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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06193876
Other study ID # 20072023
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 2, 2023
Est. completion date March 15, 2024

Study information

Verified date December 2023
Source Balikesir University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 75
Est. completion date March 15, 2024
Est. primary completion date January 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
Petitgrain and ylang-ylang essential oil
Petitgrain and ylan-ylang essential oil will be dropped to the handchief and students will smell it 3 times in a day.

Locations

Country Name City State
Turkey Osmaniye Korkut Ata University Hospital Osmaniye

Sponsors (1)

Lead Sponsor Collaborator
Tuba Kizilkaya

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary depression level 1 day
Primary stress level 1 day
Primary anxiety level 1 day
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