NCT05958641

Brief Summary

Based on the biological-psychology-sociological medicine pattern, this study aims to construction an early warning model of the New Psychoactive Substances (NPS) using for adolescents aged 14-35 years old. This study intends to obtain the data related to the behavioral expression of addiction susceptibility genes, adverse childhood experience, cognition, resistance and the use of NPS in adolescents by questionnaire survey (sample size: 200), and then use logistic regression and machine learning to construct an early warning model.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jul 2023

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 16, 2023

Completed
1 day until next milestone

Study Start

First participant enrolled

July 17, 2023

Completed
7 days until next milestone

First Posted

Study publicly available on registry

July 24, 2023

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 31, 2023

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 30, 2023

Completed
Last Updated

July 24, 2023

Status Verified

July 1, 2023

Enrollment Period

4 months

First QC Date

July 16, 2023

Last Update Submit

July 21, 2023

Conditions

Keywords

risk prediction modelNPSaddiction susceptibility genesadverse childhood experienceadolescents

Outcome Measures

Primary Outcomes (9)

  • the cognition of NPS

    knowledge questionnaire of drug types and risk awareness of drug use will be investigated to know the degree of cognition to NPS

    Baseline

  • the resistance of NPS

    the drug refusal self-efficacy scale and the drug use permissive attitude will be used to measure the the resistance of NPS

    Baseline

  • the use of NPS

    there will be some questions to investigate the drug use conditions

    Baseline

  • Adverse Childhood Experience

    the Chinese version of Adverse Childhood Experience Scale with 10 items will be used to measure the adverse childhood experience

    Baseline

  • hedonic hunger

    the Power of Food Scale with 15 items will be used to measure hedonic hunger

    Baseline

  • sensation seeking personality

    the Brief Sensation Seeking Scale for Chinese with 8 items will be used to measure sensation seeking personality

    Baseline

  • prosocial behavior

    the Prosocial Tendencies Measure with 26 items will be used to measure prosocial behavior

    Baseline

  • externalizing behavior

    17 items of aggressive behavior and 15 items of rule-breaking behavior from the Chinese Version of Achenbach Youth Self-Report-2001 Version will be used to measure adolescents' degree of externalizing behavior

    Baseline

  • sleep quality

    the Pittsburgh Sleep Quality Index with 9 items will be used to measure adolescents' sleep quality

    Baseline

Study Arms (1)

Investigation Team

Questionnaires assessed adolescents aged 14-35 years old (including 14,25 years old) who agreed to participate in the study

Other: Questionnaires

Interventions

Participants will be asked to complete the questionnaire including general demographic information, the cognition, resistance and use of NPS as well as the behavioral expression of addiction susceptibility genes and adverse childhood experience.

Investigation Team

Eligibility Criteria

Age14 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodNon-Probability Sample
Study Population

General adolescents between 14-35 years old

You may qualify if:

  • Adolescents aged 14-35 (including 14,35 years old)
  • Agree to participate in the studies

You may not qualify if:

  • Be diagnosed with psychological or mental illness
  • People that are unconscious, emotionally unstable, or unable to communicate normally
  • Patients with severe diseases

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sun Yat-sen University

Guangzhou, Guangdong, 510080, China

Location

MeSH Terms

Conditions

Substance-Related Disorders

Interventions

Surveys and Questionnaires

Condition Hierarchy (Ancestors)

Chemically-Induced DisordersMental Disorders

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Wei Xia, PhD

    Sun Yat-sen University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

July 16, 2023

First Posted

July 24, 2023

Study Start

July 17, 2023

Primary Completion

October 31, 2023

Study Completion

November 30, 2023

Last Updated

July 24, 2023

Record last verified: 2023-07

Data Sharing

IPD Sharing
Will not share

Locations