The Effectiveness of Local Dry Cold, Hot and Vibration Applications in Peripheral Intravenous Catheterization

Not Applicable

Completed

• Conditions: Pain Management; Nausea; Vomiting; Emergency Unit; Diarrhea

• Registration Number: NCT06378424
• Lead Sponsor: Uludag University

Brief Summary

Aim: The aim of the present study was to examine the effect on venous dilation, procedure duration and pain severity of local hot, cold and vibration applications performed on the intervention area before peripheral intravenous catheterization in adults.

Methods: The study included 120 adults who were randomly selected between March and August 2023. One application group (n=30) received local hot application, one group (n=30) received local cold application, and one (n=30) received local vibration using the Buzzy® device. The applications, to the site of the peripheral intravenous catheterization, lasted one minute. The control group (n=30) the received standard peripheral intravenous catheterization application. The groups' venous dilation was assessed on the vein assessment scale and the level of pain felt during catheterization was assessed using a visual analog scale.

Detailed Description

Not available

Study Timeline

• Study Start: 2023-03-22
• Primary Completion: 2023-03-22
• Study Completion: 2023-08-23
• Status Verified: 2024-04
• Study First Submitted: 2024-04-18
• Study First Submitted QC: 2024-04-18
• Last Update Submitted: 2024-04-18
• Study First Posted: 2024-04-22
• Last Update Posted: 2024-04-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

• Being in accordance with time and place
• Being aged between 18 and 65 years
• Being able to evaluate the visual analog scale correctly
• Participating voluntarily in the research.

Exclusion Criteria

• Not participating voluntarily in the research
• Not fitting the inclusion criteria of the research
• Having a vision or hearing problem
• Having a mastectomy
• Having any illness which could affect pain perception, such as sensory-motor disorder, diabetes, peripheral vascular diseases or peripheral neuropathy
• Having an allergy to heat and cold application
• Having phlebitis, scar tissue, dermatitis, an incision or findings of infection at the place where the intervention was to be performed
• Having taken an analgesic (within the previous six hours) or an anesthetic agent before the peripheral intravenous catheterization procedure

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
venous dilation in score	6 months	Vein Assessment Scale was used in the study to evaluate individuals' veins. There are five assessment steps: (1) veins are neither visible nor palpable, (2) veins are visible but not palpable, (3) veins are barely visible and palpable, (4) veins are visible and palpable, and (5) veins are clearly visible and easily palpable.
procedure duration in sec	6 months	In the stages of the peripheral intravenous catheterization intervention of individuals in the application and control groups, a chronometer was started immediately after an automatic tourniquet was attached to the patient's arm. After catheterization was completed successfully and before the evaluation material was applied, the chronometer was stopped, and the procedure duration was recorded in the form of seconds on the data collection form.
pain intensity in mm	6 months	A 10-cm vertical VAS was used to evaluate the severity of pain felt by the individuals during the procedure. One end indicated lack of pain and the other the most severe pain possible. Pain severity was evaluated in millimeters.

Secondary Outcome Measures

Name	Time	Method
height	6 months	height in meters
weight	6 months	weight in kilograms

Trial Locations

Locations (1)

Bursa Uludag University Hospital; 🇹🇷 Bursa, Nilüfer, Turkey