Aromatherapy for Reducing Labor Pain
Efficacy of Aromatherapy for Reducing Pain During Labor
1 other identifier
interventional
94
0 countries
N/A
Brief Summary
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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable pain
Started Mar 2015
Typical duration for not_applicable pain
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2016
CompletedFirst Submitted
Initial submission to the registry
March 8, 2017
CompletedFirst Posted
Study publicly available on registry
March 31, 2017
CompletedMarch 18, 2026
March 1, 2026
1.8 years
March 8, 2017
March 16, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
early active phase pain using Visual Analog Scale
Visual analog scale used to assess pain during cervical dilate 5-7 cm.
The day of labor
Secondary Outcomes (3)
latent phase pain using Visual Analog Scale
The day of labor
late active phase pain using Visual Analog Scale
The day of labor
analgesic drug
The day of labor
Study Arms (2)
Aromatherapy
EXPERIMENTALReceive essential oil diffuse by Aroma diffuser during labor. Pain score and dose of analgesics drug are recorded
Non-aromatherapy
NO INTERVENTIONThis group receive pain control by standard of care without essential oil (aromatherapy)
Interventions
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.
Eligibility Criteria
You may qualify if:
- Singleton pregnancy
- Nulliparous
- complete weeks of gestation
- Cephalic presentation
- No emergency obstetric complication
- In labor
You may not qualify if:
- Medical or obstetric complication preclude vaginal delivery
- Essential oil allergy
- Side effect of aromatherapy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principle investigator
Study Record Dates
First Submitted
March 8, 2017
First Posted
March 31, 2017
Study Start
March 1, 2015
Primary Completion
December 1, 2016
Study Completion
December 1, 2016
Last Updated
March 18, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share