acute cronary syndrome. Acute ischaemic heart disease, unspecified
Conditions
Interventions
Intervention 1: The intervention group patients' anxiety is measured by a questionnaire.
6 drops of citrus aurantium 30 percent on a piece of gauze.
For twenty minutes we hung patient's collar.
Do thi
Placebo
The intervention group patients' anxiety is measured by a questionnaire.
6 drops of citrus aurantium 30 percent on a piece of gauze.
For twenty minutes we hung patient's collar.
Do this twice a day
Patients in the control group measured anxiety.
The aromatherapy is done with liquid paraffin as placebo
Six drops of placebo on small gas spills
For twenty minutes we hung patient's collar.
This
Sponsors
Shahed University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Inclusion criteria? a diagnosis of acute coronary syndrome?satisfaction and interest in participating in the study?lack of active mental illness and mental retardation?deafness? blindness? problems of smell? lack of sensitivity to aurantium? no drug Exclusion criteria? patient's unwillingness to continue the study? discharge and transfer patients to other centers
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| ANXIETY. Timepoint: Smooth over the intervention and 12 hours after intervention. Method of measurement: Anxiety Inventory Spielberger. | — |
Secondary
| Measure | Time frame |
|---|---|
| Depression. Timepoint: Before and after intervention. Method of measurement: Beck depression questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFarhadMoslemi
Nursing College of Shahed
Outcome results
None listed