University of Miami
Miami, Florida, 33136, United States
Location status: Recruiting
Location contact
Anjali Sharma, MD
SUB_INVESTIGATOR
Jasmine Agreda, BS
CONTACT
Joanna Starrels, MD
SUB_INVESTIGATOR
Vilma Gabbay, MD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT05453513
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.
Interested in participating?
Request Info18 year–59 year
All sexes
Interventional
Not applicable
Miami, Florida, 33136, United States
Location status: Recruiting
Anjali Sharma, MD
SUB_INVESTIGATOR
Jasmine Agreda, BS
CONTACT
Joanna Starrels, MD
SUB_INVESTIGATOR
Vilma Gabbay, MD
PRINCIPAL_INVESTIGATOR
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Depressed cannabis non-users:
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 However, if SI constitutes an imminent risk to self or others (defined as active SI), the participant will be withdrawn from the study and emergency procedures will be initiated immediately, including ER admission.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:
Non-depressed cannabis users:
Non-depressed cannabis non-users:
fMRI Tasks
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.
Time frame: Up to 12 months
Measures the severity of depressive episodes in patients with mood disorders Scale 0-60 higher more severe
Time frame: Up to 12 months
Self-report measure allowing the assessment of anticipatory and consummatory pleasure 25 to 120 higher more pleasure
Time frame: Baseline
Measured using Magnetic Resonance Imaging. Summary beta values representing the level of brain activity will be calculated.
Time frame: Up to 12 months
Measures cannabis consumption Score range 0 to 185. The higher the score, the greater the usage of cannabis.
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)
Time frame: Up to 12 months
Suggests use of, or exposure to, a product containing THC. pmol/mL
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.
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
Time frame: Up to 12 months
Measures anhedonia, the inability to experience pleasure Score 0-42 greater the score greater the pleasure.
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.
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.
Time frame: up to 12 months
Assesses sleep quality and disturbances over a month period Scores 0-24 higher the score greater sleep dysfunction
Time frame: up to 12 months
Assesses the severity of pain and its impact on functioning. Pain questionnaire (0-10; higher score=worse)
Time frame: up to 12 months
Measures fear and anxiety responses specific to pain Range 0-100 higher the more anxiety symptoms
Time frame: Baseline
HIV RNA test detects HIV and not antibodies 20 to 10,000,000 copies/mL higher the amount the more infectious
Time frame: Up to 12 months
Monitors the immune system Flow cytometry will be used to detect serum CD4, CD8
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
Contact information is provided by the study sponsor or research team.
University of Miami
Other
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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