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Effect of Aromathrapy on Anxiety and Severity of Fatigue

A compersion effect of Citrus Aurantium Fragrance and Cranesbill on Anxiety and Severity of Fatigue

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017011824080N10
Enrollment
120
Registered
2017-02-17
Start date
2017-01-20
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

?Acute Myocardial Infarecthion. Myocarditis in diseases classified elsewhere

Interventions

Intervention 1: Aromatherapy start in the second and third days after the attack of acute hemodynamic conditions are Bymarpaydar is and will continue to DAY fourth after admission. For those in the in
Treatment - Drugs
Placebo
Aromatherapy start in the second and third days after the attack of acute hemodynamic conditions are Bymarpaydar is and will continue to DAY fourth after admission. For those in the intervention group
For patients in the placebo group (n = 40) of sunflower oil will be used. each time for 20 minutes is performed.

Sponsors

Lorestan University of Medical Sciences
Lead Sponsor
Lorestan University of Medical Sciences
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: age 18-60 years old; a definite diagnosis of acute heart attack by a physician, and her EC endorsing a heart attack; DNR heart; lung at admission; no history of allergic rhinitis, eczema or respiratory problems such as asthma or chronic obstructive pulmonary disease known; Lack of sense of smell and taste disorders. Lack of medical disorders or uncontrolled contagious. being aware of the time and place and people. Lack of mental illness known. with no history of head injury or seizures. along with a disturbing lack of sleep disorders such as migraine, rheumatoid arthritis, breathing problems at night. having a drug addiction. stable vital signs. having no pain at the time of interview and questionnaire. insensitivity to smell the fragrances; score of more than 20% of Anxiety Inventory (STAI) and the fatigue score between 20 -100 questionnaire MFI-20. Exclusion criteria: the patient's unwillingness to continue the study; cardiogenic shock, cardiac arrest; lung and heart attack this time intervention; a decreased level of consciousness during intervention; the risk of heart rhythm, ventricular fibrillation and cardiogenic shock during the intervention; The use of benzodiazepines, analgesics and anti-anxiety for at least ten hours before the intervention and after the intervention; The use of complementary medicine Sayrdrman for at least a week before the intervention; The incidence of allergic and respiratory dysrhythmias and problems the intervention hemodynamically unstable time intervention patient died before the completion of the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anexity. Timepoint: Half an hour before and 15 minutes after intervention, twice a day. Method of measurement: Questionnaire using the Spielberger.;Fatigue. Timepoint: Half an hour before and half an hour after treatment, twice a day. Method of measurement: Using the questionnaire fatigue Mfi.

Secondary

MeasureTime frame
Headache. Timepoint: An hour after intervention. Method of measurement: Ask the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRaziehShirzadegan

Lorestan University of Medical Sciences

raziehshirzad07@gmail.com00

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026