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NCT Number: NCT05453513

The Neural Underpinnings of Depression and Cannabis Use in Young People Living With HIV

To elucidate mechanisms of substance use disorders (SUD) and comorbid mental illnesses in people living with HIV (PLWH), the study team seeks to investigate reward and pain circuitry in cannabis use and depression comorbidity, two highly prevalent conditions in PLWH. The study team proposes a tightly integrative study to test the overall hypothesis that cannabis use and depression in young PLWH have an additive effect, inducing both reward deficits and pain hypersensitivity, and that this pattern will predict worse outcomes at 1 year follow-up.

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Key information

Age range

18 year–59 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Miami

Miami, Florida, 33136, United States

Location status: Recruiting

Location contact

Anjali Sharma, MD

SUB_INVESTIGATOR

Jasmine Agreda, BS

CONTACT

[email protected]

305-243-5510

Joanna Starrels, MD

SUB_INVESTIGATOR

Vilma Gabbay, MD

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • HIV seropositivity confirmed with lab report, medical records, or HIV testing.
  • Between the ages of 18-39 years
  • Fluency in English or Spanish
  • Ability to provide informed consent and perform study procedures, including estimated full-scale intelligence quotient (IQ) >75 to ensure that participants are able to understand the study.
  • Cannabis users: To capture a wide range of cannabis use frequency, meeting Diagnostic and Statistical Manual 5 (DSM-5) criteria for Cannabis use Disorder (CUD) will not be required. However, in order to ensure sufficient exposure, cannabis use will be significant (self-reported use on ≥20 of the prior 30 days and positive THC urine toxicology).
  • Depressed: In order to capture a wide range of depression illness severity, we will allow participants with subthreshold depression, defined as a raw severity score of ≥12 on the Montgomery Asberg Depression Rating Scale (MADRS).

Exclusion criteria

  • Perinatally acquired HIV infection, as early neurodevelopmental alterations and HIV legacy effects may exist in this group
  • Pregnancy or lactation
  • Current Substance Use Disorder other than cannabis or nicotine
  • Certified for or self-reported medical cannabis use, or intent to become certified
  • Current cocaine use by self-report or urine toxicology
  • central nervous system (CNS) disease or injury, or neuro-degenerative disease
  • Unique pain syndromes (e.g. multiple sclerosis, rheumatoid arthritis);
  • Severe medical illness such as end-stage renal disease, heart failure, cirrhosis, or cancer
  • MRI contraindication such as claustrophobia, metallic ink tattoos, or pacemaker.

Depressed cannabis non-users:

  • At baseline, all participants will be psychotropic-medication-free for ≥1 month prior to study enrollment (or ≥3 months for medications with longer half-lives). Benzodiazepines and sleeping aids taken on an as-needed basis will be allowed, however we will require a 4-day abstinence period before the scan.
  • Exclusionary are participants with a DSM-5 diagnoses of bipolar disorder, psychotic disorders, autism spectrum disorders, and all non-cannabis substance-related disorders will be exclusionary. disorder (PTSD) are not uncommon among depressed individuals and will be
  • Anxiety disorders, obsessive-compulsive disorder (OCD), and post-traumatic stress are allowed as long as depressive symptoms are primary.

atypical of depression. • Suicidal ideations (SI) without a specific plan (defined as passive SI) are common in depression and will be allowed. However, if SI constitutes an imminent risk to self or others (defined as active SI), the participant will be withdrawn from the study and emergency procedures will be initiated immediately, including ER admission.

Depressed cannabis users:

  • Exclusion criteria will be the same as depressed cannabis non-users except for cannabis use.

Non-depressed cannabis users:

  • Will have no major psychiatric conditions other than cannabis use/disorder.

Non-depressed cannabis non-users:

  • Exclusion criteria will be the same as for non-depressed cannabis users; in addition participants will not report cannabis use in the prior 90 days and have a urine toxicology test negative for cannabis.

Treatment and study plan

MRI Study

Behavioral

fMRI Tasks

Primary outcomes

  1. Addiction Severity Index (ASI)

    Time frame: Up to 1 year

    The number of days using illicit opioids in the past 30 days per self-report as collected through the Addiction Severity Index.

  2. Montgomery Asberg Depression Rating Scale (MADRS) Scale

    Time frame: Up to 12 months

    Measures the severity of depressive episodes in patients with mood disorders Scale 0-60 higher more severe

  3. Temporal Experience of Pleasure Scale (TEPS)

    Time frame: Up to 12 months

    Self-report measure allowing the assessment of anticipatory and consummatory pleasure 25 to 120 higher more pleasure

  4. Neural Circuitry measured by MRI

    Time frame: Baseline

    Measured using Magnetic Resonance Imaging. Summary beta values representing the level of brain activity will be calculated.

Secondary outcomes

  1. Daily Sessions Frequency Age Quantity of Cannabis Use Inventory (DFAQ- CU)

    Time frame: Up to 12 months

    Measures cannabis consumption Score range 0 to 185. The higher the score, the greater the usage of cannabis.

  2. Timeline Followback (TLFB)

    Time frame: Up to 12 months

    Tool to obtain a variety of estimates of marijuana, cigarette, and other drug use. scores range from days of use (0-30)

  3. tetrahydrocannabinol (THC) Metabolite, Serum

    Time frame: Up to 12 months

    Suggests use of, or exposure to, a product containing THC. pmol/mL

  4. Fagerström Test for Nicotine Dependence full-term normal delivery (FTND)

    Time frame: Up to 12 months

    The FTND is a validated, 6-item self-report instrument that evaluates the intensity of physical addiction to nicotine. Three items are rated yes/no (0/1), and the other three items are rated on a scale from 0-3. Items are summed to yield a total score of 0-10, with higher scores reflecting greater nicotine dependence.

  5. Beck Depression Inventory-II (BDI-II)

    Time frame: Up to 12 months

    Designed to assess the presence and severity of depressive symptoms Score 0-63 higher the score greater the depression

  6. Snaith-Hamilton Pleasure Scale (SHAPS)

    Time frame: Up to 12 months

    Measures anhedonia, the inability to experience pleasure Score 0-42 greater the score greater the pleasure.

  7. Alcohol Use Disorders Identification Test-Consumption (AUDIT-C)

    Time frame: Up to 12 months

    Alcohol consumption will be measured using total score on the 3-item Alcohol Use Disorders Identification Test-Consumption (AUDIT-C) which includes typical quantity and frequency, and frequency of binge drinking (# of drinks modified by age based on the NIAAA Youth Guide). Higher score indicates worse outcomes.

  8. Cannabis Use Problem Identification Test (CUPIT)

    Time frame: Up to 12 months

    6-item self-reported questionnaire assessing cannabis use and dependence; Range 3-82, higher values indicating a more severe cannabis use disorder.

  9. Pittsburgh sleep quality index

    Time frame: up to 12 months

    Assesses sleep quality and disturbances over a month period Scores 0-24 higher the score greater sleep dysfunction

  10. Brief Pain Inventory (BPI)

    Time frame: up to 12 months

    Assesses the severity of pain and its impact on functioning. Pain questionnaire (0-10; higher score=worse)

  11. Pain Anxiety Symptom Scale (PASS-20)

    Time frame: up to 12 months

    Measures fear and anxiety responses specific to pain Range 0-100 higher the more anxiety symptoms

  12. HIV RNA test

    Time frame: Baseline

    HIV RNA test detects HIV and not antibodies 20 to 10,000,000 copies/mL higher the amount the more infectious

  13. cluster of differentiation 4 (CD4+) / cluster of differentiation 8 (CD8+)

    Time frame: Up to 12 months

    Monitors the immune system Flow cytometry will be used to detect serum CD4, CD8

  14. HIV Visual Analogue Scale (HIV-VAS)

    Time frame: 12 month

    The VAS asks individuals to mark a line at the point along a continuum showing how much of each drug they have taken in the last 4 weeks 0-30 higher score worse pain

Study contacts

Contact information is provided by the study sponsor or research team.

Vilma Gabbay, MD

CONTACT

[email protected]

305-243-2382

Sponsors and collaborators

Lead sponsor

University of Miami

Other

Collaborators

  • National Institute on Drug Abuse (NIDA)

Registry information

Important dates

Study start
2022
Primary completion
2027
Study completion
2027
First posted
Jul 12, 2022
Registry last updated
Jun 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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