Aromatherapy for Reducing Labor Pain

March 16, 2026 updated by: Kuntharee Traisrisilp, Chiang Mai University

Efficacy of Aromatherapy for Reducing Pain During Labor

Pregnant women who eligible with inclusion criteria are random to two groups. Aromatherapy group will receive the aromatherapy during labor along with standard pain control.

Non-aromatherapy group will receive standard pain control during labor

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

94

Phase

  • Not Applicable

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Singleton pregnancy
  • Nulliparous
  • 37 complete weeks of gestation
  • Cephalic presentation
  • No emergency obstetric complication
  • In labor

Exclusion Criteria:

  • Medical or obstetric complication preclude vaginal delivery
  • Essential oil allergy
  • Side effect of aromatherapy

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Aromatherapy
Receive essential oil diffuse by Aroma diffuser during labor. Pain score and dose of analgesics drug are recorded
On the day of admission for labor. Pregnant women select type of essential oil. Aroma diffuser is used during labor. Pain score was record during latent, early active and late active phase.
No Intervention: Non-aromatherapy
This group receive pain control by standard of care without essential oil (aromatherapy)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
early active phase pain using Visual Analog Scale
Time Frame: The day of labor
Visual analog scale used to assess pain during cervical dilate 5-7 cm.
The day of labor

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
latent phase pain using Visual Analog Scale
Time Frame: The day of labor
Visual analog scale used to assess pain during cervical dilate 3-4 cm.
The day of labor
late active phase pain using Visual Analog Scale
Time Frame: The day of labor
Visual analog scale used to assess pain during cervical dilate 8-10 cm.
The day of labor
analgesic drug
Time Frame: The day of labor
doses of analgesic drug request by pregnant women
The day of labor

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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, 2015

Primary Completion (Actual)

December 1, 2016

Study Completion (Actual)

December 1, 2016

Study Registration Dates

First Submitted

March 8, 2017

First Submitted That Met QC Criteria

March 27, 2017

First Posted (Actual)

March 31, 2017

Study Record Updates

Last Update Posted (Actual)

March 18, 2026

Last Update Submitted That Met QC Criteria

March 16, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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.

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