- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06502314
The Effectiveness of Stress Management Training on Perceiving and Coping With Stress and Developing Resilience
The Effectiveness of Stress Management Training Given to First-class Health Students in Perceiving and Coping With Stress and Developing Resilience: A Randomized Controlled Trial
Associate degree students studying in the field of health perform their professions in the status of intermediate staff related to health in our country. They are in direct or indirect contact with every segment of the society within the health system. They are also in a multidisciplinary team. This enables them to interact within the team. Therefore, it can be clearly said that the stress they will be in may affect other team members. In previous studies in the literature, it is seen that more studies have been conducted with undergraduate health professional candidates. However, considering that associate degree health students start their professional life at a younger age, it can be thought that they may have more difficulties in coping with the stress that the health sector may cause. This situation can be facilitated by strengthening their psychological resilience. In this study, it can be said that it is important to provide stress management training and measure its effectiveness by taking these factors into consideration. It can be thought that the results will contribute to the importance by filling the gap in the literature.
Objective: This study was a pretest-posttest randomised controlled psychoeducational intervention in which the effect of stress management training given to first-year health students on their perceived stress, coping methods and psychological resilience was examined.
Research hypotheses H1: Perceived stress post-test scores of first-year health students who received stress management training will be lower than those who did not receive the same training.
H2: The post-test scores of the first-year health students who received stress management training will be higher than the post-test scores of the students who did not receive the same training.
H3: First-year health students who receive stress management training will have higher psychological resilience post-test scores than students who do not receive the same training.
Methods: The study was conducted with 102 health students, 51 intervention and 51 control. Randomly assigned intervention group received stress management training consisting of 7 modules for 7 weeks. No intervention was given to the control group. Data were collected using sociodemographic form, perceived stress scale, stress coping methods scale and short psychological resilience scale. Pre-test and post-tests were administered to both groups.
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Merkez
-
Kütahya, Merkez, Turkey, 43700
- Kütahya Health Sciences University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- First-year associate degree health students who voluntarily accepted to participate in the study,
- Who were 18 years of age or older,
- Who were continuing their active education.
Exclusion Criteria:
- First-year associate degree health students who voluntarily not accepted to participate in the study,
- Who were under 18 years of age,
- Who were not continuing their active education.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: intervention group
In the first interview with the students assigned to the intervention group, students were informed about the purpose of the study and the process, and pre-tests were applied to the students after their consent was obtained.
After 1 week, students randomly assigned to the intervention group were given psychoeducation on stress management consisting of 7 modules each lasting 120 minutes (with a break), on a day determined during the week for 7 weeks.
Two weeks after the training was completed, post-tests were applied to the intervention group students.
|
It is a psychoeducational program that includes seven modules (1. Stress and its components, 2. Stress Management, 3. Crisis and its components, 4. Crisis Management, 5. Anger and its components, 6. Anger Management, 7. Psychological resilience) . |
|
No Intervention: control group
In the first interview with the students assigned to the control group, students were informed about the purpose of the study and the process, and pre-tests were applied to the students after their consent was obtained.
Ten weeks after, post-tests were applied to the control group students.
During this process, no intervention was applied to the control group.
After the study was completed, the same stress management training was given to the control group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in "Perceived Stress Scale" scores
Time Frame: It was applied as a pre-test before the intervention and as a post-test 2 weeks after the intervention completed, within 1 week, and the change was observed.
|
This scale evaluates the stress perceptions of individuals in the face of certain situations encountered in their lives.
The scale has a five-point Likert scale.
The scale has two sub-dimensions but the total scale score was used for this study.
The lowest score that can be obtained from the scale is 0 and the highest score is 56.
The higher the score obtained by the individuals from the scale, the higher the stress perception.
It was aimed to compare and evaluate the change in perceived stress levels of the participants before and after the planned psychoeducation for 7 weeks.
|
It was applied as a pre-test before the intervention and as a post-test 2 weeks after the intervention completed, within 1 week, and the change was observed.
|
|
Change in "Stress Coping Methods Scale" scores
Time Frame: It was applied as a pre-test before the intervention and as a post-test 2 weeks after the intervention completed, within 1 week, and the change was observed.
|
The coping methods scale was used to measure coping methods with stress.
The scale consists of a five-factor structure but the total scale score was used for this study.
Consisting of 24 statements, the scale is graded in 5-point Likert type.
It can be said that individuals develop methods of coping with stress as the score they get from the scale increases.
It was aimed to compare and evaluate the changes in the participants' methods of coping with stress before and after the psychoeducation planned for 7 weeks.
|
It was applied as a pre-test before the intervention and as a post-test 2 weeks after the intervention completed, within 1 week, and the change was observed.
|
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Change in "Brief Resilience Scale" scores
Time Frame: It was applied as a pre-test before the intervention and as a post-test 2 weeks after the intervention completed, within 1 week, and the change was observed.
|
The scale is a 5-point Likert-type, 6-item, self-report measurement tool developed in order to measure the psychological resilience of individuals.
High scores indicate high psychological resilience.
It was aimed to compare and evaluate the changes in the participants' psychological resilience before and after the psychoeducation planned for 7 weeks.
|
It was applied as a pre-test before the intervention and as a post-test 2 weeks after the intervention completed, within 1 week, and the change was observed.
|
Collaborators and Investigators
Investigators
- Study Director: Sercan Mansuroğlu, PhD, Kütahya Health Sciences University
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
Other Study ID Numbers
- KHSU-MANSUROGLU-001
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
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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