NCT07258719

Brief Summary

This study aims to investigate the effectiveness of aromatherapy as an intervention to reduce test anxiety and improve academic performance. The Investigators hypothesize that exposure to aromatherapy during assessments will lead to lower levels of test anxiety and result in higher quiz and test scores.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for not_applicable anxiety

Timeline
Completed

Started Sep 2025

Shorter than P25 for not_applicable anxiety

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

September 18, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

November 20, 2025

Completed
12 days until next milestone

First Posted

Study publicly available on registry

December 2, 2025

Completed
16 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 18, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 18, 2025

Completed
Last Updated

February 2, 2026

Status Verified

December 1, 2025

Enrollment Period

3 months

First QC Date

November 20, 2025

Last Update Submit

January 29, 2026

Conditions

Keywords

Aromatherapy

Outcome Measures

Primary Outcomes (6)

  • Change in Westside Test Anxiety Scale (WTAS)

    The WTAS consists of 10 items, each using a Likert response scale where 1= "Never true" and 5= "always true. Total score is divided by 10 to obtain final scores. The total score ranges from one to five with higher scores equating to greater anxiety.

    Baseline and Week 12

  • Change in heart rate (HR) pre aromatherapy

    heart rate will be measured with a fitness tracker before and after quizzes/tests

    week 3 and week 4

  • Change in blood pressure (BP) pre aromatherapy

    both systolic and diastolic blood pressure will be measured with a fitness tracker before and after quizzes/tests

    week 3 and week 4

  • Change in heart rate (HR) with aromatherapy

    heart rate will be measured with a fitness tracker before and after quizzes/tests

    Week 5 through Week 12

  • Change in blood pressure (BP) with aromatherapy

    both systolic and diastolic blood pressure will be measured with a fitness tracker before and after quizzes/tests

    Week 5 through Week 12

  • Change in Stress Performance Evaluation (SPE)

    percent test questions correct (number of test questions correct out of hundred)\]/ percent change in heart rate (heart rate at baseline)/(heart rate after testing) × 100)\]

    Baseline and week 12

Study Arms (2)

aromatherapy intervention 1

EXPERIMENTAL

participants applying their assigned essential oil (ADAPTIV or Thinker) prior to quizzes/tests

Other: Essential Oil 1

aromatherapy intervention 2

EXPERIMENTAL

participants applying their assigned essential oil (ADAPTIV or Thinker) prior to quizzes/tests

Other: Essential Oil 2

Interventions

Participants will complete short tasks before and after quizzes and tests that are part of normal coursework. Prior to each assessment, participants will apply aromatherapy (doTERRA ADAPTIV) using a roller bottle (Weeks 5-12 only), sit quietly for 3 minutes, and record resting Heart Rate and Blood Pressure. T After completing the quiz/test, participants will repeat HR and BP measurements and complete a brief post-assessment questionnaire.

Also known as: ADAPTIV
aromatherapy intervention 1

Participants will complete short tasks before and after quizzes and tests that are part of normal coursework. Prior to each assessment, participants will apply aromatherapy (doTERRA Thinker) using a roller bottle (Weeks 5-12 only), sit quietly for 3 minutes, and record resting Heart Rate and Blood Pressure. T After completing the quiz/test, participants will repeat HR and BP measurements and complete a brief post-assessment questionnaire.

Also known as: Thinker
aromatherapy intervention 2

Eligibility Criteria

Age18 Years - 99 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • current student
  • participating in selected course at the University

You may not qualify if:

  • allergy to essential oils
  • pregnant

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Kentucky

Lexington, Kentucky, 40506, United States

Location

MeSH Terms

Conditions

Anxiety Disorders

Condition Hierarchy (Ancestors)

Mental Disorders

Study Officials

  • Jenalee Hinds, PhD

    University of Kentucky

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

November 20, 2025

First Posted

December 2, 2025

Study Start

September 18, 2025

Primary Completion

December 18, 2025

Study Completion

December 18, 2025

Last Updated

February 2, 2026

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

Locations