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Clinical Trials/NCT05680649
NCT05680649
Completed
Not Applicable

Effect of Breathing Exercise During Peripheral Intravenous Catheter Implementation on Pain, Anxiety, and Patient Satisfaction

TC Erciyes University1 site in 1 country130 target enrollmentFebruary 24, 2022
ConditionsVenipuncture

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Venipuncture
Sponsor
TC Erciyes University
Enrollment
130
Locations
1
Primary Endpoint
Pain level
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

This study was carried out to determine the effect of breathing exercise performed during peripheral intravenous catheter (PIVC) application on pain, anxiety and patient satisfaction.

The study was completed as a randomized controlled experimental study with a total of 130 individuals who met the inclusion criteria. The Descriptive Characteristics Questionnaire, the State-Trait Anxiety Inventory, and the Numerical Rating Scale were used to collect the data of the study. In addition, Algometer (66 Lb/30 Kg) device was used to evaluate the pain pressure threshold in determining the individuals to be included in the research sample. The individuals in the intervention group were given diaphragmatic breathing exercise while applying the catheter, and the individuals in the control group were inserted without any application.

Detailed Description

This study was carried out to determine the effect of breathing exercise performed during peripheral intravenous catheter (PIVC) application on pain, anxiety and patient satisfaction. The study was completed as a randomized controlled experimental study with a total of 130 individuals who met the inclusion criteria, 65 of whom were in the intervention group and 65 in the control group. Ethics committee approval, institutional permission, and written informed consent from individuals were obtained in the study. The Descriptive Characteristics Questionnaire, the State-Trait Anxiety Inventory, and the Numerical Rating Scale were used to collect the data of the study. In addition, Algometer (66 Lb/30 Kg) device was used to evaluate the pain pressure threshold in determining the individuals to be included in the research sample. The individuals in the intervention group were given diaphragmatic breathing exercise while applying the catheter, and the individuals in the control group were inserted without any application.

Registry
clinicaltrials.gov
Start Date
February 24, 2022
End Date
July 28, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sevda Korkut

Instructor

TC Erciyes University

Eligibility Criteria

Inclusion Criteria

  • able to speak and understand Turkish,
  • between the ages of 18-65,
  • having orientation to place and time,
  • without any psychiatric disease and hearing problems,
  • not using central nervous system drugs,
  • people who having PIVC indication,
  • no analgesic or anesthetic agent was applied 24 hours before PIVC application,
  • not have any pain in any part of the body that may affect the results of the study,
  • no PIVC experience in the last month,
  • 20-G catheter will be applied,

Exclusion Criteria

  • Infection in the area where PIVC will be applied, -having previous operation, scarring, psoriasis, active dermatitis in the area - -
  • where PIVC will be applied,
  • with peripheral nerve disease,
  • no catheter applied to the forearm veins,
  • having diabetes,
  • with peripheral neuropathy,
  • diagnosed with cancer,
  • receiving cancer treatment,
  • with respiratory disease,
  • who have an obstacle to breathing exercise,

Outcomes

Primary Outcomes

Pain level

Time Frame: 3 minutes after catheter insertion

Pain level measured with Numeric Rating Scale. The number "0" on the scale means that they do not feel any pain and the number "10" refers to the worst pain.

Anxiety level

Time Frame: 3 minutes after catheter insertion

Anxiety level measured with Numeric Rating Scale. The number "0" on the scale means that they do not feel any anxiety and the number "10" refers to the highest level of anxiety.

Secondary Outcomes

  • Satisfaction level(3 minutes after catheter insertion)

Study Sites (1)

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