Trials / Completed
CompletedNCT06762938
The Effect of ShotBlocker on Pain and Satisfaction During Measles-Rubella-Mumps Vaccination
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- Yuzuncu Yil University · Academic / Other
- Sex
- All
- Age
- 12 Months – 12 Months
- Healthy volunteers
- Accepted
Summary
Objective The aim of this study was to evaluate the effects of ShotBlocker administration during measles-mumps-rubella (MMR) vaccination on infants' pain level and mothers' satisfaction. Method. The study was conducted in a Family Health Center affiliated to the Public Health Directorate of a province in eastern Turkey between August and October 2024 using a randomized controlled experimental design. The study sample consisted of 60 infants who received MMR vaccination (ShotBlocker group: n = 30, control group: n = 30). Infants in the ShotBlocker group received ShotBlocker before vaccine injection, while infants in the control group received only routine vaccine injection. Infant information form, FLACC pain scale and Newcastle Satisfaction with Nursing Care Scale were used for data collection. Ethical principles were followed throughout the study.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BEHAVIORAL | ShotBlocker | Apply ShotBlocker |
Timeline
- Start date
- 2024-08-01
- Primary completion
- 2024-11-20
- Completion
- 2024-11-30
- First posted
- 2025-01-08
- Last updated
- 2025-01-08
Locations
1 site across 1 country: Turkey (Türkiye)
Source: ClinicalTrials.gov record NCT06762938. Inclusion in this directory is not an endorsement.