Effectiveness of Aromatherapy Yoga

Sponsor
Yang Shang-Yu (Other)
Overall Status
Completed
CT.gov ID
NCT05459025
Collaborator
(none)
89
1
2
5
17.7

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Aromatherapy yoga
  • Behavioral: Yoga
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
89 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Effectiveness of Aromatherapy Yoga in Stress Reduction and Sleep Quality Improvement Among Female College Students: A Quasi-Experimental Study
Actual Study Start Date :
Mar 1, 2021
Actual Primary Completion Date :
Jun 1, 2021
Actual Study Completion Date :
Aug 1, 2021

Arms and Interventions

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.

Behavioral: Aromatherapy yoga
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.

Behavioral: Yoga
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.

Outcome Measures

Primary Outcome Measures

  1. Perceived Stress Scale 14 (PSS-14) [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.

  2. Pittsburgh Sleep Quality Index (PSQI) [10-15 minutes]

    The PSQI developed by Buysse et al. [45], which evaluates sleep quality of the participants in the past month.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 21 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Asia Univeraity Taichung WuFeng Taiwan 41354

Sponsors and Collaborators

  • Yang Shang-Yu

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Yang Shang-Yu, Assistant professor, National Cheng Kung University
ClinicalTrials.gov Identifier:
NCT05459025
Other Study ID Numbers:
  • HZAUHU-2021-0001
First Posted:
Jul 14, 2022
Last Update Posted:
Jul 14, 2022
Last Verified:
Jul 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jul 14, 2022