Principal Investigator, Assistant Professor Şerafettin OKUTAN, Surgical Nursing, Faculty of Health Sciences, Bitlis Eren University
概览
- 阶段
- 不适用
- 干预措施
- aromatherapy
- 疾病 / 适应症
- Emergency Service, Hospital
- 发起方
- Bitlis Eren University
- 入组人数
- 120
- 试验地点
- 1
- 主要终点
- anxiety level
- 状态
- 已完成
- 最后更新
- 2个月前
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-trait anxiety scales 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 and trait anxiety scales 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-trait anxiety scales 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 and trait anxiety scales will be applied as a post-test.
研究者
Serafettin Okutan
principal investigator
Bitlis Eren University
入排标准
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
Intervention Group After the patient is registered in the emergency department, the participant introduction form and state-trait anxiety scales 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 and trait anxiety scales will be applied as a post-test approximately 15 minutes after the intervention.
干预措施: aromatherapy
Control Group
Control Group After the patient is registered in the emergency department, the participant introduction form and state-trait anxiety scales 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 and trait anxiety scales 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 and Trait Anxiety Scale". State and Trait Anxiety Scale; consists of two scales. Each scale has 20 questions. Scoring is between 1-4. Each scale score varies between 20-80 points. A high scale score indicates high anxiety. A low scale score indicates low anxiety.