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Cannabis Abstinence and Neurocognitive Assessment in Adolescence

Recruiting
Conditions
Cannabis Dependence
Harmful Use
Cognitive Assessment
Registration Number
NCT07160153
Lead Sponsor
University Hospital Pilsen
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.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
29
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 & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in performance TMT-B8 weeks

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

Secondary Outcome Measures
NameTimeMethod
Change in performance on AVLT8 weeks

Change in performance on the Auditory Verbal Learning Test (AVLT) \[Time Frame: after 8 weeks of abstinence\]

Change in performance on the Stroop Test8 weeks

Change in performance on the Stroop Test \[Time Frame: after 8 weeks of abstinence\]

Change in performance on the Tower of London8 weeks

Change in performance on the Tower of London (Shallice version) \[Time Frame: after 8 weeks of abstinence\]

Change in performance on CPT-IP8 weeks

Change in performance on the Continuous Performance Test - Identical Pairs (CPT-IP) \[Time Frame: after 8 weeks of abstinence\]

Trial Locations

Locations (1)

University Hospital Pilsen

🇨🇿

Pilsen, Czechia, Czechia

University Hospital Pilsen
🇨🇿Pilsen, Czechia, Czechia
Jiri Podlipny, MD, Ph.D.
Principal Investigator
Frantisek Nekvapil, MD
Contact
+420 377 103 101
nekvapilfr@fnplzen.cz

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