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The effect of aroma therapy in heart patients

Not Applicable
Recruiting
Conditions
cardiovascular patients.
Complications and ill-defined descriptions of heart disease
Registration Number
IRCT20160914029817N9
Lead Sponsor
Kerman University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
120
Inclusion Criteria

The patient's willingness to participate in the study and the passage of time is at least 24 hours after the patient's admission
Being over 18 years of age
Earn Points 31 and above Spillberg's Anxiety questionnaire
The absence of sleep disorder before admission (Self-reported by the patient)
Having proper alertness (ability to understand and speak Persian in the language)
No history of any allergies and allergies to herbs and essential oils
Not having olfactory defects and respiratory illnesses, such as asthma
No history of migraine disease
Complete and sign a Consent Form

Exclusion Criteria

A history of known mental illness or taking mental drugs
The history of a new crisis, such as the death of a first-degree relative
Clearance before the fourth day and deterioration of the clinical condition

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Anxiety. Timepoint: Before and after the intervention. Method of measurement: Spilberger State-Trait Anxiety Inventory.;Sleep Quality. Timepoint: Before and after the intervention. Method of measurement: St. Mary's Hospital Sleep Quality Questionnaire.;Vital Signs. Timepoint: Half an hour before the intervention and every 6 hours once during the intervention, except for the patient's bedtime. Method of measurement: Routine registration of vital signs.
Secondary Outcome Measures
NameTimeMethod
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