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Impact of Cannabis Use and Abstinence on Emotion

Impact of Cannabis Withdrawal and Early Abstinence on Threat and Reward Processing

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07746440
Acronym
ICAE
Enrollment
30
Registered
2026-08-05
Start date
2022-01-24
Completion date
2024-07-15
Last updated
2026-08-05

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

Conditions

Cannabis Use Disorder, Severe

Brief summary

The goal of this experimental study is to test how three weeks of cannabis abstinence impacts threat and reward processing in females with Cannabis Use Disorder. The main questions it aims to answer are: Compared to using cannabis as usual, will cannabis cue reactivity increase throughout three weeks of abstinence from cannabis? Compared to using cannabis as usual, will threat reactivity be elevated at weeks 1 and 2 of abstinence followed by a decrease at week 3 of abstinence? Compared to using cannabis as usual, will non-drug reward reactivity be lower at weeks 1 and 2 of abstinence followed by an increase at week 3 of abstinence? Compared to successful 3-week abstainers, will threat, non-drug reward, and cannabis cue reactivity differ in relapsers? Researchers will compare females with CUD who abstain from cannabis for three weeks to those who continue to use cannabis as usual to see how cannabis abstinence impacts threat and reward processing. Participants will: Be randomly assigned to continue using cannabis as usual or abstain from cannabis for three weeks Visit the lab 6 times over three weeks, followed by a 1-month follow-up lab visit for the participants assigned to the cannabis abstinence condition Complete phone surveys every other day across the three week study period

Interventions

BEHAVIORALContingency management for cannabis abstinence and lab visit attendance

Escalating monetary reinforcement is provided for continuous cannabis abstinence and lab visit attendance across the three week study period.

BEHAVIORALContingency management for lab visit attendance

Escalating monetary reinforcement is provided for lab visit attendance across the three week study period.

Sponsors

Florida State University
Lead SponsorOTHER
Auburn University
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 30 Years
Healthy volunteers
No

Inclusion criteria

* \>=5 cannabis use days per week on average over the past 3 months * Female * \>=6 past-year CUD symptoms (must include withdrawal and at least one criterion other than craving must be met within the past 3 months) * \>=20 days of cannabis use over the past 30 days * Positive urinalysis for THC * Cannabis is primary substance of abuse

Exclusion criteria

* Current pregnancy * History of psychotic, seizure, or cardiovascular disorder * Immediate plan to quit cannabis * Current treatment for cannabis use * Current daily psychotropic medication use * Lotion allergy * Positive urinalysis for any drug other than THC * CSRSS \>= 4 * Current moderate (4+ criteria) or severe (6+ criteria) substance use disorder (SUD) other than CUD or nicotine dependence * CBD use \>= 9 days

Design outcomes

Primary

MeasureTime frameDescription
Late Positive PotentialBaseline, Week 1, Week 2, Week 3, and (for contingency management abstinence group only) One-Month Follow-UpThe Late Positive Potential (neural measure recorded via electroencephalography) will be quantified from \~400 to 3000ms at central-parietal sensors relative to the onset of a cannabis, neutral, unpleasant, or pleasant image. The Late Positive Potential to cannabis vs. neutral and cannabis vs. pleasant will be the primary contrasts of interest.
Reward PositivityBaseline, Week 1, Week 2, Week 3, and (for contingency management abstinence group only) One-Month Follow-UpThe Reward Positivity (neural measure recorded via electroencephalography) will be quantified from \~200-300ms at frontal-central sensors relative to the onset of monetary win and loss feedback. The win vs. loss contrast will be the primary outcome of interest.
Eyeblink Startle ResponseBaseline, Week 1, Week 2, Week 3, and (for contingency management abstinence group only) One-Month Follow-UpThe Eyeblink Startle Response (recorded via EMG sensors) will be quantified as the peak blink amplitude relative to the onset of an auditory startle probe during blocks with predictable shocks, unpredictable shocks, and no threat of shock. The Eyeblink Startle Response during unpredictable shock threat vs. no shock threat will be the primary contrast of interest.

Secondary

MeasureTime frameDescription
Delta PowerBaseline, Week 1, Week 2, Week 3, and (for contingency management abstinence group only) One-Month Follow-UpDelta Power (neural time-frequency measure recorded via electroencephalography) will be quantified as event-related spectral power from 1-3.5Hz at frontal-central sensors relative to the onset of monetary win and loss feedback. The win vs. loss contrast will be the primary outcome of interest.
Delta Intertrial Phase CoherenceBaseline, Week 1, Week 2, Week 3, and (for contingency management abstinence group only) One-Month Follow-UpDelta Intertrial Phase Coherence (neural time-frequency measure recorded via electroencephalography) will be quantified as intertrial phase coherence of 1-3.5Hz oscillations at frontal-central sensors relative to the onset of monetary win and loss feedback. The win vs. loss contrast will be the primary outcome of interest.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 6, 2026