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临床试验/NCT05681338
NCT05681338已完成不适用

Effect of the Coughing Technique During Subcutaneous Heparin Injection on Pain Severity and Individual Satisfaction

Uludag University2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年3月17日最近更新:
适应症

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
"Satisfaction assessed by the Visual Individual Satisfaction Scale (VISS)

研究概览

简要总结

Objective: to examine the effect of the medium intensity coughing technique during subcutaneous low molecular weight heparin injection on pain severity and individual satisfaction in general surgery patients. Method: a prospective, quasi-experimental study included 100 patients who had prescribed a subcutaneous low molecular weight heparin injection once in 24 hours. Each patient received two injections by the same researcher using standard injection technique with medium intensity coughing technique and only standard injection technique.

详细描述

Aims and objectives: The aim of this study was to examine the effect on the level of pain severity and satisfaction of patients of the medium intensity coughing technique applied to patients during the administration of subcutaneous low molecular weight heparin (LMWH) injection.

Design: This research was a prospective quasi-experimental study. Methods: It was conducted with 100 patients in the General Surgery Clinic of a university hospital in the Marmara Region of Turkey. Subcutaneous LMWH injections were administered by the same nurse to the outer side of the right and left upper arms by the standard injection technique and the medium intensity coughing technique. Immediately after the subcutaneous LMWH injection was given, a researcher who did not know which injection method had been used asked the patients to evaluate their pain levels by the Visual Analog Scale (VAS) and their satisfaction with the performance of the injection by the Visual Individual Satisfaction Scale (VISS).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Treatment
盲法
Single (Investigator)

盲法说明

The measurements were carried out by the first researcher.

入排标准

年龄范围
22 Years 至 86 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Participating voluntarily in the study
  • Being over the age of 18,
  • Having a doctor's prescription for subcutaneous low molecular weight heparin 0.6 mL treatment and not yet having begun treatment.
  • Having no coagulation disorder, having no disorder that could affect pain perception, -
  • Having no incision, lipodystrophy, or finding of infection at the injection site,
  • Having no communication problem

排除标准

  • Not wanting to participate in the study, or during the course of the research, wishing to withdraw from the study
  • Having any condition which would affect the sensation of pain
  • Not being able to agree on a place or time
  • Being less than 18 years of age

结局指标

主要结局

"Satisfaction assessed by the Visual Individual Satisfaction Scale (VISS)

时间窗: 2 months

During the administration of the injection, an evaluation was made to determine individuals' satisfaction using the Visual Individual Satisfaction Scale, which consisted of a vertical 10 cm scale with "I'm very satisfied" written at one end of it and "I'm not at all satisfied" at the other. The Visual Individual Satisfaction Scale incorporated the characteristics of the well-known Visual Analog Scale (VAS). Satisfaction level measurements were evaluated in millimeters.

Pain assessed by Visual Analog Scale (VAS)

时间窗: 2 months

In evaluating the severity of pain felt by the patients during subcutaneous injections, a 10 cm long vertical VAS was used, on which one end represented no pain, and the other end the worst possible pain. The VAS is a commonly used pain assessment scale in clinical settings. Pain severity measurements were evaluated in millimeters.

次要结局

  • Height(2 months)
  • Weight(2 months)
  • BMI(2 months)

研究者

发起方
Uludag University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dilek Yilmaz, PhD

Bursa Uludag University, Department of Nursing

Uludag University

研究点 (2)

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