ClinicalTrials.gg
CompletedNCT07922304Updated Nov 6, 2026

Aroma Inhalation and Exam Stress: Role of Emotional Intelligence and Stress Biomarkers

An interventional study of Juniper Aromatherapy and Thyme Aromatherapy in Exam-induced Psychological Stress, Emotional Intelligence and Physiological Stress Responses in Healthy University Students, sponsored by Gulbahar Boyuk Ozcan. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 25 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-06.

Sponsored by Gulbahar Boyuk Ozcan · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year after the study started (first participant enrolled Jun 2024, registered Jul 2025).
Updated Nov 6, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
94
Allocation
Non-randomized
Ages
18 Years to 25 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 39 studies in Stress, Psychological with a site in Turkey — 9 open to participants now, 12 under way, none of them phase 3. Stress, Psychological · Turkey.

Enrollment
15th of 33
94 · median 80
Started
2024
with 6 others
No phase
33 of 39
7 open now
Registered
20th of 39
by date
Lead sponsor
2 of 39
Gulbahar Boyuk Ozcan

Among the 39 studies in Stress, Psychological with a site in Turkey, this one is the 15th largest by enrollment of the 33 interventional ones that give a count, is one of 7 that started in 2024, is one of 33 with no phase, and was the 20th registered.

Stress, Psychological

848 studies on the registry are indexed under Stress, Psychological; 139 are open to participants now.

Browse Stress, Psychological studies →

Open to participants now

9 of the 39 studies in Stress, Psychological with a site in Turkey are open now. Recruiting first, the newest first:

4 more — sign in →

All 9 open studies →

A study can be open while its sites in Turkey have not opened yet or have stopped. Only those recruiting at a site in Turkey →

Who these studies take

Of the 75 Stress, Psychological studies recruiting now, 34 (45%) set no upper age limit and 37 (49%) stop at 75 or younger; 14 take children under 18; 49 take healthy volunteers.

This study: 18 Years to 25 Years · all sexes · healthy volunteers too.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 39 studies in Stress, Psychological with a site in Turkey, or all of them as a file.
02

Study summary

This study is an interventional investigation aiming to evaluate the physiological effects of thyme (Thymus vulgaris) and juniper (Juniperus communis) essential oil aroma inhalation on examination stress in medical students. The research assesses participants' emotional intelligence and exam anxiety levels, and analyzes changes in salivary apelin, BDNF, and GRP78 levels using the ELISA method before and after the aromatherapy intervention.

Read the detailed description

Study Purpose: This study aims to investigate the effects of aroma inhalations (thyme and juniper) on exam stress, adipokines (apelin), neurotrophic factors (BDNF), and endoplasmic reticulum stress responses (GRP78) based on emotional intelligence and exam anxiety levels in medical students. Methods: The study is a three-arm, randomized, controlled interventional investigation conducted on healthy volunteer medical students. Saliva samples are collected before inhalation and immediately after the 15-minute intervention. The ELISA technique is utilized to determine salivary apelin, BDNF, and GRP78 levels.

03

Conditions studied

  • Exam-induced Psychological Stress
  • Emotional Intelligence
  • Physiological Stress Responses in Healthy University Students

Browse trials for

Keywords

  • Aroma inhalation
  • Thyme essential oil
  • Juniper essential oil
  • Exam stress
  • Emotional intelligence
  • Exam anxiety
  • Apelin
  • BDNF
  • GRP78
  • Stress biomarkers
  • Salivary biomarkers
  • Cognitive support
  • University students
  • ELISA
  • Stress management
04

Who can participate

Ages eligible
18 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Being willing to participate in the research, being a medical student, not having a cardiovascular disease, not having any allergies to odors, not being pregnant, not having any respiratory system diseases (such as asthma, , etc.), not having any condition that prevents smelling, not using any medication that affects heart rate and blood pressure, and not having any psychiatric illness.

Exclusion criteria

Exclusion Criteria:

The communication barrier, incomplete filling of forms, menstruation in girls, allergy to the scents of thyme and juniper oil, and the occurrence of any side effects during the application.

Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

COPD

Chronic obstructive pulmonary disease: long-term lung disease that makes it hard to breathe out, including emphysema and chronic bronchitis.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
94 participants (actual)

Study arms

  • Experimental
    Juniper Aromatherapy Group

    Participants inhale juniper essential oil for 40 minutes during the exam. Physiological and hormonal measurements are taken before and after inhalation.

    Other: Juniper Aromatherapy

  • Experimental
    Thyme Aromatherapy Group

    Participants inhale thyme essential oil for 40 minutes during the exam. Physiological and hormonal measurements are taken before and after inhalation.

    Other: Thyme Aromatherapy

Interventions

  • OtherJuniper Aromatherapy

    Participants inhale juniper essential oil (2 drops) via a diffuser or inhaler for approximately 40 minutes during the exam session. This inhalation is intended to assess effects on anxiety-related physiological and hormonal parameters.

  • OtherThyme Aromatherapy

    Participants inhale thyme essential oil (2 drops) via a diffuser or inhaler for approximately 40 minutes during the exam session. This inhalation is intended to assess effects on anxiety-related physiological and hormonal parameters.

06

What researchers measure

Primary outcomes

  1. Change in Salivary Apelin Levels

    Salivary apelin levels will be measured to evaluate the metabolic and neuroendocrine response to aroma inhalation.

    Time frame: Immediately before inhalation and immediately after the 15-minute inhalation intervention

  2. Change in Salivary BDNF Levels

    Salivary BDNF levels will be measured as a neurotrophic and physiological stress indicator.

    Time frame: Immediately before inhalation and immediately after the 15-minute inhalation intervention

  3. Change in Salivary GRP78 Levels

    Salivary GRP78 levels will be measured to monitor cellular endoplasmic reticulum stress responses.

    Time frame: Immediately before inhalation and immediately after the 15-minute inhalation intervention

07

Study locations

1 site
  • Ankara Medipol University
    Ankara, Altindag 06050, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No — The individual participant data (IPD) will not be shared due to ethical considerations and institutional restrictions.

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Jun 2024 to primary completion in Jun 2024, 0 months.

Of 459 non-industry interventional studies with no phase under Stress, Psychological, half reached primary completion within 13 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 26. This study's 0 months is below that.

Counting every sponsor, half of 472 studies reached it within 13 months; a quarter within 5 and three quarters within 26.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 9, 2025
First posted
Nov 6, 2026
StartActual
Jun 20, 2024
Primary completionActual
Jun 30, 2024
CompletionActual
Dec 15, 2024
Last update
Nov 6, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 6, 2026
Show all 1 update
  1. Nov 6, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07922304
Lead sponsor
Gulbahar Boyuk Ozcan
Responsible party
Gulbahar Boyuk Ozcan (Ankara Medipol University Faculty of Medicine, Ankara Medipol University) — Sponsor-investigator
First posted
Nov 6, 2026
Start date
Jun 20, 2024
Primary completion
Jun 30, 2024
Completion
Dec 15, 2024
Last update
Nov 6, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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