Acute coronary syndrome. Ischaemic heart diseases
Conditions
Interventions
Intervention 1: In the intervention group, the patients inhaled three drops of 10% essential oil on an absorbent cloth attached to the patient's collar for 20 minutes. Intervention 2: Control group: I
Sponsors
Gonabad University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Confirmation of acute coronary syndrome by a cardiologist having reading and writing skills mental health satisfaction with the presence in the research having no history of allergy to plants lack of olfactory problems
Exclusion criteria
Exclusion criteria: the patient's death the occurrence of any medical problem requiring immediate medical intervention during the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| State Anxiety. Timepoint: Before the intervention and the first day after the intervention and the second day after the intervention. Method of measurement: Spielberger Anxiety questionnaire.;Adjectival anxiety. Timepoint: Before the intervention and the first day after the intervention and the second day after the intervention. Method of measurement: Spielberger Anxiety questionnaire.;Stress. Timepoint: Before the intervention and the first day after the intervention and the second day after the intervention. Method of measurement: PSS-4 cohen stress questionnaire.;Blood pressure. Timepoint: Before, five, thirty-sixty minutes after the intervention. Method of measurement: Digital SADAT Blood Pressure Measurement Device.;Pulse oximetery. Timepoint: Before, five, thirty-sixty minutes after the intervention. Method of measurement: Monitoring device.;Temperature. Timepoint: Before, five, thirty-sixty minutes after the intervention. Method of measurement: Welch Allyn tympanic thermometer. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAmirreza Nasirzadeh
Gonabad University of Medical Sciences
Outcome results
None listed