Actively Recruiting

Phase Not Applicable
Age: 18Years - 49Years
FEMALE
Healthy Volunteers
ID06189794

Effects of Rosa Damascena and Frankincense Essential Oils in Labor

Led by Balikesir University · Updated on 2025-06-18

39

Participants Needed

1

Research Sites

1 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the effects of different essential oils on labor pain, anxiety, and comfort during childbirth. This randomized controlled trial compares the use of rosa damascena oil and frankincense oil to evaluate which one is more effective in improving these experiences for pregnant women. The study focuses on women in labor and aims to provide better understanding of how aromatherapy might influence labor outcomes. Participants will be randomly assigned to one of three groups: rosa damascena oil, frankincense oil, or a placebo solution (0.9% NaCl isotonic solution). The essential oils will be administered by inhalation during labor. The study is single-blinded, meaning the participants do not know which treatment they receive. The trial includes women who are in the latent phase of labor and aged between 18 and 49 years. Women in the study will be monitored for labor pain, anxiety, and childbirth comfort over a three-hour period. These outcomes will be measured to assess the effects of the oils during labor. The research team will collect data during this time to compare the experiences of the different groups. The study is sponsored by Balikesir University and aims to contribute valuable information on non-pharmacological approaches to managing labor discomfort and anxiety.

CONDITIONS

Brief Title

Effects of Rosa Damascena and Frankincense Essential Oils in Labor

Who Can Participate

Age: 18Years - 49Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant women who are at latent phase of labor
Not Eligible

You will not qualify if you...

  • Complicated pregnancy such as preeclampsia, hypertension, or diabetes
  • Planned cesarean section
  • Asthma or any other respiratory disease
  • Allergies to Rosa Damascena or Frankincense oil

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Up to 3 hours during labor

Participants receive inhalation of essential oils during labor to assess effects on pain, anxiety, and comfort.

1 visit (in-person during labor)

Trial Site Locations

Total: 1 location

1

Balikesir University Hospital

Balıkesir, Turkey (Türkiye)

Actively Recruiting

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Research Team

T

Tuba Kızılkaya, Asst.Prof.

E

Esra Cevik, Asst.Prof.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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