Effect of Peer Mentorship on Stress in First-Year Nursing Students

May 20, 2026 updated by: Istanbul Kent University

The Effect of a Peer Mentor-Mentee Program on Perceived Stress Levels of First-Year Nursing Students: A Controlled Experimental Study

This study aims to evaluate the effect of a peer mentor-mentee program on perceived stress levels among first-year nursing students. Starting university and adapting to nursing education may be stressful for first-year students due to new academic, social, and environmental demands. Peer mentoring may help students adapt to university life, receive academic and social support, and cope more effectively with stress.

This study was designed as a non-randomized controlled experimental study with a pretest-posttest design. The study population consists of first-year nursing students enrolled at the same institution. Students in the experimental group will participate in an eight-week peer mentor-mentee program supported by fourth-year nursing students who serve as mentors. The program includes guidance on adaptation to university life, academic processes, time management, problem-solving, communication, and coping with stress. Mentor-mentee meetings will be conducted face-to-face or online according to student availability. Students in the control group will receive the university's routine orientation and standard academic advising services.

The main hypothesis of the study is that first-year nursing students who participate in the peer mentor-mentee program will have different post-intervention perceived stress levels compared with students in the control group. Perceived stress will be assessed before and after the intervention using the Perceived Stress Scale. The effectiveness of the mentoring process will also be evaluated using the Peer Mentorship Evaluation Scale.

Study Overview

Status

Completed

Detailed Description

This study was designed as a non-randomized controlled experimental study with a pretest-posttest design to evaluate the effect of a peer mentor-mentee program on perceived stress levels among first-year nursing students.

The study was conducted with first-year nursing students enrolled in the nursing department at Istanbul Kent University. To reduce contamination between groups, students from different class sections were assigned to the study groups. One class section formed the intervention group, and another class section formed the control group. The study was completed with 120 students, including 60 students in the intervention group and 60 students in the control group.

The intervention group participated in an eight-week peer mentor-mentee program in addition to the university's routine orientation and standard academic advising services. Twelve fourth-year nursing students served as peer mentors. Mentors were selected based on voluntary participation, academic achievement, effective communication skills, supportive attitudes, and faculty approval. Each mentor was matched with five first-year nursing students.

Before the intervention, mentors and mentees received structured training on the mentoring process, university and department orientation, academic processes, ethical principles, confidentiality, time management, problem-solving, leadership, communication skills, and coping with stress. After the training and matching process, mentor-mentee meetings were conducted face-to-face or online according to student availability. Communication between mentors and mentees was also supported through mobile instant messaging groups.

The control group received the university's routine orientation program and standard academic advising services only. Students in the control group could meet with their academic advisors during advising hours and communicate with them by e-mail when needed.

Data were collected online at two time points: before the implementation of the peer mentor-mentee program and immediately after completion of the eight-week program. Perceived stress was measured using the Perceived Stress Scale. The mentoring process was evaluated using the Peer Mentorship Evaluation Scale. The primary outcome of the study was the change in perceived stress levels from baseline to post-intervention.

Study Type

Interventional

Enrollment (Actual)

120

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

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Being a first-year nursing student at Istanbul Kent University
  • Being enrolled in the nursing department during the study period
  • Being 18 years of age or older
  • Volunteering to participate in the study
  • Providing written informed consent
  • Being able to complete the online data collection forms

Exclusion Criteria:

  • Refusing to participate in the study
  • Not providing informed consent
  • Not completing the pretest or posttest data collection forms
  • Being absent from the peer mentor-mentee program process in a way that prevents participation in the intervention
  • Being a transfer student or previously having completed first-year nursing education

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: Supportive Care
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Peer Mentor-Mentee Program Group
Participants in this arm received an eight-week peer mentor-mentee program in addition to the university's routine orientation and standard academic advising services. First-year nursing students were matched with fourth-year nursing student mentors at a ratio of 1 mentor to 5 mentees. Mentors and mentees received structured training about the mentoring process, university adaptation, academic processes, time management, problem-solving, leadership, communication skills, confidentiality, ethical principles, and coping with stress. Mentor-mentee meetings were conducted face-to-face or online according to student availability, and communication was also supported through mobile instant messaging groups.
The intervention consisted of a structured eight-week peer mentor-mentee program designed to support first-year nursing students during their adaptation to university life and nursing education. Fourth-year nursing students served as peer mentors after receiving training on mentoring roles, communication, confidentiality, ethical principles, time management, problem-solving, leadership, and stress coping. Each mentor was matched with five first-year nursing students. Mentor-mentee meetings were conducted face-to-face or online according to student availability, and communication was supported through mobile instant messaging groups.
No Intervention: Control Group
Participants in this arm received the university's routine orientation program and standard academic advising services only. Students could meet with their academic advisors during advising hours and communicate with them by e-mail when needed. No peer mentor-mentee program was provided to this group during the study period.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Perceived Stress Scale Score
Time Frame: Baseline and immediately after the 8-week intervention
Perceived stress will be assessed using the Perceived Stress Scale. The scale consists of 8 items rated on a 5-point Likert scale from 0 (never) to 4 (very often), with total scores ranging from 0 to 32. Higher total scores indicate higher perceived stress. The primary outcome is the change in perceived stress score from baseline to after completion of the eight-week peer mentor-mentee program.
Baseline and immediately after the 8-week intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mentorship Evaluation Scale Score
Time Frame: Immediately after the 8-week intervention
The effectiveness of the peer mentoring process will be evaluated using the Peer Mentorship Evaluation Scale. The scale consists of 10 items rated on a 7-point Likert scale from 1 (strongly disagree) to 7 (strongly agree), with total scores ranging from 10 to 70. Higher scores indicate a more effective mentoring process.
Immediately after the 8-week intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Seher Yurt, PhD, seher.yurt@kent.edu.tr

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)

November 3, 2025

Primary Completion (Actual)

December 29, 2025

Study Completion (Actual)

January 2, 2026

Study Registration Dates

First Submitted

May 20, 2026

First Submitted That Met QC Criteria

May 20, 2026

First Posted (Actual)

May 27, 2026

Study Record Updates

Last Update Posted (Actual)

May 27, 2026

Last Update Submitted That Met QC Criteria

May 20, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • IKU-NRS-ZA-1

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.

Clinical Trials on Stress

Clinical Trials on Peer Mentor-Mentee Program

Subscribe