- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06193876
The Effect of Aromatherapy Before Clinical Practice on Stress, Anxiety and Depression in Midwifery Students
July 17, 2024 updated by: Tuba Kızılkaya
The Effect of Petitgrain and Ylang-ylang Oil Applied Before Clinical Practice on Stress, Anxiety and Depression in Midwifery Students.
This study was planned as a randomized controlled study to determine the effects of petitgrain and ylang ylang oil applied before clinical practice on stress, anxiety and depression in midwifery students.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
75
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
-
-
-
Osmaniye, Turkey
- Osmaniye Korkut Ata University Hospital
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Being a midwifery student
Exclusion Criteria:
- Having an asthma or any other respiration disease
- Trouble of smelling
- Allergies to petitgrain or ylang-ylang essential oil
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Petitgrain group
In this group petitgrain oil will be used
|
Petitgrain and ylan-ylang essential oil will be dropped to the handchief and students will smell it 3 times in a day.
|
|
Active Comparator: Ylang-ylang group
In this group ylang-ylang oil will be used
|
Petitgrain and ylan-ylang essential oil will be dropped to the handchief and students will smell it 3 times in a day.
|
|
Placebo Comparator: Placebo group
In this group water will be used
|
Petitgrain and ylan-ylang essential oil will be dropped to the handchief and students will smell it 3 times in a day.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
depression level
Time Frame: 1 day
|
1 day
|
|
stress level
Time Frame: 1 day
|
1 day
|
|
anxiety level
Time Frame: 1 day
|
1 day
|
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)
October 2, 2023
Primary Completion (Actual)
January 31, 2024
Study Completion (Actual)
June 15, 2024
Study Registration Dates
First Submitted
December 21, 2023
First Submitted That Met QC Criteria
December 21, 2023
First Posted (Actual)
January 5, 2024
Study Record Updates
Last Update Posted (Actual)
July 18, 2024
Last Update Submitted That Met QC Criteria
July 17, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20072023
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.