"The Effect of Lavender Aromatherapy on Dental Anxiety"
"The Effect of Lavender Aromatherapy on Dental Anxiety-A Randomized Control Trial"
ABSTRACT
Background:
Dental anxiety is addressed as a common issue in adults, often delaying necessary dental treatments and impacting overall oral health. Conventional anxiety management methods may not be preferred due to certain limitations, therefore prompting interest in complementary therapies. The most promising therapy is aromatherapy. Aromatherapy uses essential oils for relaxation to reduce stress. This approach is non-invasive and accessible, making it a promising option for reducing dental anxiety. This study will examine the effect of aromatherapy in adults undergoing dental treatment, highlighting holistic strategies in dental care.
Aim of the study:
This study aimed to determine the effect of aromatherapy on dental anxiety among dental patients.
Methodology:
The study will be a randomized control trial, with 68 participants divided into two groups, Experimental (aromatherapy) and Control, randomizing through Sequentially Numbered, Opaque, and Sealed Envelopes (SNOSE). This trial will be conducted at dental OPD, Dr. Ishrat ul Ebad Khan Institute of Oral Health Sciences. The patients of both gender aged 20-45 years, requiring any dental procedure and providing an informed consent form will be part of the study. Patients with colds, asthma, or other respiratory diseases, acoustic problems, allergic to lavender oils used in the study and mental and physical disabilities will be excluded. It will be a single-blinded study where the examiner is unaware of group allocation. Questionnaires will be used to evaluate patient anxiety levels before the intervention and after dental procedure. Intervention (Aromatherapy) will be administered via nebulizer for 15 minutes. The control group will receive placebo intervention via nebulizer filled with normal saline for 15 minutes. Physiological data will be collected to measure stress response, including systolic and diastolic blood pressure, pulse rate, and oxygen saturation, using a digital sphygmomanometer and pulse oximeter at the start of the intervention (baseline) and at the end of the dental procedure.
研究概览
详细说明
This randomized control trial will be conducted at the Dow University of Health Sciences-Dr. Ishratul Ebad Khan Institute of Oral Health Sciences. It aims to assess the effect of aromatherapy on dental anxiety in dental patients, during dental procedures The study will involve 68 patients aged 20-45, with equal numbers assigned to two groups: Experimental group receiving aromatherapy and control receiving placebo intervention. Participants will be selected using a non-probability convenience sampling technique, with randomization achieved through Sequentially Numbered, Opaque, and Sealed Envelopes (SNOSE). Inclusion criteria include consenting patients of both gender aged 20-45 years and seeking for one of the following dental procedures: root canal treatment, scaling and polishing or tooth extraction for the very first time while patients with respiratory diseases, allergies to lavender oils, or mental and physical disabilities will be excluded. Patient who may refuse to continue the intervention and are non-cooperative will be excluded.
Data collection will include administration of anxiety questionnaires before the intervention and after the procedure. Intervention (Aromatherapy) will be administered via nebulizer for 15 minutes. The control group will receive placebo intervention via nebulizer filled with normal saline for 15 minutes Physiological data such as blood pressure, pulse rate, and oxygen saturation will also be collected to assess the body's stress response.
The sample size was calculated using Open Epi software, with a margin of error of 5% and a significance level of 0.05. Descriptive statistics will summarize the data, while inferential statistics, including paired t-tests and RM will be used for within-group and between-group comparisons, respectively. SPSS version 21 will be used for data analysis, with a significance level set at ≤ 0.05.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Sadaf Arshi, MSc. in Community Dentistry
- 电话号码:02138771111
- 邮箱:sadaf.arshi@duhs.edu.pk
参与标准
资格标准
适合学习的年龄
- 成人
接受健康志愿者
描述
Inclusion Criteria:
- Patients who will give consent to the study.
- Patients aged 20-45 years undergoing dental treatment for the first time.
- Both gender.
- Patient seeking any one of the following dental procedures: root canal treatment, scaling and polishing or tooth extraction.
Exclusion Criteria
- Patients with colds, asthma, and any other respiratory diseases.
- Patients with acoustic problems.
- Patients who are allergic Lavender oils that have been used in this study.
- Patients with mental and physical disabilities.
- Patient who may refuse to continue the intervention will be excluded.
- Non cooperative patients.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Experimental: Aromatherapy will be administered.
Lavender Aromatherapy will administrated to Experimental group
|
Lavender Aromatherapy will administrated to Experimental group
|
|
安慰剂比较:Group 2: (Control): Placebo intervention
|
The control group will receive placebo intervention via nebulizer filled with normal saline for 15 minutes to remain calm and anxiety free.
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Dental anxiety
大体时间:one hour
|
Dental Anxiety status measured by Modified Dental anxiety scale.
The minimum and maximum values recorded by Modified dental anxiety scale will be < 10 and >19 respectively and the higher scores means high dental anxiety which is worse outcome
|
one hour
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Physiological Parameters
大体时间:One hour
|
Both Systolic and Diastolic Blood pressure measured in mm of Hg. . |
One hour
|
|
Physiological Parameter
大体时间:one hour
|
Pulse rate measured as beats per minutes (BPM)
|
one hour
|
|
Physiological Parameter
大体时间:one hour
|
Oxygen saturation measured in %
|
one hour
|
合作者和调查者
出版物和有用的链接
一般刊物
- Karan NB. Influence of lavender oil inhalation on vital signs and anxiety: A randomized clinical trial. Physiol Behav. 2019 Nov 1;211:112676. doi: 10.1016/j.physbeh.2019.112676. Epub 2019 Sep 7.
- Kritsidima M, Newton T, Asimakopoulou K. The effects of lavender scent on dental patient anxiety levels: a cluster randomised-controlled trial. Community Dent Oral Epidemiol. 2010 Feb;38(1):83-7. doi: 10.1111/j.1600-0528.2009.00511.x. Epub 2009 Nov 23.
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
关键字
其他研究编号
- DUHS/IRB/EXTENSION/2026/362
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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