- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06885489
The Effect of Acceptance and Commitment Therapy-Based Intervention
The Effect of Acceptance and Commitment Therapy-Based Intervention on Depression, Anxiety, Stress and Psychological Well-Being Levels in University Students
Mental health is essential for students' emotional, cognitive, and social well-being. University life presents significant academic, social, and financial challenges, leading to increased stress, anxiety, and depression. These psychological difficulties negatively impact students' academic performance, relationships, and overall quality of life. Despite these challenges, many students avoid seeking professional help.
Acceptance and Commitment Therapy (ACT) is an effective approach that enhances psychological resilience and helps individuals cope with stress, anxiety, and depression. Instead of changing negative thoughts, ACT fosters psychological flexibility, encouraging individuals to develop a healthier relationship with them. Research supports ACT's effectiveness in reducing psychological distress, improving emotional regulation, and enhancing life satisfaction
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ağrı
-
Erzurum, Ağrı, Turkey, 04100
- Atatürk Üniversitesi
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- ust be currently enrolled as a full-time student at a university.
Exclusion Criteria:
- Individuals with significant cognitive impairments or those unable to understand the study procedures.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control Group
No intervention group
|
|
|
Experimental: ACT Intervention Group
The group receiving Acceptance and Commitment Therapy (ACT)-based intervention.
|
This study implements an ACT-based psychological intervention designed to enhance psychological well-being and reduce depression, anxiety, and stress among university students.
The intervention consists of structured sessions focusing on psychological flexibility, mindfulness, acceptance, and value-driven actions.
Participants engage in experiential exercises, cognitive defusion techniques, and behavioral commitment strategies.
The intervention is delivered over 8 weeks, with weekly sessions lasting approximately 40 minutes.
The sessions are conducted in groups by trained professionals.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Depression, Anxiety and Stress Scale (DASS-21)
Time Frame: 8 week
|
DASS-21 is the short version of the Depression, Anxiety and Stress Scale-42 (DASS-42) developed by Lovibond and Lovibond.
The Turkish adaptation of the scale was made by Sarıçam.
The 4-point Likert-type scale includes a total of 21 items consisting of three sub-dimensions: depression, anxiety and stress.
In the normal sample, test-retest reliability coefficients were found to be r=0.68 for depression, r=0.66 for anxiety and r=0.61 for stress.
An individual's score of 5 and above on the depression sub-scale, 4 and above on the anxiety sub-scale and 8 and above on the stress sub-scale is interpreted as indicating the relevant psychological problem.
|
8 week
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- E-95531838-050.99-124695
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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