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

20 de maio de 2026 atualizado por: 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.

Visão geral do estudo

Status

Concluído

Descrição detalhada

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.

Tipo de estudo

Intervencional

Inscrição (Real)

120

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Sim

Descrição

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

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Cuidados de suporte
  • Alocação: Não randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
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.
Sem intervenção: 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.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Change in Perceived Stress Scale Score
Prazo: 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

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Mentorship Evaluation Scale Score
Prazo: 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

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Diretor de estudo: Seher Yurt, PhD, seher.yurt@kent.edu.tr

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

3 de novembro de 2025

Conclusão Primária (Real)

29 de dezembro de 2025

Conclusão do estudo (Real)

2 de janeiro de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

20 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

20 de maio de 2026

Primeira postagem (Real)

27 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

27 de maio de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

20 de maio de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • IKU-NRS-ZA-1

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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