ShotBlocker, Cold Needling, and Both Methods in Combination Pain and Satisfaction
NCT07258953 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 132
Last updated 2026-05-18
Summary
Intramuscular (IM) injections are one of the most frequently used pharmacological treatment methods in nursing practice. Reducing the pain experienced by patients during this procedure and ensuring patient satisfaction are important indicators of treatment quality. Reducing injection-related pain should be a priority in nursing care for both patient safety and the effectiveness of the treatment process.
This study is a trpile-blind, randomized, controlled trial. It was designed to evaluate the effects of ShotBlocker, cold needle, and a combination of both methods during intramuscular injection on patient pain levels and satisfaction. The research will be conducted in the injection unit affiliated with the Adult Emergency Department of Konya City Hospital, Ministry of Health of the Republic of Turkey. The study population will consist of patients who presented for cyanocobalamin injections, and the sample will consist of 132 individuals who voluntarily agreed to participate in the study and met the inclusion criteria. Before conducting the study, ethical approval will be obtained from the Necmettin Erbakan University Health Sciences Ethics Committee and from the Konya City Hospital of the Ministry of Health of the Republic of Turkey. Collected data will be analyzed using the SPSS statistical package program (version 22.0; SPSS Inc., USA). The Kolmogorov-Smirnov test will be used to assess whether the data exhibit a normal distribution; statistical significance will be accepted as p\<0.05.
Conditions
Interventions
- OTHER
-
ShotBlocker+cold needle
During intramuscular injection, ShotBlocker and the cold needle will be used simultaneously.
- OTHER
-
Cold needle
A cold needle will be used during intramuscular injection.
- OTHER
-
ShotBlokcer
ShotBlocker will be used during intramuscular injection.
- OTHER
-
Control
Intramuscular injection will be conducted according to standard technique.
Sponsors & Collaborators
-
Necmettin Erbakan University
lead OTHER
Principal Investigators
-
Yadigar Yadigar · Necmettin Erbakan University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- SUPPORTIVE_CARE
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-01-01
- Primary Completion
- 2026-04-01
- Completion
- 2026-05-04
Countries
- Turkey (Türkiye)
Study Locations
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