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Effect of inhalation aromatherapy with rose damascene on symptoms of pain, anxiety, and physiological parameters among patients with acute coronary syndrome: a Parallel Randomized Clinical Trial

Effect of inhalation aromatherapy with rose damascene on symptoms of pain, anxiety, and physiological parameters among patients with acute coronary syndrome: a Parallel Randomized Clinical Trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180728040617N9
Enrollment
70
Registered
2023-12-18
Start date
2023-12-22
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

acute coronary syndrome. Acute ischemic heart disease, unspecified

Interventions

Intervention 1: Intervention group: In the aromatherapy group with rose essential oil, 5 drops of 40% rose essential oil will be attached to the patient s shirt and will be placed about 20 cm from th

Sponsors

Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Definitive diagnosis of acute coronary syndrome by a specialist Full consciousness (GCS=15) The patient has been admitted to the emergency ward

Exclusion criteria

Exclusion criteria: Acute psychological disorders Neuroleptic medication Opioid drug consumption before the intervention Allergy to plants and their scent Olfactory disorders

Design outcomes

Primary

MeasureTime frame
Anxiety: Anxiety refers to the score that can be obtained from the Spielberger Anxiety Questionnaire. Timepoint: Before and 10 minutes after the end of the intervention. Method of measurement: Spielberger anxiety questionnaire.;Pain: Pain is the score that can be obtained from the visual analog scale. Timepoint: Before and 10 minutes after the end of the intervention. Method of measurement: visual analog scale.;Physiological indicators: Physiological indicators mean blood pressure, pulse, breathing, temperature and oxygen saturation percentage of arterial blood. Timepoint: Before and 10 minutes after the end of the intervention. Method of measurement: All indicators will be evaluated using Saadat monitoring device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyedmohammad Mirhosseini

Shahroud University of Medical Sciences

mirhoseinim@shmu.ac.ir+98 23 3239 3811

Outcome results

None listed

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