Testing Different Methods of Intramuscular Injection

NCT05577832 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2024-03-25

No results posted yet for this study

Summary

The goal of this clinical trial is to compare in different injection techniques. The main question\[s\] it aims to answer are:

* Is there a difference between the pain levels due to needle insertion in the injection made with the HST Technique, the ShotBlocker technique and the standard technique?
* Is there a difference between the hematoma levels of the injection made with the HST Technique, the ShotBlocker technique and the standard technique?
* Is there a difference between the comfort levels of the injection made with the HST Technique, ShotBlocker technique and standard technique?
* Is there a difference between the satisfaction levels of the patients with the injection made with the HST Technique, ShotBlocker technique and standard technique?
* Is there a difference between the injection fear levels of patients with HST Technique, ShotBlocker technique and standard technique?

Conditions

  • Injection Fear
  • Injection Site Bruising
  • Pain, Acute
  • Satisfaction, Patient
  • Hematoma

Interventions

PROCEDURE

Helfer Skin Tap Technique

In a single-group design, 3 technique injections will be administered to the patients, to be randomized. The HST technique will be applied to patients in any one of 1days in a randomized fashion.

PROCEDURE

ShotBlocker Technique

In a single-group design, 3 technique injections will be administered to the patients, 1 technique per week, to be randomized. The ShotBlocker technique will be applied to patients in any one of 1 weeks(3 days) in a randomized manner.

PROCEDURE

Standard Technique

Standard Technique In a single-group design, 3 technique injections will be administered to the patients, 1 technique per days, to be randomized. The standard technique will be applied to patients in any one of 1 weeks in a randomized fashion.

Sponsors & Collaborators

  • Ataturk University

    collaborator OTHER
  • Muş Alparslan University

    lead OTHER

Principal Investigators

  • Bahar Çiftçi · Ataturk University

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-05-01
Primary Completion
2023-08-31
Completion
2023-12-25

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05577832 on ClinicalTrials.gov