Effect of Aromatherapy on Anxiety in Relatives of Emergency Patients.
Principal Investigator, Assistant Professor Şerafettin OKUTAN, Surgical Nursing, Faculty of Health Sciences, Bitlis Eren University
1 other identifier
interventional
120
1 country
1
Brief Summary
This study aims to determine the effect of aromatherapy (lavender oil) application on the anxiety level of relatives of patients admitted to the emergency department. The hypotheses of the study are as follows: H1: Aromatherapy (lavender oil) application has an effect on the anxiety level of relatives of patients presenting to the emergency department. H0: Aromatherapy (lavender oil) application has no effect on the anxiety level of relatives of patients presenting to the emergency department.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Mar 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 5, 2025
CompletedFirst Posted
Study publicly available on registry
January 10, 2025
CompletedStudy Start
First participant enrolled
March 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
October 30, 2025
CompletedFebruary 17, 2026
February 1, 2026
6 months
January 5, 2025
February 12, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
anxiety level
The anxiety levels of patients will be measured using the "State and Trait Anxiety Scale". State and Trait Anxiety Scale; consists of two scales. Each scale has 20 questions. Scoring is between 1-4. Each scale score varies between 20-80 points. A high scale score indicates high anxiety. A low scale score indicates low anxiety.
It will take approximately 30 minutes.
Study Arms (2)
Intervention Group
EXPERIMENTALIntervention Group After the patient is registered in the emergency department, the participant introduction form and state-trait anxiety scales will be applied as a pre-test to the relatives of the patient who agree to participate in the study. The participants will be made to smell lavender oil dropped on gauze by the researchers for an average of 3-5 minutes. The state and trait anxiety scales will be applied as a post-test approximately 15 minutes after the intervention.
Control Group
NO INTERVENTIONControl Group After the patient is registered in the emergency department, the participant introduction form and state-trait anxiety scales will be applied as a pre-test to the relatives of the patient who agree to participate in the study. No intervention will be made to the control group participants. After a certain waiting period (average of 15 minutes), the state and trait anxiety scales will be applied as a post-test.
Interventions
Lavender oil dropped on gauze will be smelled for approximately 3-5 minutes.
Eligibility Criteria
You may qualify if:
- Being 18 years of age or older
- Not having a problem with smell
- Accompanying the patient
- Not having a psychiatric problem
You may not qualify if:
- Refusing to participate in the study or wanting to leave
- Having an upper respiratory tract infection
- Known history of allergy (lavender oil)
- Having a chronic respiratory disease
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Bitlis Eren University
Bitlis, Bitlis, 13100, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Şerafettin OKUTAN, Dr.
Bitlis Eren University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- principal investigator
Study Record Dates
First Submitted
January 5, 2025
First Posted
January 10, 2025
Study Start
March 1, 2025
Primary Completion
September 1, 2025
Study Completion
October 30, 2025
Last Updated
February 17, 2026
Record last verified: 2026-02