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Comparison between the effect of music therapy and aromatherapy in sleep quality and physiological indices in myocardial infarection patients

Not Applicable
Conditions
myocard infarction.
Acute myocardial infarction
Registration Number
IRCT2015122019919N8
Lead Sponsor
Tabriz University of Medical Sciences (Primary Sponsor)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
129
Inclusion Criteria

inclusion criteria: Would like to participate in the study and signed an informed consent form? male and female patients aged 30 to 75 years who are hospitalized in the intensive care unit with a diagnosis of myocardial infarction? complete consciousness and awareness of time, place or person? Auditory and olfactory disorder, according to the patient and not be a member of the immediate family? History of eczema, hives or respiratory problems such as allergies to flowers and plants and not name? Any serious mental disorder, according to the patient or is not a member of the immediate family? scores from the initial assessment questionnaire Pittsburgh Sleep Quality Index is equal to or less than 5.
Exclusion criteria: Avoid proceeding at any stage of intervention? drug addiction (according to the patient or a family member)? employment health

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improve the quality of life and mean arterial presure. Timepoint: Sleep quality: on the first evening and the morning were the fourth day Inclusion. Method of measurement: Pittsburgh Sleep Quality Index.;Mean arterial presure. Timepoint: One hour before and one hour after 6 am after the intervention and intervention for three consecutive nights. Method of measurement: Using calibrated monitoring devices available in the cardiac care unit.
Secondary Outcome Measures
NameTimeMethod
Improve the physiological (arterial systolic and diastolic blood pressure), body temperature, arterial oxyhemoglobin saturation, heart rate and respiration disease. Timepoint: One hour before and one hour after the experimental intervention and at 6 am after a period of three consecutive nights. Method of measurement: Using standard monitoring devices available in the tympanic thermometer devices.
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