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Perceived StressNCT07610096

Peer Mentoring and Perceived Stress in First-Year Nursing Students

A study testing Peer Mentor-Mentee Program in people with Perceived Stress and Stress, run by Istanbul Kent University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study aimed to evaluate whether participation in a peer mentor-mentee program was associated with changes in perceived stress among first-year nursing students. Starting university and adapting to nursing education may be stressful for first-year students because of new academic, social, and environmental… Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Perceived Stress, Stress
What is being tested?
Peer Mentor-Mentee Program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
120 participants
Where
1 siteTurkey (Türkiye)
Study dates
3 Nov 2025to 2 Jan 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Istanbul Kent University

    Istanbul

Other trials in Turkey (Türkiye)

About this study

Official title: Changes in Perceived Stress Following a Peer Mentor-Mentee Program Among First-Year Nursing Students: A Controlled Quasi-Experimental Study

This study aimed to evaluate whether participation in a peer mentor-mentee program was associated with changes in perceived stress among first-year nursing students. Starting university and adapting to nursing education may be stressful for first-year students because of new academic, social, and environmental demands. Peer mentoring may support students' adaptation to university life by providing academic, social, and practical support.

This study used a controlled quasi-experimental pretest-posttest design involving first-year nursing students enrolled at the same institution. Students in the intervention group participated in an eight-week peer mentor-mentee program supported by fourth-year nursing students who served as mentors. The program included guidance on adaptation to university life, academic processes, time management, problem-solving, communication, and coping with stress. Students in the control group received the university's routine orientation and standard academic advising services.

Perceived stress was assessed before and immediately after the eight-week intervention using the Perceived Stress Scale. The primary outcome was the change in perceived stress from baseline to post-intervention. Participants in the intervention group also completed the Peer Mentorship Evaluation Scale after the program to evaluate their experience of the mentoring process.

Read the detailed description

This study used a controlled quasi-experimental pretest-posttest design to evaluate changes in perceived stress following a peer mentor-mentee program among first-year nursing students.

The study was conducted with first-year nursing students enrolled in the nursing department at Istanbul Kent University. Students belonged to two pre-existing class sections assigned through the university's administrative student allocation system. To reduce the risk of contamination between intervention and control participants, the two sections were used as the study groups. The sections were allocated by drawing lots, with one section assigned to the intervention group and the other to 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, communication skills, supportive peer relationships, and faculty assessment. 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. During the introductory session, mentors and mentees met face-to-face and were introduced to one another and to the mentoring process. Following the training and matching process, mentors conducted weekly video calls with their assigned mentees via WhatsApp throughout the eight-week program. Mentees could also use their WhatsApp groups to ask questions and seek support from their mentors when needed. When mentors required additional guidance, they could contact a faculty member for support.

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 email when needed.

Data were collected online at two time points: before 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 primary outcome was the change in perceived stress from baseline to post-intervention. The Peer Mentorship Evaluation Scale was administered to intervention participants after the program to evaluate their experience of the mentoring process.

Being tested
Peer Mentor-Mentee Program
Keywords
Peer Mentoring, Nursing Students, Peer Support, Nursing Education, University Adjustment

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Peer Mentor-Mentee ProgramBehavioural

    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. Twelve fourth-year nursing students served as peer mentors, with each mentor matched with five first-year nursing students. Following structured training and face-to-face mentor-mentee matching, mentors conducted weekly video calls with their assigned mentees via WhatsApp throughout the eight-week program. Mentees could also communicate with their mentors through WhatsApp groups to ask questions and seek support when needed. The mentoring process focused on academic guidance, adaptation to university life, time management, and coping with stress. When mentors encountered questions or situations requiring additional guidance, they contacted a faculty member for support.

Study groups in NCT07610096
Study groupRoleWhat they receive
Peer Mentor-Mentee Program GroupExperimentalParticipants 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 on the mentoring process, university adaptation, academic processes, time management, problem-solving, leadership, communication skills, confidentiality, ethical principles, and coping with stress. During the introductory session, mentors and mentees met face-to-face and were introduced to one another and to the mentoring process. Throughout the eight-week program, mentors conducted weekly video calls with their assigned mentees via WhatsApp. Mentees could also use their WhatsApp groups to ask questions and seek support from their mentors when needed.
Receives: Behavioral: Peer Mentor-Mentee Program
Control GroupNo interventionParticipants 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 being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Perceived Stress Scale Score

    Perceived stress was assessed using the Perceived Stress Scale (PSS). 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 was the change in total PSS score from baseline to immediately after completion of the eight-week peer mentor-mentee program.

    Measured: Baseline and immediately after the 8-week intervention

Secondary outcomes (1)
  1. Mentorship Evaluation Scale Score

    The Peer Mentorship Evaluation Scale was administered to participants in the intervention group to evaluate their perceptions of the mentoring experience. 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 favorable evaluation of the mentoring experience.

    Measured: Immediately after the 8-week intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 May 2026
  2. Study start3 Nov 2025
  3. Primary completion29 Dec 2025
  4. Study completion2 Jan 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Non-randomised
Intervention model
Parallel groups
Model description
This is a non-randomized controlled experimental study with a pretest-posttest design. First-year nursing students in one class section were assigned to the intervention group, and students in another class section were assigned to the control group to reduce contamination between groups. The intervention group participated in an eight-week peer mentor-mentee program, while the control group received routine orientation and standard academic advising services.
Masking
None (open label)
Enrolment
120 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07610096
Sponsor's protocol ID
IKU-NRS-ZA-1
Status last verified
Oct 2026
First submitted
20 May 2026
Last updated
26 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Peer Mentor-Mentee Program in people with Perceived Stress and Stress, run by Istanbul Kent University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Perceived Stress Scale Score (time frame: Baseline and immediately after the 8-week intervention). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Oct 2026.

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