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临床试验/NCT06769503
NCT06769503已完成不适用

Principal Investigator, Assistant Professor Şerafettin OKUTAN, Surgical Nursing, Faculty of Health Sciences, Bitlis Eren University

Bitlis Eren University1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2025年5月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
120
试验地点
1
主要终点
anxiety level

研究概览

简要总结

This study aims to determine the effect of aromatherapy (lavender oil) application on the anxiety level of relatives of patients admitted to the emergency department.

The hypotheses of the study are as follows:

H1: Aromatherapy (lavender oil) application has an effect on the anxiety level of relatives of patients presenting to the emergency department.

H0: Aromatherapy (lavender oil) application has no effect on the anxiety level of relatives of patients presenting to the emergency department.

详细描述

In the experimental group; After the patient is registered in the emergency department, the participant introduction form and state anxiety scale will be applied as a pre-test to the relatives of the patients who agree to participate in the study. The participants will be made to smell lavender oil dropped on gauze by the researchers for an average of 3-5 minutes. After the intervention, the state anxiety scale will be applied as a post-test approximately 15 minutes later.

In the control group; After the patient is registered in the emergency department, the participant introduction form and state anxiety scale will be applied as a pre-test to the relatives of the patients who agree to participate in the study. No intervention will be made to the participants in the control group. After a certain waiting period (after an average of 15 minutes), the state anxiety scale will be applied as a post-test.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

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

入选标准

  • Being 18 years of age or older
  • Not having a problem with smell
  • Accompanying the patient
  • Not having a psychiatric problem

排除标准

  • Refusing to participate in the study or wanting to leave
  • Having an upper respiratory tract infection
  • Known history of allergy (lavender oil)
  • Having a chronic respiratory disease

研究组 & 干预措施

Intervention Group

Experimental

Intervention Group After the patient is registered in the emergency department, the participant introduction form and state anxiety scale will be applied as a pre-test to the relatives of the patient who agree to participate in the study. The participants will be made to smell lavender oil dropped on gauze by the researchers for an average of 3-5 minutes. The state anxiety scale will be applied as a post-test approximately 15 minutes after the intervention.

干预措施: aromatherapy (Other)

Control Group

No Intervention

Control Group After the patient is registered in the emergency department, the participant introduction form and state anxiety scale will be applied as a pre-test to the relatives of the patient who agree to participate in the study. No intervention will be made to the control group participants. After a certain waiting period (average of 15 minutes), the state anxiety scale will be applied as a post-test.

结局指标

主要结局

anxiety level

时间窗: It will take approximately 30 minutes.

The anxiety levels of patients will be measured using the "State Anxiety Scale". Scale has 20 questions. Scoring is between 1-4. Scale score varies between 20-80 points. A high scale score indicates high anxiety. A low scale score indicates low anxiety.

次要结局

未报告次要终点

研究者

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

Serafettin Okutan

principal investigator

Bitlis Eren University

研究点 (1)

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