Cannabis Abstinence and Neurocognitive Assessment in Adolescence
- Conditions
- Cannabis DependenceHarmful UseCognitive 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
- Adolescents aged 15-18 years with a diagnosis of cannabis dependence or harmful cannabis use.
- 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
Name Time Method Change in performance TMT-B 8 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
Name Time Method Change in performance on AVLT 8 weeks Change in performance on the Auditory Verbal Learning Test (AVLT) \[Time Frame: after 8 weeks of abstinence\]
Change in performance on the Stroop Test 8 weeks Change in performance on the Stroop Test \[Time Frame: after 8 weeks of abstinence\]
Change in performance on the Tower of London 8 weeks Change in performance on the Tower of London (Shallice version) \[Time Frame: after 8 weeks of abstinence\]
Change in performance on CPT-IP 8 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, CzechiaJiri Podlipny, MD, Ph.D.Principal InvestigatorFrantisek Nekvapil, MDContact+420 377 103 101nekvapilfr@fnplzen.cz