Effects of Aromatherapy After Aerobic Exercise"
The Effect of Aromatherapy Application on Recovery Speed and Cardiovascular Parameters After Aerobic Exercise in Athletes
1 other identifier
interventional
45
1 country
1
Brief Summary
This study aims to investigate the effect of aromatherapy using lavender oil on recovery speed and cardiovascular parameters in healthy athletes following aerobic exercise. Participants will perform aerobic exercise using the Bruce treadmill protocol and will be randomly assigned to either an aromatherapy group (inhaling lavender essential oil) or a control group (no aromatherapy). Heart rate, blood pressure, oxygen saturation, perceived exertion, and fatigue levels will be measured before and after exercise. The study seeks to determine whether aromatherapy contributes to faster physiological recovery and reduced fatigue following exercise.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2024
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
Study Start
First participant enrolled
January 10, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 16, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
November 10, 2024
CompletedFirst Submitted
Initial submission to the registry
July 18, 2025
CompletedFirst Posted
Study publicly available on registry
July 25, 2025
CompletedJuly 25, 2025
July 1, 2025
9 months
July 18, 2025
July 18, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Heart Rate Recovery
Heart rate was measured using a fingertip pulse oximeter. Participants remained seated and still during the measurements to ensure accuracy. The device provided real-time heart rate readings, recorded manually by the researcher.
Baseline, immediately post-exercise, and at 5 and 15 minutes after recovery
Systolic and Diastolic Blood Pressure
Blood pressure was measured with a calibrated manual sphygmomanometer and a standard stethoscope using the auscultatory method. All measurements were taken from the left arm, with the participant in a seated position, after at least one minute of rest.
Baseline, immediately post-exercise, and at 5 and 15 minutes after recovery
Secondary Outcomes (3)
Oxygen Saturation (SpO₂)
Baseline, immediately post-exercise, and at 5 and 15 minutes after recovery
Rating of Perceived Exertion
Immediately post-exercise and after 15 minutes of recovery
Fatigue Severity Score
Before exercise and after 15 minutes of recovery
Study Arms (3)
Aromatherapy Group
EXPERIMENTALParticipants in this group performed aerobic exercise using the Bruce treadmill protocol. After completing the exercise, they were taken to a separate room where a diffuser had been running for 15 minutes, containing 3 drops of lavender essential oil in 100 ml of water. They inhaled the aromatherapy during a 15-minute recovery period while cardiovascular parameters were monitored.
Placebo Group
PLACEBO COMPARATORParticipants in this group performed aerobic exercise using the Bruce treadmill protocol. After exercise, they were taken to a separate room where a diffuser had been operating for 15 minutes with only 100 ml of plain water and no essential oils. They rested in this environment for 15 minutes, during which their cardiovascular parameters were monitored. This arm aimed to control for the effect of the diffuser itself without the therapeutic component of lavender oil.
Control Group
NO INTERVENTIONParticipants in this group performed aerobic exercise using the Bruce treadmill protocol. After the exercise, they rested in a standard environment without exposure to any diffuser or aromatherapy. Their cardiovascular parameters were monitored during a 15-minute recovery period, serving as the baseline comparison for evaluating the effects of aromatherapy and placebo.
Interventions
Participants inhaled lavender essential oil (3 drops in 100 ml water) via diffuser during a 15-minute post-exercise recovery period following the Bruce treadmill protocol.
Participants were exposed to plain water vapor (100 ml of water without essential oil) via diffuser for 15 minutes during post-exercise recovery.
Eligibility Criteria
You may qualify if:
- Aged between 12 and 14 years
- Actively engaged in organized sports training (minimum 2 times per week)
- Medically cleared to participate in moderate to vigorous physical activity
- No known cardiovascular, respiratory, neurological, or metabolic conditions
- Provided informed assent and obtained written parental/guardian consent
You may not qualify if:
- Known allergy to lavender or any component of aromatherapy oils
- Use of medications that may alter cardiovascular responses (e.g., beta-blockers)
- History of cardiac disease, hypertension, or arrhythmia
- Acute or recent musculoskeletal injury (within the last 3 months)
- Acute upper respiratory tract infection during the assessment week
- Inability to complete treadmill exercise testing or follow instructions
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Bezmialem Vakif University
Istanbul, Turkey (Türkiye)
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SCREENING
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 18, 2025
First Posted
July 25, 2025
Study Start
January 10, 2024
Primary Completion
October 16, 2024
Study Completion
November 10, 2024
Last Updated
July 25, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared due to ethical considerations related to the age group of participants (12-14 years), the sensitivity of health-related information collected, and the limited scope of the study. The study involves minors, and although parental consent and participant assent were obtained, data sharing beyond the primary research team was not included in the consent process. Therefore, data will remain confidential and used solely for the purposes outlined in the approved study protocol.