NCT06827418

Brief Summary

The aim of this study is to determine the effect of simulation and peer teaching methods on nursing students' ability to assess blood pressure. The study population will consist of first-year nursing students. All students will complete the "Demographic Characteristics Form" and the "Blood Pressure Knowledge Test" (pre-test). Students will be randomized according to their average scores, and three groups will be formed. Experimental Group 1 Students will practice the psychomotor steps of blood pressure measurement through peer teaching. Experimental Group 2 students will practice the psychomotor steps of blood pressure measurement using a simulator. Control group students will practice the psychomotor steps of blood pressure measurement through traditional laboratory training, which is instructor-centered. They will practice blood pressure measurement steps on low-fidelity mannequins and on each other. After completing the two-session psychomotor skills training, all students will be assessed using the "VAS" to determine their confidence and anxiety levels. One week after the training, all students will measure the blood pressure of a healthy adult in the skills laboratory. During the measurement, the researcher will evaluate the students using the "Blood Pressure Measurement Checklist." After the procedure, the students will complete the "Blood Pressure Knowledge Test" (post-test) and the "VAS" to assess their confidence and anxiety levels. Four to six weeks after the training, all students will measure the blood pressure of a hospitalized adult patient in a clinical setting. Following the procedure, students will complete the "Blood Pressure Knowledge Test" (floow up test) and the "VAS" (third measurement) to assess their confidence and anxiety levels.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
93

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2025

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

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 3, 2025

Completed
11 days until next milestone

First Posted

Study publicly available on registry

February 14, 2025

Completed
17 days until next milestone

Study Start

First participant enrolled

March 3, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 20, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 20, 2025

Completed
Last Updated

June 11, 2025

Status Verified

February 1, 2025

Enrollment Period

3 months

First QC Date

February 3, 2025

Last Update Submit

June 10, 2025

Conditions

Outcome Measures

Primary Outcomes (3)

  • Cognitive knowledge related to blood pressure

    The Blood Pressure Knowledge Test will be used for assessment. It was developed by Takmak and Kurban (2018) and consists of 20 multiple-choice questions, each with five options. Each question has only one correct answer.

    from enrollment to the end of the 6-week follow-up period.

  • blood pressure psychomotor measurement skill

    The Blood Pressure Measurement Checklist will be used for assessment. It consists of procedural steps that thoroughly evaluate the process of blood pressure measurement and assessment. To ensure an objective evaluation of students, it has been designed as a rubric-based scoring tool. The checklist is categorized as follows: \*\*"Correct" (2 points), "Incorrect/Incomplete" (1 point), and "Not Observed" (0 points).\*\*

    from the teaching methods are applied to the end of the 6-week follow-up period

  • confidence and anxiety levels

    The Visual Analog Scale (VAS) will be used for assessment. It is a single-item measurement tool that allows participants to mark their subjective state on a visual scale, providing a simple and quick application. The scale is typically a 100 mm horizontal line, on which participants indicate their perceived level. As the score increases, confidence level and anxiety level also increase.\*\*

    from the teaching methods are applied to the end of the 6-week follow-up period

Study Arms (3)

Peer teaching

EXPERIMENTAL

Experimental Group 1 (Peer Teaching): Students will practice the psychomotor steps of blood pressure measurement through peer teaching. Third- and fourth-year nursing students will serve as peer educators. Students will apply the skill steps under the guidance of an upper-class peer instructor.

simulation

EXPERIMENTAL

Experimental Group 2 (Simulation): Students will practice the psychomotor steps of blood pressure measurement using a simulator.

Other: simulation

control group

NO INTERVENTION

Control Group (Traditional Laboratory Training): Students will practice the psychomotor steps of blood pressure measurement through traditional laboratory training, which is instructor-centered. They will practice blood pressure measurement steps on low-fidelity mannequins and on each other.

Interventions

Students will practice the psychomotor steps of blood pressure measurement using a simulator.

simulation

Students will practice the psychomotor steps of blood pressure measurement through peer teaching. Third- and fourth-year nursing students will serve as peer educators. Students will apply the skill steps under the guidance of an upper-class peer instructor.

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • First-time enrollment in the Fundamentals of Nursing course
  • Willingness to participate in the study

You may not qualify if:

  • Having a high school, associate degree, or bachelor's degree in a health-related field
  • Having previously taken a course on blood pressure measurement
  • Having a hearing impairment
  • The student choosing to withdraw from the study at any stage
  • Failure to complete the data collection forms

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gazi University

Ankara, Turkey (Türkiye)

Location

Study Officials

  • Evrim Sarıtaş

    doctor research assistant

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
FACTORIAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Gazi University Faculty of Nursing, doctoral assistant professor

Study Record Dates

First Submitted

February 3, 2025

First Posted

February 14, 2025

Study Start

March 3, 2025

Primary Completion

May 20, 2025

Study Completion

May 20, 2025

Last Updated

June 11, 2025

Record last verified: 2025-02

Data Sharing

IPD Sharing
Will not share

Locations