CHAMPS: Cannabis, HIV and Mental Processing Systems

Sponsor
Washington University School of Medicine (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05430490
Collaborator
Temple University (Other)
320
2
39.3
160
4.1

Study Details

Study Description

Brief Summary

This study employs novel methods to identify key determinants and consequences of concurrent HIV infection and regular cannabis use. This study will acquire extensive phenotype data from peripheral and brain markers of immune activation, brain structure, and neuropsychological performance (NP) in persons living with HIV (PLWH) receiving combination anti-retroviral therapy (cART) (80 regular cannabis users and 80 non-users) and HIV uninfected (HIV-) controls (80 regular cannabis users and 80 non-users). This study will provide key insights into the effects of regular cannabis and HIV on peripheral and brain markers of immune function and NP in PLWH and HIV- controls. These insights are critical for cure strategies and ongoing HIV treatment initiatives.

Condition or Disease Intervention/Treatment Phase
  • Procedure: MRI
  • Other: NeuroPsychological Testing
  • Procedure: Blood Draw
  • Other: Questionnaires
  • Procedure: Lumbar Puncture

Study Design

Study Type:
Observational
Anticipated Enrollment :
320 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
Cannabis, HIV and Mental Processing Systems
Actual Study Start Date :
Mar 23, 2022
Anticipated Primary Completion Date :
Jun 30, 2025
Anticipated Study Completion Date :
Jun 30, 2025

Arms and Interventions

Arm Intervention/Treatment
HIV+ Cannabis User

Persons diagnosed with HIV who identify as using medical or recreational marijuana

Procedure: MRI
Multimodal neuroimaging on 3T Prisma Fit MRI

Other: NeuroPsychological Testing
A series of written, verbal, and motor tasks requiring the participant to follow instructions, remember words and numbers, draw objects, and complete timed actions.

Procedure: Blood Draw
Laboratory reports (CMP, CBC, Lipids)

Other: Questionnaires
Life history, current behaviors, and substance use surveys

Procedure: Lumbar Puncture
Optional procedure which involves obtaining cerebral spinal fluid through a needle in the lower back

HIV+ Cannabis Non-User

Persons diagnosed with HIV who identify as not using medical or recreational marijuana

Procedure: MRI
Multimodal neuroimaging on 3T Prisma Fit MRI

Other: NeuroPsychological Testing
A series of written, verbal, and motor tasks requiring the participant to follow instructions, remember words and numbers, draw objects, and complete timed actions.

Procedure: Blood Draw
Laboratory reports (CMP, CBC, Lipids)

Other: Questionnaires
Life history, current behaviors, and substance use surveys

Procedure: Lumbar Puncture
Optional procedure which involves obtaining cerebral spinal fluid through a needle in the lower back

HIV- Cannabis User

Persons without HIV who identify as using medical or recreational marijuana

Procedure: MRI
Multimodal neuroimaging on 3T Prisma Fit MRI

Other: NeuroPsychological Testing
A series of written, verbal, and motor tasks requiring the participant to follow instructions, remember words and numbers, draw objects, and complete timed actions.

Procedure: Blood Draw
Laboratory reports (CMP, CBC, Lipids)

Other: Questionnaires
Life history, current behaviors, and substance use surveys

Procedure: Lumbar Puncture
Optional procedure which involves obtaining cerebral spinal fluid through a needle in the lower back

HIV- Cannabis Non-User

Persons without HIV who identify as not using medical or recreational marijuana

Procedure: MRI
Multimodal neuroimaging on 3T Prisma Fit MRI

Other: NeuroPsychological Testing
A series of written, verbal, and motor tasks requiring the participant to follow instructions, remember words and numbers, draw objects, and complete timed actions.

Procedure: Blood Draw
Laboratory reports (CMP, CBC, Lipids)

Other: Questionnaires
Life history, current behaviors, and substance use surveys

Procedure: Lumbar Puncture
Optional procedure which involves obtaining cerebral spinal fluid through a needle in the lower back

Outcome Measures

Primary Outcome Measures

  1. Effect of cannabis use on peripheral and brain immune activation and inflammation in virally controlled PLWH on cART. [Years 1-5]

    Validated plasma and cerebrospinal fluid (CSF) markers of immune health and inflammation (e.g., CD14, CD16, Neopterin, etc.), as well as novel neuroimaging methods of neuro-inflammation (e.g., DTI & DBSI, 3T MRI) will be used to evaluate brain inflammation.

Secondary Outcome Measures

  1. Effect of cannabis use on cognitive performance and brain structure in both PLWH/CB+ and CON/CB+. [Years 1-5]

    Neuropsychological assessment results will be normed and converted into Z scores for comparison with brain volumes calculated from the 3T.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Participants must be 18-70 years old.

  2. PLWH must have documented HIV infection for approximately 1 year, be on a cART regimen for approximately ≥3 months, and be virally well-controlled (< 200 copies/mL).

  3. HIV- controls must have confirmed HIV- serostatus.

  4. Participants must complete at least 9 years of education.

  5. Participants must be able to provide informed consent.

  6. Female participants must have a negative pregnancy test or written documentation of tubal ligation, hysterectomy, post-menopausal status, etc. and cannot be breastfeeding.

  7. Participants should have no contraindications to an MRI scan.

  8. Participants should be willing to have cannabis use history confirmed via clinical interview and urine analysis .

  9. All inclusion criteria at PI discretion.

Exclusion Criteria:
  1. History of neurological disorder (e.g., stroke, head injury with loss of consciousness for >5 minutes, developmental learning disability, etc.).

  2. Uncontrolled major affective disorder; history of bipolar disorder or schizophrenia. Major depression controlled with no hospitalizations or suicidal ideation in the past year is allowed.

  3. Current substance use disorder (SUD) as defined by DSM-5 criteria besides cannabis use disorder (CUD) (though a past SUD > 1 year before the time of study enrolment will be allowed).

  4. currently prescribed anti-coagulants (only exclusionary if participant will engage in optional LP).

  5. an allergy to lidocaine or similar anesthetic (only exclusionary if participant will engage in optional LP).

  6. a history of a bleeding disorder (only exclusionary if participant will engage in optional LP).

  7. claustrophobia or a pacemaker that would prevent magnetic resonance imaging (MRI) scanning.

  8. all exclusion criteria at PI discretion.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Washington University School of Medicine Saint Louis Missouri United States 63110
2 Temple University Lewis Katz School of Medicine Philadelphia Pennsylvania United States 19140

Sponsors and Collaborators

  • Washington University School of Medicine
  • Temple University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Washington University School of Medicine
ClinicalTrials.gov Identifier:
NCT05430490
Other Study ID Numbers:
  • 202107149
First Posted:
Jun 24, 2022
Last Update Posted:
Jun 24, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 24, 2022