- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05326685
The Effect of Visual Video With Korotkoff Sounds on Blood Pressure Measurement Skills and Anxiety Levels
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
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Kayseri̇, Turkey, 38000
- Türkan Ülker
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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 |
|---|---|
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Experimental: Intervention
video with korotkoff sounds
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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.
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No Intervention: Control
standart practice
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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.
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pre intervention
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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
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through study completion for each group, an average of 2 hours
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Practice Success
Time Frame: through study completion for each participant, an average of 2 hours
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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
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through study completion for each participant, an average of 2 hours
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: TÜRKAN ÜLKER, TC Erciyes University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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
Studies a U.S. FDA-regulated device product
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