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Study on the Efficacy of Vetiver Essential Oil Aroma on Depression/Anxiety People

C

Chung Shan Medical University

Status

Enrolling

Conditions

Anxiety Depression Disorder

Treatments

Device: Limon essential oil aromatherapy
Device: Vetiver essential oil aromatherapy

Study type

Interventional

Funder types

Other

Identifiers

NCT05024136
CS1-20030

Details and patient eligibility

About

In this study, subjects with depression/anxiety inhaled the essential oil, which contained sedative, soothing, and relaxing active ingredients to stimulate the olfactory nerve. The essential oil further transmitted to the limbic system that controls emotions in the brain, and then affected the human's mood. The natural aroma can not only awaken the limbic system's memory of aroma but also reflect the subconscious area of the brain, with physiological changes (such as controlling blood pressure, breathing, heartbeat, stress changes, memory, and hormonal coordination.) This study monitors the subject's autonomic nerve parameters before and after aromatherapy to obtain the olfactory cerebral nervous system to convey the message. When the study finishes, we expected to help the subject to relax and soothe the mind.

Full description

Subjects receive three times 30 mins aromatherapy of Limon or Vetiver essential oil per time for the month. Anthropometric measurements such as blood pressure (systolic blood pressure [SBP] and diastolic blood pressure [DBP]), autonomic nerve parameters including a. SDNN (standard deviation of all normal to normal intervals index); b. HRV(heart rate variability); c. LF(0.04-0.15 Hz)and HF(0.15-0.4 Hz)were measured every week. PSQI(Pittsburgh sleep quality index)and HADS (Hospital Anxiety and Depression Scale) were measured initial and ten ends.

Enrollment

60 estimated patients

Sex

All

Ages

20 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Depressed/anxious people (diagnosed as a single episode of major depression, recurrence of major depression, mild depression, panic disorder, and anxiety.) Those diagnosed with symptoms of depression, and anxiety related to stress adjustment disorder, and willing to cooperate with the study.
  2. Age 20-65 years old

Exclusion criteria

  1. an alcoholic
  2. Uncontrolled diabetes
  3. Those who have had a stroke in the last year
  4. Pregnant and lactating women
  5. People with liver or heart disease
  6. Arrhythmia or those with a heart rhythm regulator
  7. Those whose heart has already been fitted with a cardiac catheter stent
  8. Those who have used central nervous system stimulants (regardless of the length of time)
  9. Those who are allergic to essential oils
  10. Those who have used aromatherapy within a month
  11. Subjects request to withdraw from the trial
  12. The host feels unsuitable to continue the study

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

Placebo
Active Comparator group
Description:
Subjects take 30 mins aromatherapy of Limon essential oil per time, a total of 3 times for the month.
Treatment:
Device: Limon essential oil aromatherapy
Experimental
Experimental group
Description:
Subjects take 30 mins aromatherapy of vetiver essential oil per time, a total of 3 times for the month.
Treatment:
Device: Vetiver essential oil aromatherapy

Trial contacts and locations

1

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Central trial contact

You-Cheng Mr Shen, Ph.D.; Chang-Yao Mr TSAO, MD/PhD.

Data sourced from clinicaltrials.gov

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