Skip to content

The Effect of aromatherapy with Lavender on sleep quality among patients undergoing Coronary Artery Bypass Graft in Semnan Kowsar Hospital

Aromatherapy with Lavender on sleep quality patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017060811399N6
Enrollment
60
Registered
2017-06-12
Start date
2017-07-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Sleep disorder. Disorders of initiating and maintaining sleep [insomnias]

Interventions

Intervention 1: In the intervention group, Lavender will be dropped on a cotton ball at a rate of 2 drops and Will be kept in front of the patient's nose and patients will be asked to breathe 10 time
Treatment - Other
Placebo
In the intervention group, Lavender will be dropped on a cotton ball at a rate of 2 drops and Will be kept in front of the patient's nose and patients will be asked to breathe 10 time deeply and in th
In the control group, distilled water will be dropped on a cotton ball at a rate of 2 drops and will be kept in front of the patient's nose and he will be asked to take 10 deep breaths and in the foll

Sponsors

Vice chancellor for research, Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: The patients' willingness to participate in the study; Undergoing non-emergency open heart surgery for the first time; Aged between 30 and 75 years old; Stable hemodynamic condition such as systolic blood pressure higher than 90 mmHg; lack of life threatening dysrhythmia and a heart rate between 60 and 100 bpm; Not drug and alcohol addicted; lack of confirmed mental illness; No history of known allergies to lavender or seasonal allergy; lack of olfactory disorders; Lack of respiratory disorders such as asthma; Being conscious and oriented to time; Place and person and having the ability to complete hearing and speech. Exclusion criteria: Taking the sedative in addition to routine treatments; life threatening dysrhythmias or any emergency conditions requiring immediate intervention; loss of the patient’s consciousness; The patient’s willingness to quit from the study; allergy to lavender or any allergic reaction during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Patients sleep quality after coronary artery bypass graft. Timepoint: Daily, during 4 days. Method of measurement: Hospital sleep quality questionnaire.

Secondary

MeasureTime frame
Sleep quality after water inhalation. Timepoint: Daily, during 4 days. Method of measurement: Hospital sleep quality questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHossein Davari

Semnan University of Medical Sciences

hosseindavari30@yahoo.com+98 23 3343 7825

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026