Aromatherapy's Impact on Test Anxiety in College Students: A Mixed Methods Study
1 other identifier
interventional
20
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable anxiety
Started Sep 2025
Shorter than P25 for not_applicable anxiety
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
Study Start
First participant enrolled
September 18, 2025
CompletedFirst Submitted
Initial submission to the registry
November 20, 2025
CompletedFirst Posted
Study publicly available on registry
December 2, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 18, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 18, 2025
CompletedFebruary 2, 2026
December 1, 2025
3 months
November 20, 2025
January 29, 2026
Conditions
Keywords
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
EXPERIMENTALparticipants applying their assigned essential oil (ADAPTIV or Thinker) prior to quizzes/tests
aromatherapy intervention 2
EXPERIMENTALparticipants applying their assigned essential oil (ADAPTIV or Thinker) prior to quizzes/tests
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.
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.
Eligibility Criteria
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
- Jenalee Hindslead
Study Sites (1)
University of Kentucky
Lexington, Kentucky, 40506, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jenalee Hinds, PhD
University of Kentucky
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