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Cannabis Abstinence and Neurocognitive Assessment in Adolescence

Cannabis Abstinence and Neurocognitive Assessment in Adolescence

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07160153
Acronym
CANAA
Enrollment
29
Registered
2025-09-08
Start date
2024-12-03
Completion date
2029-08-31
Last updated
2025-09-19

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

Conditions

Cannabis Dependence, Harmful Use, Cognitive Assessment

Keywords

Cannabis Dependence, Cannabis Use Disorder, Abstinence, Cognitive Function, Disorder; Abstinence; Cognitive Function; Neuropsychological

Brief summary

Cannabis Abstinence and Neurocognitive Assessment in Adolescence

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.

Interventions

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)

DIAGNOSTIC_TESTUrine toxicological assessment

Urine toxicological assessment

Sponsors

University Hospital Pilsen
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to 18 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Change in performance TMT-B8 weeksChange in performance on the Trail Making Test - Part B (TMT-B) \[Time Frame: after 8 weeks of abstinence from cannabis\]

Secondary

MeasureTime frameDescription
Change in performance on AVLT8 weeksChange in performance on the Auditory Verbal Learning Test (AVLT) \[Time Frame: after 8 weeks of abstinence\]
Change in performance on the Stroop Test8 weeksChange in performance on the Stroop Test \[Time Frame: after 8 weeks of abstinence\]
Change in performance on the Tower of London8 weeksChange in performance on the Tower of London (Shallice version) \[Time Frame: after 8 weeks of abstinence\]
Change in performance on CPT-IP8 weeksChange in performance on the Continuous Performance Test - Identical Pairs (CPT-IP) \[Time Frame: after 8 weeks of abstinence\]

Other

MeasureTime frameDescription
Cannabis Abuse Screening Test versus degree of neurocognitive impairment8 weeksCorrelation between severity of cannabis dependence (Cannabis Abuse Screening Test, CAST) and degree of neurocognitive impairment \[Time Frame: baseline and after 8 weeks of abstinence\]

Countries

Czechia

Contacts

Primary ContactJiri Podlipny, MD, Ph.D.
podlipny@fnplzen.cz+420 377 103 209
Backup ContactFrantisek Nekvapil, MD
nekvapilfr@fnplzen.cz+420 377 103 101

Outcome results

None listed

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