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

Primary Purpose

Cannabis

Status
Enrolling by invitation
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Contingency management
Sponsored by
University of Colorado, Denver
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Cannabis

Eligibility Criteria

31 Years - 47 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

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

Exclusion Criteria:

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

Sites / Locations

  • Jessica M Ross

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Contingency management

No intervention

Arm Description

Contingency management (CM) is an incentive-based intervention providing patients with tangible rewards as reinforcement for positive behaviors like abstinence from drug use. Incentives are provided with each urine sample that is drug-free and are increased with each subsequent drug-free urine sample. Participants in the CM condition will receive increasing payments for abstinence: $30 on day 3, $45 on day 5, $60 on day 7, $75 on day 14, $90 on day 21, $105 on day 28, and $120 on day 42. Participants in both conditions also receive increasing payment for visit attendance: $10 on day 1, $15 on day 3, $20 on day 5, $25 on day 7, $30 on day 14, $35 on day 21, $45 on day 28, and $55 on day 42. At the end of the baseline visit, participants in the CM condition will sign a behavioral contract with study staff that clearly outlines expectations as well as the payment schedule.

Participants in this condition will be monitored and will not receive any compensation for cannabis abstinence.

Outcomes

Primary Outcome Measures

Change in attention performance
Flanker Inhibitory Control and Attention Test on NIH Toolbox: Composite score of accuracy and reaction time
Change in episodic memory
Picture Sequence Memory Test on NIH Toolbox: Cumulative number of correct adjacent pairs
Change in working memory
List Sorting Working Memory Test on NIH Toolbox: Total items correct across all trials
Change in receptive vocabulary
Picture Vocabulary Test on NIH Toolbox: Computer adaptive testing
Change in reading decoding
Oral Reading Recognition Test: Number of letters and words read correctly
Change in immediate memory/verbal learning
Auditory Verbal Learning Test on NIH Toolbox: Total number of words recalled
Change in pattern comparison processing speed
Pattern Comparison Processing Speed Test: Total number of correct responses
Change in oral symbol digit test processing speed
Oral Symbol Digit Test on NIH Toolbox: Total number of correctly identified symbols
Change in attention and executive function
Dimensional Change Card Sort Test on NIH Toolbox: Composite score of accuracy and correct answers

Secondary Outcome Measures

Change in anxiety symptoms
Beck Anxiety Inventory: Total score. Scores range from 0-63 and higher scores indicate higher levels of anxiety.
Change in depressive symptoms
Beck Depression Inventory: Total score. Scores range from 0-63 and higher scores indicate greater levels of depression.
Change in attention deficit/hyperactivity disorder symptoms
Adult Self-Report Scale: Total score. Scores range from 0-72 and higher scores indicate greater level of symptoms of attention deficit/hyperactivity disorder.

Full Information

First Posted
November 19, 2021
Last Updated
July 17, 2023
Sponsor
University of Colorado, Denver
Collaborators
University of Colorado, Boulder
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1. Study Identification

Unique Protocol Identification Number
NCT05160688
Brief Title
Changes in Cognition and Psychiatric Disorder Symptoms During Cannabis Abstinence Using a Novel Discordant Twin Design
Official Title
Changes in Cognition and Psychiatric Disorder Symptoms During Cannabis Abstinence Using a Novel Discordant Twin Design
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
May 5, 2023 (Actual)
Primary Completion Date
February 1, 2026 (Anticipated)
Study Completion Date
February 1, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Colorado, Denver
Collaborators
University of Colorado, Boulder

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cannabis

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Contingency management
Arm Type
Experimental
Arm Description
Contingency management (CM) is an incentive-based intervention providing patients with tangible rewards as reinforcement for positive behaviors like abstinence from drug use. Incentives are provided with each urine sample that is drug-free and are increased with each subsequent drug-free urine sample. Participants in the CM condition will receive increasing payments for abstinence: $30 on day 3, $45 on day 5, $60 on day 7, $75 on day 14, $90 on day 21, $105 on day 28, and $120 on day 42. Participants in both conditions also receive increasing payment for visit attendance: $10 on day 1, $15 on day 3, $20 on day 5, $25 on day 7, $30 on day 14, $35 on day 21, $45 on day 28, and $55 on day 42. At the end of the baseline visit, participants in the CM condition will sign a behavioral contract with study staff that clearly outlines expectations as well as the payment schedule.
Arm Title
No intervention
Arm Type
No Intervention
Arm Description
Participants in this condition will be monitored and will not receive any compensation for cannabis abstinence.
Intervention Type
Behavioral
Intervention Name(s)
Contingency management
Intervention Description
Participants will be paid to abstain from cannabis use.
Primary Outcome Measure Information:
Title
Change in attention performance
Description
Flanker Inhibitory Control and Attention Test on NIH Toolbox: Composite score of accuracy and reaction time
Time Frame
Change from baseline to day 42
Title
Change in episodic memory
Description
Picture Sequence Memory Test on NIH Toolbox: Cumulative number of correct adjacent pairs
Time Frame
Change from baseline to day 42
Title
Change in working memory
Description
List Sorting Working Memory Test on NIH Toolbox: Total items correct across all trials
Time Frame
Change from baseline to day 42
Title
Change in receptive vocabulary
Description
Picture Vocabulary Test on NIH Toolbox: Computer adaptive testing
Time Frame
Change from baseline to day 42
Title
Change in reading decoding
Description
Oral Reading Recognition Test: Number of letters and words read correctly
Time Frame
Change from baseline to day 42
Title
Change in immediate memory/verbal learning
Description
Auditory Verbal Learning Test on NIH Toolbox: Total number of words recalled
Time Frame
Change from baseline to day 4
Title
Change in pattern comparison processing speed
Description
Pattern Comparison Processing Speed Test: Total number of correct responses
Time Frame
Change from baseline to day 42
Title
Change in oral symbol digit test processing speed
Description
Oral Symbol Digit Test on NIH Toolbox: Total number of correctly identified symbols
Time Frame
Change from baseline to day 42
Title
Change in attention and executive function
Description
Dimensional Change Card Sort Test on NIH Toolbox: Composite score of accuracy and correct answers
Time Frame
Change from baseline to day 42
Secondary Outcome Measure Information:
Title
Change in anxiety symptoms
Description
Beck Anxiety Inventory: Total score. Scores range from 0-63 and higher scores indicate higher levels of anxiety.
Time Frame
Change from baseline to day 42
Title
Change in depressive symptoms
Description
Beck Depression Inventory: Total score. Scores range from 0-63 and higher scores indicate greater levels of depression.
Time Frame
Change from baseline to day 42
Title
Change in attention deficit/hyperactivity disorder symptoms
Description
Adult Self-Report Scale: Total score. Scores range from 0-72 and higher scores indicate greater level of symptoms of attention deficit/hyperactivity disorder.
Time Frame
Change from baseline to day 42

10. Eligibility

Sex
All
Minimum Age & Unit of Time
31 Years
Maximum Age & Unit of Time
47 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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: 1) Discordance in the twin pairs on a significant, adverse experience, like traumatic brain injury.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
J. Megan Ross, Ph.D.
Organizational Affiliation
University of Colorado - Anschutz Medical Campus
Official's Role
Principal Investigator
Facility Information:
Facility Name
Jessica M Ross
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
In accordance with NIH data sharing policies, data produced from this project will be made available to ensure timely translation of research results to improve human health. The investigators believe there is a possibility of deductive disclosure of subjects with unusual characteristics, even though all identifiers would be removed prior to release for sharing. Thus, the investigators will make the data and associated documentation available to users only under a specific data-sharing agreement that requires: (1) a commitment to using the data only for research purposes and not to identify any individual participant; (2) a commitment to securing the data using appropriate computer technology; and (3) a commitment to destroying or returning the data after analyses are completed.

Learn more about this trial

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

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