- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05459025
Effectiveness of Aromatherapy Yoga
July 12, 2022 updated by: Yang Shang-Yu
Effectiveness of Aromatherapy Yoga in Stress Reduction and Sleep Quality Improvement Among Female College Students: A Quasi-Experimental Study
College students, particularly female students, often suffer from severe stress and poor sleep.
Aromatherapy yoga has become a popular exercise in recent years and may help reduce stress and improve sleep quality, although empirical evidence is limited.
We investigated the effective-ness of aromatherapy yoga intervention in reducing stress and improving sleep quality among female college students.
Eighty-nine participants (44 in the experimental group [aromatherapy yoga] and 45 in the control group [yoga]), with an average age of 19.88 ± 1.13 years, were en-rolled in this quasi-experimental study.
Interventions were performed in the respective groups once a week for 12 weeks, for 90 minutes each time.
The Wilcoxon signed-rank test and Mann-Whitney U test (including effect size) were used to test the differences in stress reduction and sleep quality before and after the intervention.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
89
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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WuFeng
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Taichung, WuFeng, Taiwan, 41354
- Asia Univeraity
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 21 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- We included female college students aged > 18 years, who were able to understand the questionnaire.
Exclusion Criteria:
- We excluded male students, those with a history of respiratory disease, asthma, or allergy to flowers, plants, or essential oils, those who worked at night, and those with a history of mental diseases.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: HEALTH_SERVICES_RESEARCH
- Allocation: NON_RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Aromatherapy yoga
Each intervention session lasted 90 min, between 6 p.m. and 7:30 p.m.
The course was held in a yoga classroom once a week, in an area of 30 m × 35 m.
Furthermore, the total intervention period lasted for 12 weeks.
|
The research assistant diluted the Lavandula angustifolia essential oil with distilled water (1:75) 10 min before the yoga session started.
The solution was then atomized by three aroma diffusers, placed in the front, middle, and back of the classroom.
The distance from each participant was less than 10 m to ensure that the aroma was absorbed com-pletely.
The yoga course for the aromatherapy yoga group was the same as that of the yoga only group.
The yoga group only took a yoga course, without aromatherapy.
|
|
ACTIVE_COMPARATOR: Yoga
Each intervention session lasted 90 min, between 6 p.m. and 7:30 p.m.
The course was held in a yoga classroom once a week, in an area of 30 m × 35 m.
Furthermore, the total intervention period lasted for 12 weeks.
|
The design of the yoga lessons was based on a past study and a professional yoga instruction book.
Yoga lessons were led by certified yoga tutors.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived Stress Scale 14 (PSS-14)
Time Frame: 10-15 minutes
|
PSS-14 is the scale that is most widely used for measuring the degree to which situations in one's life are appraised as being stressful.
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10-15 minutes
|
|
Pittsburgh Sleep Quality Index (PSQI)
Time Frame: 10-15 minutes
|
The PSQI developed by Buysse et al. [45], which evaluates sleep quality of the participants in the past month.
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10-15 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
March 1, 2021
Primary Completion (ACTUAL)
June 1, 2021
Study Completion (ACTUAL)
August 1, 2021
Study Registration Dates
First Submitted
July 12, 2022
First Submitted That Met QC Criteria
July 12, 2022
First Posted (ACTUAL)
July 14, 2022
Study Record Updates
Last Update Posted (ACTUAL)
July 14, 2022
Last Update Submitted That Met QC Criteria
July 12, 2022
Last Verified
July 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- HZAUHU-2021-0001
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.