Viewing Study NCT06563648



Ignite Creation Date: 2024-10-26 @ 3:38 PM
Last Modification Date: 2024-10-26 @ 3:38 PM
Study NCT ID: NCT06563648
Status: COMPLETED
Last Update Posted: None
First Post: 2024-08-12

Brief Title: The Effect of Local Cold Application and ShotBlocker Use in Subcutaneous Injection on Injection Pain and Patient Satisfaction
Sponsor: None
Organization: None

Study Overview

Official Title: The Effect of Local Cold Application and ShotBlocker Use in Subcutaneous Injection on Injection Pain and Patient Satisfaction
Status: COMPLETED
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The research was conducted as a single-blind randomized controlled experimental study to determine the effect of ShotBlocker and local cold application on pain and patient satisfaction in subcutaneous heparin injection
Detailed Description: The research was conducted as a single-blind randomized controlled experimental study to determine the effect of ShotBlocker and local cold application on pain and patient satisfaction in subcutaneous heparin injection The research was conducted with 208 patients hospitalized in the Cardiology and Internal Medicine clinics at Izmir Atatürk Training and Research Hospital between April 2022 and April 2024 Patients were assigned to four groups ShotBlocker n52 ShotBlocker placebo n52 local cold application n52 and control n52 groups using the randomization algorithm

A ShotBlocker was placed on the arm of the patients in the ShotBlocker group during the injection and the injection was performed from the part where the opening was located by lightly pressing with the fingertips throughout the injection During the injection the back side of the ShotBlocker was placed on the arm of the patients in the ShotBlocker placebo group and the injection was performed by gently pressing with the fingertips throughout the injection Local cold application was applied to the arm of the patients in the local cold application group for five minutes using a cold pack and then the injection was performed Patients in the control group were injected with a routine subcutaneous injection procedure In all groups the injection took 30 seconds and was performed by researcher At the first minute after the injection the patients were evaluated about the pain they felt during the injection and their satisfaction with the injection by a different reseacher Data were collected by face-to-face interview technique using an informed consent form individual identification form visual analog scale and visual patient satisfaction scale Ethics committee permission institutional permission and written permission from the patients were obtained for the implementation of the research Number percentage median mean and standard deviation Mann Whitney U test Kolmogorov-Smirnov test Kruskal Wallis H test Bonferroni and chi-square test were used in the analysis of the data

Study Oversight

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