Viewing Study NCT05680649



Ignite Creation Date: 2024-05-06 @ 6:30 PM
Last Modification Date: 2024-10-26 @ 2:49 PM
Study NCT ID: NCT05680649
Status: COMPLETED
Last Update Posted: 2023-01-11
First Post: 2022-12-15

Brief Title: Effect of Breathing Exercise During Peripheral Intravenous Catheter
Sponsor: TC Erciyes University
Organization: TC Erciyes University

Study Overview

Official Title: Effect of Breathing Exercise During Peripheral Intravenous Catheter Implementation on Pain Anxiety and Patient Satisfaction
Status: COMPLETED
Status Verified Date: 2022-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
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 Lb30 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 Lb30 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

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None