Criteria FHN :
    • Exposure to cannabis at least once in their lifetime

    • Medically and psychiatrically healthy based on screening

    Exclusion Criteria FHN:
    • Having a family member with psychosis

    • Current or lifetime major DSM-IV Axis I disorder

    • Current or lifetime treatment (at least 6 months) with psychotropic medications for major psychiatric or neurological illness

    • Major or unstable medical illness that might impact safety of the subject in the study

    • Cannabis naive

    • IQ less than 85

    • Less than a high school diploma or its educational equivalent

    • Pregnancy or lactation

    • Major current or recent (<6 weeks) psychosocial stressors.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 VA Connecticut Healthcare System West Haven Connecticut United States 06516

    Sponsors and Collaborators

    • Yale University

    Investigators

    • Principal Investigator: Mohini Ranganathan, MD, Yale University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Mohini Ranganathan, Assistant Professor of Psychiatry, Yale University
    ClinicalTrials.gov Identifier:
    NCT02102113
    Other Study ID Numbers:
    • 1310012948
    First Posted:
    Apr 2, 2014
    Last Update Posted:
    Jul 22, 2022
    Last Verified:
    Jul 1, 2022

    Study Results

    No Results Posted as of Jul 22, 2022