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Stress-Reactivity and Cannabis Use in Cannabis-Using Older Adults

MUSC Specialized Center of Research Excellence (SCORE) on Sex Differences: Stress-Reactivity and Cannabis Use in Cannabis-Using Older Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05072795
Acronym
PUMA
Enrollment
47
Registered
2021-10-11
Start date
2021-11-19
Completion date
2023-06-07
Last updated
2024-08-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cannabis Use

Brief summary

The goal of the study is to evaluate how cannabis use affects memory and thinking skills and response to stress in older adults. The study will also relate cannabis use to Alzheimer's Disease (AD) biomarkers (measurable substances in blood that indicate condition), and test whether sex and hormones play a role in these effects. The study is recruiting adults between the ages of 50 and 80 who use cannabis products on a regular basis. Study participation will last about two weeks.

Interventions

BEHAVIORALTrier Social Stress Task (TSST)

The TSST is a standardized psychological stress challenge which provokes a stress response in a laboratory setting. During the task, saliva samples will be collected for hormone testing along with physiological and subjective measures.

Sponsors

National Institute on Aging (NIA)
CollaboratorNIH
National Institute on Drug Abuse (NIDA)
CollaboratorNIH
Medical University of South Carolina
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age 50-80. * Women must be \>1 year post-menopausal. * English as a first/primary language. * Functional visual and auditory acuity (aided or unaided) to complete tests. * Capacity to independently provide informed consent and function at an intellectual level sufficient to allow completion of all instruments. * Currently meets DSM-5 criteria for CUD or uses cannabis at least 4 days per week * Consent to abstain from alcohol and cannabis use for \>12 hours prior to Study Visit (Day 0), and TSST (Day 8). * Consent to abstain from all drugs other than cannabis or nicotine for the duration of the study.

Exclusion criteria

* Meet DSM-5 criteria for moderate or severe alcohol or substance use disorder (other than nicotine or cannabis) within the last 12 months. * History of major neurocognitive disorder or developmental disorder per DSM-5. * A Telephone Interview for Cognitive Status (TICS) score of less than or equal to 22. * Significant or unstable medical condition/s that impact cognition as deemed by study investigators, such as active significant cardiac, cerebrovascular, neoplastic, infectious, or metabolic disease, or longstanding and intractable severe mental illness (e.g. schizophrenia spectrum disorder, bipolar disorder). * Daily use of medications that adversely impact cognition in aging (i.e. anticholinergics and sedatives). * Current suicidal or homicidal ideation/risk. * Unable to complete/comply with procedures or pose threat to research staff. * Standard MRI contraindications (e.g., implants, claustrophobia). * Women who are pregnant, nursing, or of childbearing potential and not practicing and effective means of birth control.

Design outcomes

Primary

MeasureTime frameDescription
Global Cognitive Ability (GCA)Day 0The primary outcome is the mean Global Cognitive Ability (GCA) z-score, which is a psychometrically robust, factor analytically-derived, demographically-normed index of global cognitive function. A Z-score of 0 represents the population mean with positive scores indicating a higher level of cognitive function and negative scores indicating a lower level of cognitive function than the mean. The investigator will test the hypothesis that women with CUD will have lower GCA scores than men.

Countries

United States

Participant flow

Recruitment details

Participants were recruited between Oct 2021 and May 2023 through community advertisements. The first participant was enrolled on 11/19/2021 and the last participant was enrolled on 5/18/2023.

Pre-assignment details

There was one participant group (N=47). All participants completed cognitive testing on Day 0 and a stress intervention on Day 8. Cognition was assessed independently of the stress intervention and is the primary outcome. N=47 completed the cognition assessments, which we listed as the non-intervention group. Stress intervention was not a primary outcome and is not reported in results section. N=45 completed the Stress Induction and are listed below.

Participants by arm

ArmCount
Stress Induction
Trier Social Stress Task (TSST): The TSST is a standardized psychological stress challenge which provokes a stress response in a laboratory setting. During the task, saliva samples will be collected for hormone testing along with physiological and subjective measures.
47
Total47

Withdrawals & dropouts

PeriodReasonFG000
Overall StudyLost to Follow-up5

Baseline characteristics

CharacteristicStress Induction
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
8 Participants
Age, Categorical
Between 18 and 65 years
39 Participants
Age, Continuous61.11 years
STANDARD_DEVIATION 5.6
Ethnicity (NIH/OMB)
Hispanic or Latino
2 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
45 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
1 Participants
Race (NIH/OMB)
Asian
1 Participants
Race (NIH/OMB)
Black or African American
2 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
1 Participants
Race (NIH/OMB)
White
42 Participants
Region of Enrollment
United States
47 participants
Sex: Female, Male
Female
21 Participants
Sex: Female, Male
Male
26 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 47
other
Total, other adverse events
0 / 47
serious
Total, serious adverse events
0 / 47

Outcome results

Primary

Global Cognitive Ability (GCA)

The primary outcome is the mean Global Cognitive Ability (GCA) z-score, which is a psychometrically robust, factor analytically-derived, demographically-normed index of global cognitive function. A Z-score of 0 represents the population mean with positive scores indicating a higher level of cognitive function and negative scores indicating a lower level of cognitive function than the mean. The investigator will test the hypothesis that women with CUD will have lower GCA scores than men.

Time frame: Day 0

Population: Hypothesis was that women with CUD will have lower GCA scores than men.

ArmMeasureGroupValue (MEAN)Dispersion
Independent of InterventionGlobal Cognitive Ability (GCA)Male-1.99 Standard score (Z-score)Standard Deviation 1.31
Independent of InterventionGlobal Cognitive Ability (GCA)Female-0.82 Standard score (Z-score)Standard Deviation 1.37
p-value: 0.005t-test, 2 sided

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026