- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05548673
Evaluatıon of the Effıcıency of Stress Management Traınıng Applıed to Nursıng Students (Happy Nursıng Student)
September 19, 2022 updated by: Kamile ÖNER, Ankara Yildirim Beyazıt University
This research was conducted to determine the effect of stress management education on the perceived stress levels, coping styles, self-esteem, happiness and general health of nursing students.
It was conducted in a mixed method as a randomized controlled intervention study.
Study Overview
Detailed Description
The research was carried out at Ankara Yıldırım Beyazıt University in the 2021-2022 academic year.
20 nursing students were assigned to the experimental group and 20 to the control group.
Stress management training was applied to the experimental group selected in the research for eight weeks in 60-90-minute sessions once a week.
No action was taken on the students in the control group.
Quantitative data, Socio-demographic data form, Perceived Stress Scale (PSS), Scale of Stress-Coping Styles (SCSS), Rosenberg Self-Esteem Scale (RSES), Oxford Happiness Scale-Short Form (OHQ-SF) and General Health Questionnaire-12 (GHQ-12).
Qualitative data were collected through a semi-structured focus group interview form with the experimental group after the training.
The analysis of the data was made using the IBM SPSS 25.0 statistical package program.
Study Type
Interventional
Enrollment (Actual)
40
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
-
-
Center
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Ankara, Center, Turkey, 06000
- Ankara Yıldırım Beyazit University
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Having completed the age of 18
- Being a registered (ongoing) Nursing Program student at Ankara Yıldırım Beyazıt University
- Having no problem attending school
- Being open to communication and cooperation
- Not having been diagnosed with any mental illness
- No diagnosis of mental illness in first degree relatives
- Not having a situation that would prevent them from participating in the trainings (Students will be included in the study after being evaluated within the scope of the SCL90-R test results).
Exclusion Criteria:
-
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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group
Stress management training was applied to the experimental group for eight weeks in sessions of 60-90 minutes once a week.
|
The implementation phase is planned for Ankara Yıldırım Beyazıt University (AYBU) Nursing Faculty students.
The stress management training program, which consists of eight sessions, is completed in 8 weeks, once a week.
|
|
No Intervention: Control group.
No action was taken on the students in the control group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quantitative method - The Numerical Rating Scale(NRS)
Time Frame: five months
|
It was applied to the experimental and control groups in order to quantitatively measure the effectiveness of stress management training, which was applied for 8 weeks.
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five months
|
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Qualitative methot-Semi-structured focus group interview form
Time Frame: one weeks
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It was applied to evaluate the opinions and suggestions of the experimental group about the training program.
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one weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived Stress Scale (PSS)
Time Frame: five months
|
The education given was used to determine the perceived stress levels of the students.
While the scores obtained from the PSS range from 0 to 56, a high score from the scale indicates that the person is highly stressed.
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five months
|
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Scale of Stress-Coping Styles (SCSS)
Time Frame: five months
|
The training given was used to determine the students' levels of coping with stress.
Higher scores indicate that the person uses that style more.
The total score is a minimum of 30 and a maximum of 120 points.
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five months
|
|
Rosenberg Self-Esteem Scale (RSES)
Time Frame: five months
|
The education given was used to determine the self-esteem levels of the students.
Scale items score between 0 and 6, and self-esteem; are evaluated as high (0-1 points), medium (2-4 points) and low (5-6 points).
In other words, the higher the score a person gets from the scale, the lower the self-esteem level is.
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five months
|
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Oxford Happiness Scale-Short Form (OHQ-SF)
Time Frame: five months
|
The education given was used to determine the happiness levels of the students.
A score between 7 and 35 is taken from the scale.
A high score from the scale indicates a high level of happiness.
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five months
|
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General Health Questionnaire-12 (GHQ-12)
Time Frame: five months
|
The education given was used to determine the general health levels of the students.
The scale is likert style and consists of 4 options.
The first two options are evaluated as "0" and the last two options as "1" points.
The highest possible score is "12" and the lowest score is "0".
Those who score 4 or more on the scale are evaluated as "high", those with 2-3 points as "medium", and those with less than 2 points as "low".
The higher the score obtained from the scale, the higher the probability of psychiatric disorder.
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five months
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Birgül ÖZKAN, Ankara Yildirim Beyazıt University
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)
July 24, 2020
Primary Completion (Actual)
April 20, 2022
Study Completion (Actual)
September 13, 2022
Study Registration Dates
First Submitted
September 15, 2022
First Submitted That Met QC Criteria
September 19, 2022
First Posted (Actual)
September 21, 2022
Study Record Updates
Last Update Posted (Actual)
September 21, 2022
Last Update Submitted That Met QC Criteria
September 19, 2022
Last Verified
September 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- Ankara Yildirim Beyazıt Univ
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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