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Effect of essential oil of Lavender aromatherapy on anxiety and vital signs in heart ischemia ?patients

?Effect of essential oil of Lavender aromatherapy on anxiety and vital signs in heart ischemia patients ?who hospitalized in CCU

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014030216797N1
Enrollment
80
Registered
2014-05-03
Start date
2014-04-04
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

Ischaemic heart diseases. Acute myocardial infarction

Interventions

The first group (aromatherapy): The questionnaire of demographic information and Spielberger anxiety are ?completed before intervention. Then three drops of pure Lavender oil which were dripped on tis
Treatment - Drugs

Sponsors

Kermanshah University of Medical Sciences?
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: recorded the diagnosis of MI in accordance with physician diagnosis; Suffered from MI for ?the first time; No record of Allergic Rhinitis, Eczema or respiratory problems such as asthma and no olfactory ?dysfunction; No medical or uncontrolled infection disorder; Being aware of time, place and subject; Patient ?agreement for participating in study; No diagnosed mental illness; No drug addiction; the age between 25 to ??65; Stable of vital signs; Having no pain at the time of interview and completing questioner; The ability to ?speak Persian; Gaining more than 20 of the Spielberg State-anxiety questionnaires score. Exclusion criteria: To ?be under CPR on arrival at the ED (emergency department) and CCU; Using sedative drugs without prescription ?during study; Patients suffering cardiac dysrhythmia, ventricular fibrillation, Ventricular tachycardia and ?cardiogenic shock; No cooperation during the study; Patient death during the study; Sensitivity to lavender ?aroma.?

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: Before the intervention, 15 to 20 minutes after intervention in two consecutive days. Method of measurement: The questionnaire of Spielberger anxiety ?.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHossein Ashtarian

Kermanshah University of Medical Sciences

hashtarian@kums.ac.ir+98 83 1827 9796

Outcome results

None listed

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