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NCT06714578

Construction of a Risk Screening Tool for New Psychoactive Substance Misuse Among Adolescents and Young Adults

Not yet recruiting Last updated 18 December 2024
What this trial tests

trial testing Questionnaire and Physical Exam in Drug Misuse in 1,035 participants. Not yet recruiting.

Timeline
15 December 2024
Primary endpoint
15 August 2025
1 December 2025

Quick facts

Lead sponsorWei XIA, PhD
StatusNot yet recruiting
Study typeOBSERVATIONAL
Enrollment1,035
Start date15 December 2024
Primary completion15 August 2025
Estimated completion1 December 2025
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Wei XIA, PhD

Who can join

Adults 14 to 35, any sex, with Drug Misuse or Addiction. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this observational study is to construct a risk tool available for screening young adults and adolescents at high risk of drug misuse and provides a chance for early intervention to young adults and adolescents at high risk of drug misuse, which prevent the onset and development of drug addiction in the future.The main question it aims to answer is: 1. Explore the occurrence and influencing factors of new psychoactive substance misuse among young adults and adolescents; 2. Construct a risk prediction model for new psychoactive substance misuse among young adults and adolescents and conduct internal verification of the model; 3. Based on the results of the prediction model, select the optimal model to initially form a concise scale "Screening Tool for the Risk of New Psychoactive Substance Misuse among Young Adults and Adolescents"; 4. Conduct external verification of the tool, and revise and improve the screening tool, form the final version of the screening tool, and verify the application performance of the screening tool.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Questionnaire and Physical Exam

Trials testing the same drug.

Other Wei XIA, PhD trials

Trials by the same sponsor.

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