Ignite Creation Date:
2024-06-16 @ 11:51 AM
Last Modification Date:
2024-10-26 @ 3:31 PM
Study NCT ID:
NCT06443099
Status:
COMPLETED
Last Update Posted:
2024-06-07
First Post:
2024-05-29
Brief Title:
Needle and Shotblocker on Pain and Satisfaction in Intramuscular Injection Pain
Sponsor:
Necmettin Erbakan University
Organization:
Necmettin Erbakan University
Study Overview
Official Title:
The Effect of Cold Needle and Shotblocker on Pain and Satisfaction in Intramuscular Injection Pain A Randomized Controlled Trial
Status:
COMPLETED
Status Verified Date:
2024-10
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:
In this study it is aimed to compare cold needle and shotblocker in intramuscular injection pain This is a triple-blind randomized clinical trial June September 2024 the universe of the research will be composed of patients who applied to the emergency department of Necmettin Erbakan University Faculty of Medicine Hospital for cyanocobalamin injection Considering that losses may occur during the data collection process the study will be completed with a total of 120 patients Intramuscular injection of the deltoid November will be applied to the intervention-1 group with a cold needle intervention-2 group with a shotblocker and the control group with the standard method People will be determined by block randomization After each application the pain and satisfaction due to the injection will be evaluated The data will be compared between the groups
Detailed Description:
This study aims to compare cold injection and ShotBlocker in intramuscular injection pain This is a triple-blind randomized clinical trial The population of the research will consist of patients who applied to the emergency department of Necmettin Erbakan University Faculty of Medicine Hospital to receive cyanocobalamin injection between June and September 2024 Considering that losses may occur during the data collection process the study will be completed with a total of 120 patients The data of the study will be collected with the Patient Diagnosis Form Visual Analog Scale VAS and Injection Satisfaction Scale Block randomization method will be used to assign participants to groups All injections will be performed by a single nurse working in the injection unit in accordance with the research procedure Once the injection procedure is completed participants will be asked to rate injection pain and satisfaction Pain assessment will be performed by another emergency nurse who is independent from the study and contributes to the study Researchers will participate in this process as observers The people who will perform the application and evaluate the pain and satisfaction will be different In this way the person evaluating the pain will not know which application was performed on the participant and blinding will be ensured Additionally the data of the study will be coded as A B and C and entered into SPSS thus ensuring statistical blinding Thus it is planned to conduct the research with triple blinding All injections will be made using cyanocobalamin injection 1 ml 5 cc syringe 25 Gauge orange syringe tip Before the injection it will be checked whether the pain score is 0 with VAS The participant will be given a Fowler position the deltoid area will be checked on the arm to be treated the arm will be flexed and brought closer to the body and the position will be given Injections will be given to each group according to the IM injection application protocol Intramuscular injection will be applied to the deltoid muscle in the intervention-1 group with a cold needle in the intervention-2 group with a shot blocker and in the control group with the standard method Subjects will be determined by block randomization All participants will be allowed to rest for two minutes after each injection After two minutes they will be asked to mark the level of pain caused by the procedure on the VAS Similarly they will be asked to mark their satisfaction with the procedure on the injection satisfaction scale Then the line marked by the person will be measured with a 10 cm ruler and the numerical equivalent of pain and satisfaction will be determined Data will be compared between groups
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