- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07160153
- Original Trial
Cannabis Abstinence and Neurocognitive Assessment in Adolescence (CANAA)
September 15, 2025 updated by: University Hospital Pilsen
Cannabis Abstinence and Neurocognitive Assessment in Adolescence
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Evaluate the development of cognitive functions following attainment of abstinence in a group of adolescents with cannabis dependence or harmful cannabis use.
Abstinence is confirmed by toxicological testing.
Study Type
Observational
Enrollment (Estimated)
29
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jiri Podlipny, MD, Ph.D.
- Phone Number: +420 377 103 209
- Email: podlipny@fnplzen.cz
Study Contact Backup
- Name: Frantisek Nekvapil, MD
- Phone Number: +420 377 103 101
- Email: nekvapilfr@fnplzen.cz
Study Locations
-
-
Czechia
-
Pilsen, Czechia, Czechia, 30100
- Recruiting
- University Hospital Pilsen
-
Contact:
- Jiri Podlipny, MD, Ph.D.
- Phone Number: +420 377 103 209
- Email: podlipny@fnplzen.cz
-
Contact:
- Frantisek Nekvapil, MD
- Phone Number: +420 377 103 101
- Email: nekvapilfr@fnplzen.cz
-
Principal Investigator:
- Jiri Podlipny, MD, Ph.D.
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Adolescents aged 15-18 years with a diagnosis of cannabis dependence or harmful cannabis use.
Description
Inclusion Criteria:
- Adolescents aged 15-18 years with a diagnosis of cannabis dependence or harmful cannabis use.
Exclusion Criteria:
- psychiatric comorbidity - Dual diagnosis, including psychotic disorders, mood disorders, severe organic brain damage, or autism spectrum disorder, with the exception of compensated and stabilized anxiety disorder. Psychopharmacological treatment is permitted, except for antipsychotics prescribed for psychosis.
- somatic comorbidity - Severe endocrine disorders such as diabetes mellitus, thyroid dysfunction, or severe cardiovascular disease.
- Violation of abstinence between the first and second neuropsychological assessments, as well as severe decompensation of mental state requiring modification of established psychopharmacological treatment.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Group 1
Adolescents aged 15-18 years with a diagnosis of cannabis dependence or harmful cannabis use.
|
Neurocognitive battery: TMT-Trail Making Test Auditory Verbal Learning Test Stroop Test Tower of London (ToL), Shallice version Continuous Performance Test-Identical Pairs Other psychometrics: The level of dependence is quantified using the CAST (Cannabis Abuse Screening Test)
Urine toxicological assessment
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in performance TMT-B
Time Frame: 8 weeks
|
Change in performance on the Trail Making Test - Part B (TMT-B) [Time Frame: after 8 weeks of abstinence from cannabis]
|
8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in performance on AVLT
Time Frame: 8 weeks
|
Change in performance on the Auditory Verbal Learning Test (AVLT) [Time Frame: after 8 weeks of abstinence]
|
8 weeks
|
|
Change in performance on the Stroop Test
Time Frame: 8 weeks
|
Change in performance on the Stroop Test [Time Frame: after 8 weeks of abstinence]
|
8 weeks
|
|
Change in performance on the Tower of London
Time Frame: 8 weeks
|
Change in performance on the Tower of London (Shallice version) [Time Frame: after 8 weeks of abstinence]
|
8 weeks
|
|
Change in performance on CPT-IP
Time Frame: 8 weeks
|
Change in performance on the Continuous Performance Test - Identical Pairs (CPT-IP) [Time Frame: after 8 weeks of abstinence]
|
8 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cannabis Abuse Screening Test versus degree of neurocognitive impairment
Time Frame: 8 weeks
|
Correlation between severity of cannabis dependence (Cannabis Abuse Screening Test, CAST) and degree of neurocognitive impairment [Time Frame: baseline and after 8 weeks of abstinence]
|
8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 3, 2024
Primary Completion (Estimated)
December 31, 2028
Study Completion (Estimated)
August 31, 2029
Study Registration Dates
First Submitted
August 27, 2025
First Submitted That Met QC Criteria
August 27, 2025
First Posted (Estimated)
September 8, 2025
Study Record Updates
Last Update Posted (Estimated)
September 19, 2025
Last Update Submitted That Met QC Criteria
September 15, 2025
Last Verified
August 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CANAA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
Not decided yet because we are still recruiting and waiting for primary outcome.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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