NCT06502314

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
102

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 6, 2024

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 24, 2024

Completed
14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 8, 2024

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

July 8, 2024

Completed
8 days until next milestone

First Posted

Study publicly available on registry

July 16, 2024

Completed
Last Updated

July 16, 2024

Status Verified

July 1, 2024

Enrollment Period

2 months

First QC Date

July 8, 2024

Last Update Submit

July 13, 2024

Conditions

Keywords

Perceived stressstress managementpsychological resiliencehealth studentsmental health

Outcome Measures

Primary Outcomes (3)

  • Change in "Perceived Stress Scale" scores

    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

    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.

  • Change in "Brief Resilience Scale" scores

    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.

Study Arms (2)

intervention group

EXPERIMENTAL

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.

Behavioral: Stress management training

control group

NO INTERVENTION

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.

Interventions

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) .

intervention group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kutahya Health Sciences University

Kütahya, Merkez, 43700, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Psychological Well-Being

Condition Hierarchy (Ancestors)

Personal SatisfactionBehavior

Study Officials

  • Sercan Mansuroğlu, PhD

    Kutahya Health Sciences University

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
FACTORIAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

July 8, 2024

First Posted

July 16, 2024

Study Start

March 6, 2024

Primary Completion

April 24, 2024

Study Completion

May 8, 2024

Last Updated

July 16, 2024

Record last verified: 2024-07

Data Sharing

IPD Sharing
Will not share

Locations