Standardized Patients in Arterial Pressure Monitoring Training

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20+
SponsorYuzuncu Yil University

About this trial

This study aims to evaluate and compare the effects of using standardized patients versus static manikins in nursing education for arterial blood pressure monitoring and stabilization training. The primary objective is to investigate the impact of these two different simulation methods on students' cognitive load, clinical skills, and self-efficacy levels.

Arterial pressure monitoring is a critical, invasive intervention commonly performed in intensive care units and operating rooms, requiring a high degree of precision. While traditional technical skill assessments usually focus solely on procedural success scores or completion speed, this study utilizes the framework of Cognitive Load Theory to examine the mental toll (intrinsic, extrinsic, and germane load) and psychological readiness (self-efficacy) experienced by nursing students during the procedure.

The study will be conducted as a randomized controlled experimental trial with 3rd-year nursing students who have successfully completed their Medical-Surgical Nursing course. Participants will be randomly assigned to either the experimental group or the control group:

The Experimental Group will receive theoretical and practical training, followed by performing the arterial pressure monitoring line stabilization on a "Standardized Patient" (an experienced healthcare professional acting a scenario with a moving limb to mimic real clinical chaos without any actual invasive intervention).

The Control Group will receive the same training but will perform the stabilization procedure on a traditional static medical manikin.

Data will be collected using a Descriptive Information and Performance Recording Form (to measure procedural time and error rates), the Cognitive Load Scale, and the Self-Efficacy Scale for Clinical Skills. Measurements will be taken at baseline (pre-test) and immediately after the intervention (post-test). The findings of this study are expected to provide evidence-based guidance for developing "mind-friendly" nursing curricula and safer, more realistic simulation protocols that enhance student self-efficacy while ensuring patient safety before entering actual clinical environments.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Being a undergraduate nursing student currently enrolled in the specified nursing department/faculty.

Volunteering to participate in the study and providing written informed consent.

Taking the relevant clinical nursing course for the first time.

Having successfully completed the baseline theoretical lectures related to vital signs and basic invasive procedures.

Disqualifiers

Having prior formal clinical experience or advanced training regarding invasive arterial blood pressure monitoring or line stabilization.

Having a known physical or visual impairment that would prevent the participant from performing psychomotor simulation tasks.

Repeating the academic year or the clinical course due to prior failure. --Withdrawing from the study voluntarily or failing to attend the mandatory 45-minute baseline theoretical training session.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Arterial Pressure Monitoring Training

    Behavioral

    This behavioural intervention consists of an advanced simulation session following standard theoretical and practical training.

Treatment groups

74 Participants
are divided into 2 treatment groups
Group A: Standardized Patient GroupExperimental treatment 1 intervention
Group B: Static Manikin GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Cognitive Load Level

Assessed using a standardized Cognitive Load Scale (or Cognitive Load Questionnaire). This scale measures the mental effort and cognitive burden experienced by students during the arterial pressure monitoring stabilization procedure. The total score ranges from a minimum score to a maximum score \[10 to 100\]. Higher scores indicate a higher level of cognitive load and mental fatigue during the clinical task.

Time frame
Within the same day, immediately after the completion of the simulation procedure (Day 1)
2

Clinical Self-Efficacy Level

Assessed using a standardized Clinical Self-Efficacy Scale to measure nursing students' self-confidence and perceived competence regarding invasive arterial blood pressure monitoring and line stabilization. The total score ranges from a minimum score to a maximum score \[5 to 25\]. Higher scores indicate greater self-efficacy and clinical confidence.

Time frame
Within the same day, immediately after the completion of the simulation procedure (Day 1).

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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