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Enrolling by Invitation

NCT Number: NCT05160688

Changes in Cognition and Psychiatric Disorder Symptoms During Cannabis Abstinence Using a Novel Discordant Twin Design

This study will test whether 42 days of cannabis abstinence, compared to continued cannabis use, is associated with improvements in cognition and psychiatric disorder symptoms. Identical twins, who are concordant on cannabis use, will be experimentally-manipulated to be discordant for 42 days. Each twin, within a twin pair, will be randomly assigned to either the contingency management condition, incentive-based protocol to promote cannabis abstinence, or control condition, no changes in cannabis use requested.

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Key information

Age range

31 year–47 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Jessica M Ross

Aurora, Colorado, 80045, United States

About this study

The proposed project is a randomized controlled trial to compare cognition and psychiatric disorder symptoms between monozygotic (MZ) twin pairs, who are concordant on frequency of cannabis use. Each twin, within the twin pair, will be randomly assigned to either contingency management (CM), monetary incentives provided to reinforce cannabis abstinence, or control, no changes in cannabis use required or reinforced. Participants in the CM condition will receive an increasing schedule of payments at each visit reinforcing continued cannabis abstinence. All participants will receive increases in the payment schedule for attendance of each subsequent assessment. Participants will be assessed on measures of cognition including attention, memory, and processing speed as well as anxiety, depression, and ADHD symptoms. In addition, at each visit participants will complete a qualitative and quantitative drug test. The qualitative drug test will be used to determine if new cannabis use has occurred since the last visit, and will determine if the participant receives payment for abstinence. The investigators will also use previously collected genotype for each participant.

The first aim of this study is to characterize cognitive recovery, across all potential cognitive domains, using an experimental manipulation to achieve discordance between MZ twins on cannabis use. The hypothesis for the first aim is that the abstinent group will have greater improvements in memory and processing speed compared to controls. However, there will not be any group differences between the abstinent group and the control group on attention, language, and executive function performance. The second aim of the proposed project is to characterize psychiatric disorder symptoms by comparing psychiatric disorder symptom changes among the cannabis abstaining twin to their cannabis using co-twin across 42 days. The abstinent group will endorse more psychiatric symptoms during the withdrawal period (up to 14 days) but will endorse fewer psychiatric symptoms at day 28 and 42 compared to the control group. The third aim (exploratory) of the proposed project is to examine how genetic risk for psychiatric disorders interacts with environment (i.e., cannabis abstinence versus continued use) to influence cognitive functioning. The hypothesis for aim 3 is that anxiety, depression, and ADHD polygenic scores will be more strongly associated with cognitive outcomes in the control group compared to the abstinent group.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Monozygotic (MZ) twin pair, in which both twins are willing to participate
  • MZ twin pair must be concordant in their frequency of cannabis use (+/- 2 days)
  • Cannabis use at least 1x per week on most weeks
  • Cannabis use in the past 7 days at the baseline visit
  • Positive qualitative urine toxicology at baseline for THC
  • Located within the state of Colorado

Exclusion criteria

  • Discordance in the twin pairs on a significant, adverse experience, like traumatic brain injury.

Treatment and study plan

Contingency Management

Behavioral

Participants will be paid to abstain from cannabis use.

Primary outcomes

  1. Change in attention performance

    Time frame: Change from baseline to day 42

    Flanker Inhibitory Control and Attention Test on NIH Toolbox: Composite score of accuracy and reaction time

  2. Change in episodic memory

    Time frame: Change from baseline to day 42

    Picture Sequence Memory Test on NIH Toolbox: Cumulative number of correct adjacent pairs

  3. Change in working memory

    Time frame: Change from baseline to day 42

    List Sorting Working Memory Test on NIH Toolbox: Total items correct across all trials

  4. Change in receptive vocabulary

    Time frame: Change from baseline to day 42

    Picture Vocabulary Test on NIH Toolbox: Computer adaptive testing

  5. Change in reading decoding

    Time frame: Change from baseline to day 42

    Oral Reading Recognition Test: Number of letters and words read correctly

  6. Change in immediate memory/verbal learning

    Time frame: Change from baseline to day 4

    Auditory Verbal Learning Test on NIH Toolbox: Total number of words recalled

  7. Change in pattern comparison processing speed

    Time frame: Change from baseline to day 42

    Pattern Comparison Processing Speed Test: Total number of correct responses

  8. Change in oral symbol digit test processing speed

    Time frame: Change from baseline to day 42

    Oral Symbol Digit Test on NIH Toolbox: Total number of correctly identified symbols

  9. Change in attention and executive function

    Time frame: Change from baseline to day 42

    Dimensional Change Card Sort Test on NIH Toolbox: Composite score of accuracy and correct answers

Secondary outcomes

  1. Change in anxiety symptoms

    Time frame: Change from baseline to day 42

    Beck Anxiety Inventory: Total score. Scores range from 0-63 and higher scores indicate higher levels of anxiety.

  2. Change in depressive symptoms

    Time frame: Change from baseline to day 42

    Beck Depression Inventory: Total score. Scores range from 0-63 and higher scores indicate greater levels of depression.

  3. Change in attention deficit/hyperactivity disorder symptoms

    Time frame: Change from baseline to day 42

    Adult Self-Report Scale: Total score. Scores range from 0-72 and higher scores indicate greater level of symptoms of attention deficit/hyperactivity disorder.

Sponsors and collaborators

Lead sponsor

University of Colorado, Denver

Other

Collaborators

  • University of Colorado, Boulder

Registry information

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Dec 16, 2021
Registry last updated
Feb 12, 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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