The Effect of ShotBlocker on Pain and Satisfaction During Measles-Rubella-Mumps Vaccination
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 60
- 试验地点
- 2
- 主要终点
- Face, Legs, Activity, Crying, Consolability Pain Scala
研究概览
简要总结
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Health Services Research
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 12 Months 至 12 Months（Child）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •He's 12 months old,
- •MMR vaccine will be administered,
- •growth-development is normal,
- •no analgesic medication was given during the day,
- •at least high school graduate
- •mothers who volunteered to participate in the study
排除标准
- •Neurological disease,
- •a chronic disease,
- •allergy (egg allergy)
- •infants with symptoms of hyperthermia
结局指标
主要结局
Face, Legs, Activity, Crying, Consolability Pain Scala
时间窗: pre-test post-test (approximately three months)
min-max (0-10), lower score means better result, reduce scale scores
次要结局
未报告次要终点
研究者
Veysel Can
Asst. Prof.
Yuzuncu Yıl University