Effect of Breathing Exercise During Peripheral Intravenous Catheter

Not Applicable

Completed

• Conditions: Venipuncture
• Interventions: Other: Breathing exercise

• Registration Number: NCT05680649
• Lead Sponsor: TC Erciyes University

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.

Study Timeline

• Study Start: 2022-02-24
• Primary Completion: 2022-07-28
• Study Completion: 2022-07-28
• Status Verified: 2022-12
• Study First Submitted: 2022-12-15
• Study First Submitted QC: 2022-12-23
• Last Update Submitted: 2022-12-23
• Study First Posted: 2023-01-11
• Last Update Posted: 2023-01-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 130

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,
• pressure pain threshold mean of 8-16 pounds (Lb), (11) individuals who volunteered to participate in the study.

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,
• in the post-surgical period,
• individuals who did not volunteer to participate in the study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Intervention	Breathing exercise	Breathing exercise

Primary Outcome Measures

Name	Time	Method
Pain level	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	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 Outcome Measures

Name	Time	Method
Satisfaction level	3 minutes after catheter insertion	Satisfaction level measured with Numeric Rating Scale. The number "0" in the scale indicates that the participants are not at all satisfied with the application, and the number "10" indicates the highest level of satisfaction.

Trial Locations

Locations (1)

Erciyes University; 🇹🇷 Kayseri, Turkey