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Clinical Trials/NCT03933553
NCT03933553CompletedNot Applicable

Effect of Easy Sleep Complex Essential Oil Inhalation on Sleep Disorders

Kuang Tien General Hospital1 site in 1 country53 target enrollmentStarted: May 4, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
53
Locations
1
Primary Endpoint
Electroencephalogram (EEG)

Study Overview

Brief Summary

Sleep disorders affect human health tremendously. It has been reported that aromatherapy by fragrance inhalation can be used as an adjuvant therapy to modulate parasympathetic nervous activity for relieving stress and mood, and promoting sleep quality. Many researches confirmed that lavender essential oil can be used as an adjuvant therapy for sleep disorders. It can effectively relieve stress and modulate physical and mental status. However, many studies about aromatherapy lack sleep detection instruments to objectively confirm their effects on sleep physiology. Therefore, this study adopts Easy sleep complex essential oil as the experimental group. The lavender essential oil containing orange, petitgrain, rose, lavender, rosewood, ho wood, amyris essential oil and lavender oil is chosen as control group. The subjects will be randomly assigned to one of the two groups. The efficacy results will be evaluated and compared between the two groups. The investigators expect that aromatherapy by fragrance inhalation with Easy sleep complex essential oil will improve sleep quality more effectively than lavender essential oil.

Detailed Description

A Randomized, Single-blind, Active-Controlled Trial to Evaluate the aromatherapy by fragrance inhalation using Easy sleep complex essential oil in patients with sleep disorders.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
20 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •The subjects who signs the informed consent form approved by the Institutional Review Board.
  • •Adult between the ages of 20-65 with the ability to communicate and describe symptoms.
  • •The subjects has sleep disorders that last for at least three months and more than three nights per week.
  • •Pittsburgh Sleep Quality Index(PSQI) score greater than
  • •The subjects are willing to cooperate with the study requirements, examinations and tests, including aromatherapy, polysomnography for two consecutive nights, questionnaire and blood tests.

Exclusion Criteria

  • •The patients with abnormal olfactory system such as brain injury, acute or chronic sinusitis, and the history of nasal surgery.
  • •Patients who are currently taking sedatives or stimulant medicine or food such as coffee or refresh drink.
  • •Patients with a known history of allergy to aromatherapy or asthma.
  • •Patients has severe cardiovascular or pulmonary disease (e.g., cardiac failure or lung failure), or has cancer or other critical illness (e.g., renal dialysis).
  • •Pregnant or breastfeeding women.

Arms & Interventions

Lavender essential oil

Active Comparator

Aromatherapy for 2 hours starting 10 minutes before sleep with 5 drops of the essential oil diluted in 50ml water

Intervention: Aromatherapy with essential oil (Other)

Easy sleep complex essential oil

Experimental

Aromatherapy for 2 hours starting 10 minutes before sleep with 5 drops of the essential oil diluted in 50ml water

Intervention: Aromatherapy with essential oil (Other)

Outcomes

Primary Outcomes

Electroencephalogram (EEG)

Time Frame: 2 days

measure the alpha wave(8-14Hz), Vertex sharp wave(4-7Hz), K complex (negative- positive sharp component area), Spindle(7-14Hz for at least 0.5 sec), theta wave(4-7Hz), and delta wave(0.5-3Hz, amplitude\>75uV).

Respiratory effort

Time Frame: 2 days

The amplitude change of chest and abdominal movement

Air flow

Time Frame: 2 days

The amplitude change of nasal pressure and thermistor

Electrooculograph (EOG)

Time Frame: 2 days

a record of the difference in electrical charge between the front and back of the eye

Electrocardiogram (ECG)

Time Frame: 2 days

measure heart rate variability (HRV): change of R-R interval

Electromyogram (EMG)

Time Frame: 2 days

recording the electrical activity produced by skeletal muscles

Blood pressure (mmHg)

Time Frame: 2 days

Systolic and Diastolic blood pressure

Blood oxygen saturation (the fraction of oxygen)

Time Frame: 2 days

saturated hemoglobin relative to total hemoglobin in the blood

Heart Rate (beats per minute)

Time Frame: 2 days

Rate of heart beat

The number of sleep gestures during the sleep

Time Frame: 2 days

Analyzed with video recording overnight

Secondary Outcomes

  • Concentration of Interleukin-6(2 days)
  • Concentration of Interleukin-8(2 days)
  • Concentration of Tumor necrosis factor-alpha(2 days)
  • Concentration of Interleukin-1(2 days)
  • Concentration of Malonaldehyde(2 days)
  • Concentration of Total antioxidant capacity(2 days)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Chun-pai Yang, MD

Head of Sleep Center

Kuang Tien General Hospital

Study Sites (1)

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