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CompletedNCT07884422Updated Oct 20, 2026

Cognitive Behavioral Therapy for Substance Use and Mental Health in University Students

An interventional study of Cognitive-Behavioral Therapy (CBT)-Based Group Intervention and Group Counseling Program in Substance Use Behavior, sponsored by Mehmet Akif Ersoy University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-20.

Sponsored by Mehmet Akif Ersoy University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 9 months after the study started (first participant enrolled Jan 2026, registered Oct 2026).
Updated Oct 20, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

This study examined changes in substance use frequency, psychological well-being, and psychological symptoms among university students participating in a cognitive-behavioral therapy (CBT)-based group intervention.

A total of 90 university students participated in a three-group, non-randomized, quasi-experimental study. Participants were allocated according to their availability for scheduled sessions. The CBT group included 34 students who participated in seven weekly sessions lasting approximately 90 minutes each. The inactive control group included 33 students who received no intervention. The active comparison group included 23 students who participated in seven group counseling sessions focusing on personal development, communication, time management, motivation, and study skills.

Participants completed measures of substance use frequency, psychological well-being, and psychological symptoms before the intervention, after the intervention, and at a three-month follow-up.

The study aimed to compare changes in these outcomes across the three groups. Because group allocation was not randomized, the findings cannot establish that the intervention caused the observed changes.

Read the detailed description

This study used a three-group quasi-experimental design with pretest, posttest, and three-month follow-up assessments to examine substance use frequency, psychological well-being, and psychological symptoms among university students.

Participants were recruited through university announcements and posters. Ninety volunteers participated in the study. Allocation to the three conditions was based on participants' availability for scheduled sessions rather than random assignment.

The CBT intervention group (n = 34) participated in seven weekly group sessions, each lasting approximately 90 minutes. The sessions addressed group orientation and an introduction to CBT in the context of substance use; relationships among situations, emotions, perceptions, and behaviors; cross-sectional case formulation; automatic thoughts, cognitive distortions, and cognitive restructuring; behavioral techniques and coping skills; problem-solving and life skills; and consolidation of gains and relapse prevention.

The inactive control group (n = 33) received no intervention during the study period.

The active comparison group (n = 23) participated in seven group counseling sessions addressing personal development, communication, time management, motivation, and study skills. Both active programs were facilitated by the principal investigator.

Data were collected at baseline, immediately after the intervention period, and approximately three months after completion of the intervention. Substance use frequency was assessed using three self-report items concerning tobacco or nicotine use, heavy episodic alcohol consumption, and nonmedical prescription medication use during the preceding 12 months. Psychological well-being and psychological symptoms were assessed using self-report measures.

The study was conducted without random assignment. Consequently, potential selection bias and differences between the groups must be considered when interpreting the findings.

02

Conditions studied

  • Substance Use Behavior

Keywords

  • Cognitive Behavioral Therapy
  • University Students
  • Substance Use
  • Psychological Well-Being
  • Psychological Symptoms
  • Group Counseling
03

In context

Substance-Related Disorders

2,181 studies on the registry are indexed under Substance-Related Disorders; 399 are open to participants now.

This study's enrollment of 90 is below the median of 108 across 1,770 interventional studies indexed under Substance-Related Disorders.

Browse Substance-Related Disorders studies →

Lead sponsor

Mehmet Akif Ersoy University is the lead sponsor of 25 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Being a university student aged 18 years or older.
  • Voluntarily agreeing to participate in the study.
  • Providing written informed consent.
  • Being available to participate in the scheduled study activities and assessments.

Exclusion criteria

Exclusion Criteria:

  • Being unable to attend the scheduled group sessions because of timetable conflicts, employment, or health-related circumstances.
  • Declining or withdrawing voluntary participation.
  • Being unwilling to participate in a group-based intervention.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
90 participants (actual)

Study arms

  • Experimental
    CBT-Based Intervention Group

    The experimental group consisted of 34 university students who received a seven-session cognitive-behavioral therapy (CBT)-based group intervention. Sessions were conducted once weekly and lasted approximately 90 minutes each. The program addressed CBT principles related to substance use, relationships among situations, emotions, perceptions, and behaviors, cognitive restructuring, behavioral coping strategies, problem-solving skills, and relapse prevention. The intervention was delivered by the principal investigator.

    Behavioral: Cognitive-Behavioral Therapy (CBT)-Based Group Intervention

  • No intervention
    No-Intervention Control Group

    The no-intervention control group consisted of 33 university students who did not receive a structured psychological intervention during the study period. Participants completed the same outcome assessments as the other groups at baseline, posttest, and three-month follow-up.

  • Active comparator
    Group Counseling Comparison Group

    The active comparison group consisted of 23 university students who participated in seven group counseling sessions focusing on personal development, communication skills, time management, motivation, and study skills. The sessions were facilitated by the principal investigator. Participants completed outcome assessments at baseline, posttest, and three-month follow-up.

    Behavioral: Group Counseling Program

Interventions

  • BehavioralCognitive-Behavioral Therapy (CBT)-Based Group Intervention

    The intervention consisted of seven weekly group sessions, each lasting approximately 90 minutes. The program addressed cognitive-behavioral principles related to substance use, relationships among situations, emotions, perceptions, and behaviors, cognitive restructuring, behavioral coping strategies, problem-solving skills, and relapse prevention. The sessions were delivered by the principal investigator.

  • BehavioralGroup Counseling Program

    The intervention consisted of seven group counseling sessions focusing on personal development, communication skills, time management, motivation, and study skills. The sessions were facilitated by the principal investigator.

06

What researchers measure

Primary outcomes

  1. Substance Use Frequency

    The outcome was assessed using a three-item self-report substance use frequency questionnaire measuring the frequency of tobacco/nicotine use, heavy episodic alcohol consumption, and nonmedical prescription medication use during the past 12 months. Each item was scored from 1 (never) to 5 (daily), yielding a total score ranging from 3 to 15. Higher scores indicate more frequent substance use.

    Time frame: Baseline, immediately after the 7-week intervention, and 3-month follow-up.

Secondary outcomes

  1. Psychological Well-Being

    Psychological well-being was assessed using a 12-item self-report measure covering hedonic and eudaimonic dimensions of well-being. Higher scores indicate greater psychological well-being. Hedonic and eudaimonic scores were analyzed separately.

    Time frame: Baseline, immediately after the 7-week intervention, and 3-month follow-up.

  2. Psychological Symptoms

    Psychological symptoms were assessed using an 18-item self-report symptom inventory covering somatization, depression, and anxiety. Higher scores indicate greater symptom severity. The three symptom dimensions were analyzed separately.

    Time frame: Baseline, immediately after the 7-week intervention, and 3-month follow-up.

07

Study locations

1 site
  • Burdur Mehmet Akif Ersoy University
    Burdur, Burdur 15030, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No — Individual participant data will not be publicly shared because the dataset contains sensitive information about substance use and psychological symptoms, and there is no established plan for sharing participant-level data.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 20, 2026
Show all 1 update
  1. Oct 20, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07884422
Lead sponsor
Mehmet Akif Ersoy University
Responsible party
Hakan ACAR (Lecturer, Mehmet Akif Ersoy University) — Principal investigator
First posted
Oct 20, 2026
Start date
Jan 12, 2026
Primary completion
Jun 5, 2026
Completion
Jun 5, 2026
Last update
Oct 20, 2026

Study contacts

Hakan ACAR, PhD
principal investigator · Burdur Mehmet Akif Ersoy University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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