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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04373525
Other study ID # UW 20-189
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date November 1, 2020
Est. completion date August 31, 2025

Study information

Verified date May 2024
Source The University of Hong Kong
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Most of the studies assessing Cannabis Use Disorder (CUD) and neurocognitive functions are cross-sectional without examining the longitudinal changes in neurocognitive function at a within-subject level with respect to the continuum of cannabis use behavior, or mainly studying on the acute cannabis effect. As for the Genome-wide Association studies, the population analyzed for addressing the underlying genetic susceptibility between neurocognitive functions and/or cannabis use or CUD were almost exclusively based on African- or European- American samples or other Caucasian subjects, and thus generalizability to Chinese or to the non-Caucasian population definitely demands more studies. With the upsweeping statistical figures of cannabis use in Hong Kong and Asia, and the substantial falls in the perceived risk and personal disapproval from using cannabis amongst young abusers, coinciding the global advocacy of de-criminalizing cannabis and the increased availability of recreational cannabis worldwide, it is reasonable to predict that there will be a further upsurge in numbers of all aged cannabis users in Hong Kong as in the other part of the world. Therefore, the SToP-C-PeCoG study proposed here as a prospective study in assessing the longer term changes in neurocognitive functions and the associated genetic risks for those repeated and active cannabis users without psychiatric co-morbidity is definitely warranted. The PeCoG study will not only provide the scientific evidence to further unveil the harmful effects on neurocognitive functions for those self-perceived "healthy" users, but also help to raise the public awareness and to improve the understandings to the long-term detrimental effects of cannabis amongst users and non-users. Furthermore, it will provide a chance to study the associated genetic risks for cannabis abusers, in particular in the Asian minority and Chinese, on CUD and poorer neurocognitive outcomes, with genetic vulnerability being generalizable to the local population in Asia. The current study hypothesises that cannabis abusers have neurocognitive function decline over time, and genetic vulnerability is associated with cannabis abusers who have poorer neurocognitive outcomes or with the severity of CUD.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 136
Est. completion date August 31, 2025
Est. primary completion date May 31, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 16 Years to 60 Years
Eligibility Inclusion Criteria: - Age: 16 - 60 years old at the time of enrolment - Able to read and communicate in English and/or Chinese - Able to give informed consent - Using cannabis or marijuana as the primary psychoactive substance of abuse - Repeated and Active cannabis users as defined by Structured Clinical Interview for DSM-5 Disorders Exclusion Criteria: - Age <16 years old - Unable to read English or Chinese - Unable to give informed consent - Had been diagnosed with other Substance Related Disorders, except for Tobacco Use Disorders due to the known frequent comorbid use for cannabis users (12) - Currently taking regular prescribed psychiatric medications, including antipsychotics, antidepressants, mood stabilizers, anti-epileptics, benzodiazepines, hypnotics, and anti-cholinergic medications. - Had been diagnosed with DSM-5 disorders, other than Cannabis Use and related disorders

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Genome analysis
Venous blood will be obtained for later genome analysis

Locations

Country Name City State
Hong Kong Queen Mary Hospital Hong Kong

Sponsors (1)

Lead Sponsor Collaborator
The University of Hong Kong

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type Measure Description Time frame Safety issue
Primary Montreal Cognitive Assessment Subject assessed with a maximum score of 30. Those who score 26 or below will consider to have mild cognitive impairment 18 months
Primary Frontal Assessment Battery Subject who scores 12 or below will be considered having frontal dysexcutive function 18 months
Primary Wechsler Memory Scale Subject will be assessed with the scale for their immediate, delayed, visual and auditory memory 18 months
Primary Genome analysis venous blood test will be done on consented subject for genome analysis for associated single nucleotide polymorphisms on 4 related chromosomes identified from literature associated with cannabis use disorder and neurocognitive impairment Each subject only need to have venous blood test once 1 day within their 18-months study period
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