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The Effects of Simulation-Based Arterial Blood Pressure Training on Physical Therapy and Rehabilitation Students

NCT07606924 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2026-05-26

No results posted yet for this study

Summary

The aim of this clinical study is to assess the effectiveness of simulation-based arterial blood pressure training provided to undergraduate students in physical therapy and rehabilitation.

The main questions it aims to address are as follows:

\- Does simulation-based arterial blood pressure training affect the knowledge, skills, clinical competence, satisfaction, and self-confidence of undergraduate physical therapy and rehabilitation students? To examine the effects of simulation-based arterial blood pressure training-in which students engage in hands-on practice-on theoretical knowledge, psychomotor skills, practitioner competence, satisfaction, and self-confidence, one control group will participate in the study.

Participants will:

* All participants will receive standard theoretical training on blood pressure measurement and observe a practical demonstration.
* The intervention group will additionally perform blood pressure measurements on a simulator under the supervision of an instructor.
* Assessments will be conducted at the beginning of the study and 21 days later.

Conditions

  • Simulation-based Training

Interventions

OTHER

Simulation-based arterial blood pressure training conducted on an individual basis

After participating in a standard theoretical and practical training session that demonstrated the step-by-step process of measuring arterial blood pressure using a simulator, the participants practiced individually on the simulator under the instructor's supervision.

OTHER

Standard simulation-based arterial blood pressure training

This is a standard theoretical and practical training session that demonstrates the step-by-step process of measuring arterial blood pressure using a simulator.

Sponsors & Collaborators

  • Acibadem University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-06-01
Primary Completion
2026-06-22
Completion
2026-06-22

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07606924 on ClinicalTrials.gov