- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07312591
Using the LINE@ Online Platform to Follow Up on Illegal Drug Use Among College and University Students
December 16, 2025 updated by: Li Yi Xuan, National Taiwan Normal University
Using Line@ Online Platform to Follow up on Counseling Intervention Effectiveness for Illegal Drug Use Among College and University Students
This study developed a LINE@ online platform for tracking college and university students involved in illegal drug use, with the aim of evaluating the effectiveness of the intervention.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Effectiveness indicators were collected using a structured questionnaire, including family functioning, severity of substance dependence, motivation for change, and emotional health management.
In addition, a structured questionnaire was used to gather university students' user evaluations of the LINE@ online platform.
Study Type
Interventional
Enrollment (Estimated)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Li Li, BS
- Phone Number: 0912978806
- Email: bcfs0340090@gmail.com
Study Locations
-
-
Heping E. Rd
-
Taipei, Heping E. Rd, Taiwan, 106
- Recruiting
- National Taiwan Normal University
-
Contact:
- Guo Guo, PhD
- Phone Number: (02)7749-1737
- Email: jonglong@ntnu.edu.tw
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- College students with a history of illegal drug use (confirmed by urine screening or other methods, such as self-reported use, curiosity-driven misuse, or accidental use)
Exclusion Criteria:
- Younger than 18 years old
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control Group
|
|
|
Experimental: LINE@ Online Platform Intervention Group
LINE@ Online Platform Intervention
|
Using digital learning materials covering family functioning, substance dependence severity, motivation for change, and emotional health management.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Family Functioning
Time Frame: To be completed within 2 months from the start of participation
|
1.Assessment of family dynamics and functioning using using validated scales FAMILY APGAR (questionnaire).
2.The score ranges from 0 to 10, with higher scores indicating better family functioning.
|
To be completed within 2 months from the start of participation
|
|
Severity of Substance Dependence
Time Frame: To be completed within 2 months from the start of participation
|
1.Evaluation of the severity of substance dependence among participants using validated scales The Severity of Dependence Scale (questionnaire).
2.The score ranges from 0 to 15, with higher scores indicating a greater level of substance dependence in the participant.
|
To be completed within 2 months from the start of participation
|
|
Motivation for Change
Time Frame: To be completed within 2 months from the start of participation
|
1.Measurement of participants' motivation to change their substance use using validated scales University of Rhode Island Change Assessment (questionnaire).
2.The score ranges from 2 to 10, with higher scores indicating a greater severity of addictive behaviors and a higher level of motivation to change in the participant's clinical course.
|
To be completed within 2 months from the start of participation
|
|
Emotional Health Management
Time Frame: To be completed within 2 months from the start of participation
|
1.Assessment of emotional health management skills through using validated scales Brief Symptom Rating Scale (questionnaire).
2.The score ranges from 0 to 20, with higher scores indicating a greater level of emotional distress.
|
To be completed within 2 months from the start of participation
|
|
Drug Abuse Screening Test
Time Frame: To be completed within 2 months from the start of participation
|
1.Survey on illegal drug use in the past 1 month using validated scales Drug Abuse Screening Test (questionnaire).
2.The score ranges from 0 to 10, with higher scores indicating a higher risk level of illegal drug use.
|
To be completed within 2 months from the start of participation
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
User Evaluation of the LINE@ Online Platform
Time Frame: To be completed within 2 months from the start of participation
|
1.Participants' evaluation of the usability and effectiveness of the LINE@ platform using validated scales System usability scale (questionnaire).
2.The score ranges from 0 to 100, with higher scores indicating a higher evaluation of the educational material by the participants.
|
To be completed within 2 months from the start of participation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 1, 2025
Primary Completion (Estimated)
June 1, 2026
Study Completion (Estimated)
June 1, 2026
Study Registration Dates
First Submitted
September 16, 2025
First Submitted That Met QC Criteria
December 16, 2025
First Posted (Actual)
December 31, 2025
Study Record Updates
Last Update Posted (Actual)
December 31, 2025
Last Update Submitted That Met QC Criteria
December 16, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- 202506HM023
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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