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Effect of Easy Sleep Complex Essential Oil Inhalation on Sleep Disorders

Effect of Easy Sleep Complex Essential Oil Inhalation on Sleep Disorders

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03933553
Enrollment
53
Registered
2019-05-01
Start date
2019-05-04
Completion date
2022-01-17
Last updated
2022-06-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep Disorder

Keywords

aromatherapy essential oil, Easy Sleep complex essential oil, Lavender essential oil, sleep disorders

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.

Interventions

OTHERAromatherapy with essential oil

the aromatherapy by fragrance inhalation

Sponsors

Hung Kaung University
CollaboratorOTHER
Kuang Tien General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
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 5. * 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.

Design outcomes

Primary

MeasureTime frameDescription
The number of sleep gestures during the sleep2 daysAnalyzed with video recording overnight
Electromyogram (EMG)2 daysrecording the electrical activity produced by skeletal muscles
Respiratory effort2 daysThe amplitude change of chest and abdominal movement
Air flow2 daysThe amplitude change of nasal pressure and thermistor
Blood pressure (mmHg)2 daysSystolic and Diastolic blood pressure
Blood oxygen saturation (the fraction of oxygen)2 dayssaturated hemoglobin relative to total hemoglobin in the blood
Heart Rate (beats per minute)2 daysRate of heart beat
Electroencephalogram (EEG)2 daysmeasure 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).
Electrooculograph (EOG)2 daysa record of the difference in electrical charge between the front and back of the eye
Electrocardiogram (ECG)2 daysmeasure heart rate variability (HRV): change of R-R interval

Secondary

MeasureTime frameDescription
Concentration of Interleukin-62 daysblood test with fasting status
Concentration of Interleukin-82 daysblood test with fasting status
Concentration of Tumor necrosis factor-alpha2 daysblood test with fasting status
Concentration of Malonaldehyde2 daysIndicator of oxidative stress
Concentration of Total antioxidant capacity2 daysIndicator of oxidative stress
Concentration of Interleukin-12 daysblood test with fasting status

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026