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

20 mai 2026 mis à jour par: 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.

Aperçu de l'étude

Statut

Complété

Description détaillée

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.

Type d'étude

Interventionnel

Inscription (Réel)

120

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Oui

La 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

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Soins de soutien
  • Répartition: Non randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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.
Aucune 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.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change in Perceived Stress Scale Score
Délai: 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

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Mentorship Evaluation Scale Score
Délai: 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

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Directeur d'études: Seher Yurt, PhD, seher.yurt@kent.edu.tr

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

3 novembre 2025

Achèvement primaire (Réel)

29 décembre 2025

Achèvement de l'étude (Réel)

2 janvier 2026

Dates d'inscription aux études

Première soumission

20 mai 2026

Première soumission répondant aux critères de contrôle qualité

20 mai 2026

Première publication (Réel)

27 mai 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

27 mai 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

20 mai 2026

Dernière vérification

1 mai 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • IKU-NRS-ZA-1

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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