Acute Coronary Syndrom. Acute ischaemic heart disease, unspecified
Conditions
Interventions
Intervention 1: Intervention droup 1:The aroma group , two drops of the blend of Lavender,Roman chamomile and Neroli oils at a ratio of 6:2:0/5 will be shed on pad eye and the patients are asked fr
Treatment - Other
Placebo
Intervention droup 1:The aroma group , two drops of the blend of Lavender,Roman chamomile and Neroli oils at a ratio of 6:2:0/5 will be shed on pad eye and the patients are asked from a distance of
Intervention group 2: placebo group, patients will be received two drops of distilled water on eyepad and the patiens are asked from a distance of 5cm inhale through 10 deep breaths at 7 pm and th
Control group : will be received conventional nursing care.
Sponsors
Vice Chancellor for research of Iran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 80 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Age between 20-80 years; established diagnosis of Unstable Angina and Miocardial Infarction; not having cardiomyopathy; no indication of cardio pulmonary resuscitation; no history of smelling impairments, allergic, rhinitis, eczema, herbal or essence allergic, respiratory disease such as asthma, anxioligic or mental disorders; close relatives death in recent one month; obtaining a score of more than 20 in the Speilberger State Anxiety Inventory; ability to talk and understand Persian; no need for angiography or surgery in next day after intervention; being oriented to person, place and time Exclusion criteria: Lack of consent ti continue study; experienced cardiac dysrhythmia, pain or dyspnea; death during the study; patients who developed allergy to aroma
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Anxiety. Timepoint: 30 min before intervention and 30 min after intervention and following tomorow morning at 7 am. Method of measurement: Spielberger State-Trait Anxiety.;Blood pressure. Timepoint: 30 min before intervention and 30 min after intervention and each 4 hours until following tomorow morning at 7 am. Method of measurement: manitor Novin 51800 saadat co.;Pulse. Timepoint: 30 min before intervention and 30 min after intervention and each 4 hours until following tomorow morning at 7 am. Method of measurement: Pulse count by the researcher in a minute.;Respiration. Timepoint: 30 min before intervention and 30 min after intervention and following tomorow morning at 7 am. Method of measurement: Visit chest going up and down in a minute by researcher. | — |
Secondary
| Measure | Time frame |
|---|---|
| -. Timepoint: -. Method of measurement: -. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactJale Mohammadaliha
Iran University of Medical Sciences-School of Nursing & Midwifery
Outcome results
None listed