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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: IRCT
Last refreshed on: 22 February 2018
Main ID:  IRCT2014081718825N1
Date of registration: 2014-09-10
Prospective Registration: No
Primary sponsor: Sabzevar University of Medical Sciences
Public title: The Effects of inhaling lavender oil on anxiety
Scientific title: The Effects of inhaling lavender oil on anxiety level of patients with myocardial infarction
Date of first enrolment: 2014-05-02
Target sample size: 60
Recruitment status: Complete
URL:  http://en.irct.ir/trial/16952
Study type:  interventional
Study design:  Randomization: Randomized, Blinding: Not blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment.  
Phase:  N/A
Countries of recruitment
Iran (Islamic Republic of)
Contacts
Name: Niloofar Mirbastegan   
Address:  School of Nursing and Midwifery, next to the police station to SHahroud road, Sabzevar. Sabzevar Iran (Islamic Republic of)
Telephone: +98 57 1444 6070
Email: Mirbastegan.n@gmail.com
Affiliation:  Sabzevar University of Medical Sciences
Name: Javad Ganjloo   
Address:  School of Nursing and Midwifery, next to the police station to SHahroud road, Sabzevar. Sabzevar Iran (Islamic Republic of)
Telephone: +98 57 1444 6070
Email: jganj@yahoo.com
Affiliation:  Sabzevar University of Medical Sciences
Key inclusion & exclusion criteria
Inclusion criteria: Inclusion criteria: Confirmed diagnosis of Myocardial Infarction(first and second, etc.); Age 30 to 70 years; Not any psychiatric disorder; Not any Alzheimer's disease; Not using anti-anxiety drugs; No drug addiction; Gaining more than 20 of the Spielberg State and trait anxiety questionnaires score; Patient ?agreement for participating in study; Hemodynamic stability. Exclusion criteria: Reluctance to continue participating in the exercises; Sudden change in the patient's hemodynamic status; Having a history of allergies.
Exclusion criteria:

Age minimum: 30 years
Age maximum: 70 years
Gender: Both
Health Condition(s) or Problem(s) studied
Myocardial infarction disease.
Acute myocardial infarction
Acute myocardial infarction
Intervention(s)
Experimental group: The questionnaire of demographic information and Spielberger state and trait anxiety are ?completed before intervention. The intervention group inhaled the essential oil of Lavender for three days for 20-30 minutes, using a non absorbent paper which was stained with three drops of lavender oil, three times a day. The questionnaire of demographic information and Spielberger state and trait anxiety are ?completed after intervention.
Intervention 1: Experimental group: The questionnaire of demographic information and Spielberger state and trait anxiety are ?completed before intervention. The intervention group inhaled the essential oil of Lavender for three days for 20-30 minutes, using a non absorbent paper which was stained with three drops of lavender oil, three times a day. The questionnaire of demographic information and Spielberger state and trait anxiety are ?completed after intervention. Intervention 2: Control group: The questionnaire of demographic information and Spielberger state and trait anxiety are ?completed before intervention. The control group inhaled the distilled water for three days for 20-30 minutes, using a non absorbent paper which was stained with three drops distilled water, three times a day. The questionnaire of demographic information and Spielberger state and trait anxiety are ?completed after intervention.
Control group: The questionnaire of demographic information and Spielberger state and trait anxiety are ?completed before intervention. The control group inhaled the distilled water for three days for 20-30 minutes, using a non absorbent paper which was stained with three drops distilled water, three times a day. The questionnaire of demographic information and Spielberger state and trait anxiety are ?completed after intervention.
Primary Outcome(s)
Anxiety. Timepoint: Before the intervention, 20 to 30 minutes, 3 times a day for 3 days, after intervention. Method of measurement: The questionnaire of Spielberger anxiety ? ?.
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
Sabzevar University of Medical Sciences
Secondary Sponsor(s)
Ethics review
Status: Approved
Approval date:
Contact:
Sabzevar University of Medical Sciences
Results
Results available:
Date Posted:
Date Completed:
URL:
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