- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06701097
Emotion Regulation Training, Nursing Student, and Alexithymia
November 21, 2024 updated by: Günay Öge, Ankara Medipol University
The Effect of Emotion Regulation Training on the Levels of Alexithymia in Nursing College Students
This study aimed to investigate the effects of emotional regulation training, which is a prepared based on the cognitive behavioral approach, on alexithymia in nursing students.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study aimed to reduce alexithymia levels in nursing students with emotion regulation training based on a cognitive behavioral approach.
The study was conducted with 74 nursing students, 37 in the intervention group and 37 in the control group, studying at a foundation university in the 2023-2024 academic year.
The study data were collected using the data collection form and the Toronto Alexithymia Scale-20 (TAS-20).
Data collection tools were applied three times as pre-post and follow-up tests.
Male and female students who met the inclusion criteria of the study were determined by using the pre-test of the population.
For the sample group to represent the population, students with high levels of alexithymia were identified by stratification by determining the class and gender ratios.
Then, students were assigned to intervention and control groups by randomization.
The 7-session training program prepared for the students in the intervention group was applied.
No intervention was made to the control group during the implementation.
After the training sessions were completed, post-test data were collected.
Follow-up measurements were made three months later.
Study Type
Interventional
Enrollment (Actual)
74
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 Locations
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Ankara, Turkey
- Ankara Medipol University
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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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- To be a student of the nursing department
- Agree to participate in the study
Exclusion Criteria:
- Having received psychological support within the last 10 years
- Having a psychiatric disorder
- Not being a citizen of the Republic of Turkey
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: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Emotion regulation training group
Since the number of participants in the intervention group would prevent the training from being given as a group, the participants were divided into three different groups.
Each group was given theoretical training on emotions, thoughts, physical symptoms resulting from emotions, and verbal and non-verbal ways of communicating emotions.
The theoretical training was reinforced with activities such as relaxation exercises, role plays, imagination, brainstorming, etc.
Each training lasted 60-90 minutes.
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Man is a social being and therefore interacts with his environment.
In the process of interaction, they can transfer their feelings, thoughts, and information.
However, the interaction process may not always continue smoothly.
People's inability to express their emotions appropriately today negatively affects communication.
The reason why people cannot express their emotions may be the high level of alexithymia.
The concept of alexithymia means having difficulty in recognizing, expressing, and naming emotions.
High levels of alexithymia in students, who are future healthcare professionals, can negatively affect themselves, other healthcare professionals and the patients they care for; it can cause burnout in healthcare professionals, decrease the quality of care they provide and cause them to experience interpersonal communication conflicts.
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No Intervention: Control group
Participants in the control group did not receive any training.
Only pre-test, post-test, and follow-up tests were applied to the individuals in this group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Toronto Alexithymia-20 Scale
Time Frame: - Before training. -immediately after the training is over. -Three months after training.
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The scale measures the alexithymia level of the individual.
The scale is a Likert-type scale consisting of 20 items and scored between 1-5.
The minimum score that can be obtained from the scale is 20 and the maximum score is 100.
The higher the score obtained from the scale, the higher the alexithymia level of the individual.
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- Before training. -immediately after the training is over. -Three months after training.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
October 2, 2023
Primary Completion (Actual)
December 23, 2023
Study Completion (Actual)
June 28, 2024
Study Registration Dates
First Submitted
November 18, 2024
First Submitted That Met QC Criteria
November 21, 2024
First Posted (Estimated)
November 22, 2024
Study Record Updates
Last Update Posted (Estimated)
November 22, 2024
Last Update Submitted That Met QC Criteria
November 21, 2024
Last Verified
November 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- E.60365
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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