Heart Disease. Ischemic Heart Disease
Conditions
Interventions
Intervention 1: Intervention group: Aroma "Citrus aurantium" was prepared by Research Institute of Forests and Rangelands, Tehran, and diluted with sun flower oil to 10 percent of dilution. For three
Treatment - Other
Placebo
Intervention group: Aroma "Citrus aurantium" was prepared by Research Institute of Forests and Rangelands, Tehran, and diluted with sun flower oil to 10 percent of dilution. For three consecutive nigh
Control group: Pure sun flower oil, for three consecutive nights using the inhalation, every night is poured three drops on a tissue and inhale three deep breath by patient. SMHSQ before and after wil
Sponsors
Vice chancellor for research, Qazvin University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Hospitalized patients with the Clinical diagnosis of heart disease in intensive coronary care unit. Having a strong natural tendency for cooperation in doing some medical research and signing the Informed Consent form for research. Stable vital signs ((blood pressure, pulse, respiration, temperature) Patients aged over 18 and under 65. Patients with no medical histories of mental illness having led to a long period hospitalization and the consumption of psychiatric drugs. No use of herbal medicines in the past two weeks. Having no allergic histories to medicines and all herbs (Herbal Medicines or Herbal remedies) No allergy symptoms were caused about all the medicines they had taken in the allergy tests. Positive indicators of Epworth Questionnaire (score>5) To have taken “Berlin questionnaire for sleep apnea” to be positive. Exclusion Criteria: Vital sign instability which leads to a change in drug instructions. Dosage change and the sedative drugs deletion, if desired. The transference of patients from the Cardiac Care Unit to the other wards. To be discharged from the hospital –doctor’s orders or against medical advice. To display no tendencies to cooperate on the research any longer. Allergy symptoms are to be caused.
Exclusion criteria
Exclusion criteria:
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Sensitivity to Citrus Aurantium L. essence. Timepoint: 2 hours preintervention- every 3 hours during intervention and 2 hours post intervention. Method of measurement: Clinical signs and symptoms. | — |
Primary
| Measure | Time frame |
|---|---|
| Sleep Quality. Timepoint: 2 hours preintervention - 3 days post intervention. Method of measurement: St Marry's Hospital Sleep Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFariba Mohamadi Hariry
Qazvin University of Medical Science
Outcome results
None listed