- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06464211
The Effect of Family Counseling Program on Anxiety and Conscious Awareness Levels (not)
The Effect of Family Counseling Program Applied to University Students With Future Anxiety on Anxiety and Conscious Awareness Levels
Study Overview
Status
Intervention / Treatment
Detailed Description
This research was conducted as a pre-test, post-test randomized controlled study to determine the effects of a Cognitive Behavioral Therapy (CBT)-based Family Counseling Program on anxiety and mindfulness levels in university students experiencing future anxiety. The study collected data from 20 students, divided equally between 10 participants in the intervention group and 10 in the control group. Data were gathered using a Personal Characteristics Form, the Future Anxiety Scale for University Students, and the Turkish version of the Mindfulness Awareness Scale for Adolescents and Adults.
The intervention group participated in an online CBT-based Family Counseling Program, which was conducted weekly for 8 weeks, each session lasting between 50-60 minutes. For the first 6 weeks, the sessions included only the students, while the last two weeks also involved family members' participation. No intervention was applied to the control group. Both groups were assessed with the aforementioned scales before the intervention and after its conclusion. This study aims to provide insights into the effectiveness of integrating family dynamics into therapeutic practices for reducing anxiety and enhancing mindfulness among students.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Istanbul
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Şişli, Istanbul, Turkey, 34360
- IstanbulUC
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- The level of future anxiety is above 40 points
No problems with speech, perception or hearing
- The person or persons who will be included in the study from family members will be able to participate in the online session at the time required for counseling
- The student will regularly participate in the interview sessions to be held
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: control group
no intervention
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Experimental: experimental group
There were 6 face-to-face sessions with students for 50- 60 minutes/week, and 2 sessions with internet-based video programs with students' families.
Cognitive Behavioral Model-Based Family Counseling Program was conducted.
At least one parent was asked to participate in the family sessions.
After the implementation of the intervention group was completed, the final tests of the scales used in the research were applied again to both the intervention and the control group.
After the data of the study were collected, a focus group interview, one of the interview methods used in qualitative research on the effectiveness and organization of a Cognitive Behavioral Model-Based Family Counseling Program, was conducted for 5 students selected from the initiative group and the effectiveness of the program was evaluated.
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A Cognitive Behavioral Model-Based Family Counseling Program is a therapeutic approach that focuses on identifying and changing negative thought patterns and behaviors within the family unit, using principles of cognitive-behavioral therapy to improve communication, resolve conflicts, and enhance overall family functioning.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Reduction in Future Anxiety Levels
Time Frame: Baseline (at study start) and at 8 weeks post-intervention.
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This measure assesses the change in future anxiety levels among university students participating in the Cognitive Behavioral Therapy-based Family Counseling Program.
The Future Anxiety Scale for University Students will be used to quantify this change.
The scale ranges from a minimum score of 19 to a maximum score of 95.
Higher scores indicate an increase in the level of future anxiety.
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Baseline (at study start) and at 8 weeks post-intervention.
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Improvement in Mindfulness Awareness Levels
Time Frame: Baseline (at study start) and at 8 weeks post-intervention.
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This outcome measures the enhancement in mindfulness awareness levels as determined by the Turkish version of the Mindfulness Awareness Scale for Adolescents and Adults.
Changes from baseline to post-intervention will be assessed to determine the effectiveness of the intervention.
The scale ranges from a minimum score of 18 to a maximum score of 90.
Higher scores indicate an increase in the level of mindfulness awareness
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Baseline (at study start) and at 8 weeks post-intervention.
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Collaborators and Investigators
Investigators
- Principal Investigator: merve geylani, MSc, Istanbul University - Cerrahpasa (IUC)
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
- MGeylani
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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