The Effect of Visual Video With Korotkoff Sounds on Blood Pressure Measurement Skills and Anxiety Levels

April 8, 2022 updated by: Turkan Ulker, TC Erciyes University

The Effect of Visual Video With Korotkoff Sounds on Blood Pressure Measurement Skills and Anxiety Levels: A Randomized Controlled Study

Background: The aim of this study was to determine the effect of visual video with korotkoff sounds on nursing students' blood presssure measurement skills and anxiety levels.

Methods: This was a randomized controlled experimental study conducted at the nursing department of the faculty of health sciences of a university. Intervention participants were shown and listened visual video with korotkoff sounds before blood presssure measurement. Aural and visual video containing Korotkoff sounds were shown to the students before the practice.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Background: The aim of this study was to determine the effect of visual video with korotkoff sounds on nursing students' blood presssure measurement skills and anxiety levels.

Methods: This was a randomized controlled experimental study conducted at the nursing department of the faculty of health sciences of a university. Intervention participants were shown and listened visual video with korotkoff sounds before blood presssure measurement. Aural and visual video containing Korotkoff sounds were shown to the students before the practice. The data of the research were collected with the State-Trait Anxiety Inventory short version (STAIS-5, STAIT-5) and the Student introduction form.

Study Type

Interventional

Enrollment (Actual)

140

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Kayseri̇, Turkey, 38000
        • Türkan Ülker

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Studying in the first year of the nursing department in the 2021-2022 academic year,
  • Taking the "pulse and blood pressure measurement" course and laboratory practice
  • Students who agree to participate in the study will be included.

Exclusion Criteria:

  • Previous manual blood pressure measurement experience,
  • Those who do not participate in the theoretical part of the "pulse and blood pressure measurement" course,
  • Students who do not attend the lesson on the day of the applications will not be included.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention
video with korotkoff sounds
The State-Trait Anxiety Inventory short version (STAIS-5, STAIT-5) and the student introduction form were applied at the beginning of the study. Then Intervention participants were shown and listened visual video with korotkoff sounds before blood presssure measurement. Afterwards, blood pressure was measured to the students 3 times and 3 measurements were recorded. After the application about 2 hours later, the students State Anxiety Inventory short version (STAIS-5) form was filled again by students.
No Intervention: Control
standart practice

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The State-Trait Anxiety Inventory (STAIS-5, STAIT-5)
Time Frame: pre intervention
State-Trait Anxiety Inventory short version (STAIS-5, STAIT-5)[ Time Frame: pre-intervention ] The STAI consists of two parts; the State Anxiety Inventory (SAI) and the Trait Anxiety Inventory (TAI). The SAI measures anxiety about an event while the TAI measures anxiety level as a personal characteristic. The STAIS-5, STAIT-5 each consists of 5 items. The scale items are scored on a 4-point Likert scale of 0 to 3 (0= Not at all, 1= Somewhat, 2= Moderately so, 3= Very much so). Higher scores indicate greater anxiety. The scale allow researchers to differentiate among anxious and healthy participants.
pre intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
State Anxiety Inventory (STAIS-5)
Time Frame: through study completion for each group, an average of 2 hours
The SAI items are scored on scored on a 4-point Likert scale of 0 to 3 (0= Not at all, 1= Somewhat, 2= Moderately so, 3= Very much so). Higher scores indicate greater anxiety
through study completion for each group, an average of 2 hours
Practice Success
Time Frame: through study completion for each participant, an average of 2 hours
blood pressure was measured to all students 3 times and all measurements were recorded. the instructors informed students about BPM and then paired them up, who then took each other's blood pressure using a sphygmomanometer and a stethoscope with headphones that enable both the participant and the instructors to listen to Korotkoff sounds. The instructors evaluated the participants'BPM performanceby listening to the Korotkoff sounds by one of the headphones and by monitoring the manometer
through study completion for each participant, an average of 2 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: TÜRKAN ÜLKER, TC Erciyes University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 3, 2022

Primary Completion (Actual)

March 11, 2022

Study Completion (Actual)

March 27, 2022

Study Registration Dates

First Submitted

April 1, 2022

First Submitted That Met QC Criteria

April 8, 2022

First Posted (Actual)

April 13, 2022

Study Record Updates

Last Update Posted (Actual)

April 13, 2022

Last Update Submitted That Met QC Criteria

April 8, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 31 (Other Identifier: IASO Thessalias)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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