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Effects of Aromatherapy on Childbirth

U

University of Nottingham

Status and phase

Unknown
Phase 2

Conditions

Labor Pain
Natural Childbirth
Parturition

Treatments

Other: None essential oil
Other: Aromatherapy oil

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Aromatherapy is a form of complementary medicine that uses scented materials known as essential oils for the purpose of affecting a person's health or mood. Although aromatherapy has been used in childbirth for centuries, there are no high-quality studies examining whether the treatment works.

Methodology

We would like to see if aromatherapy affects a woman's experience of childbirth by lowering associated anxiety and pain. Consenting participants will be randomly allocated to one of these groups:

  1. Aromatherapy oils (e.g. clary sage, peppermint, lavender, frankincense)
  2. Non-essential oil (baby oil)
  3. Standard maternity care

We will gather primary data, e.g. if she's been in labour before and her awareness of complementary medicine. We will also conduct the Spielberger State-Trait Anxiety Inventory with her, and provide her with the oil and swab if she is in groups 1 or 2 with instructions to keep the swab with the oil on it near to her. She can also put more oil on the swab as she requires.

Postnatally, data will be collected from her notes regarding pain relief used, duration of labour, augmentation of labour, and any other medical interventions of note. We will also complete the anxiety scale with her once more. Before her discharge we ask the mother for any comments regarding her experience of the labour. The results from all three cohorts will then be compared. There will also be opportunity for the midwife to make any comments regarding his/her perception of the participant's labour. Finally we will hold a focus group with midwives regarding the practicalities for implementation of aromatherapy in maternity care

Enrollment

90 estimated patients

Sex

Female

Ages

16 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • women in labour and expecting a normal delivery,
  • aged > 16 who are able to make informed consent;
  • singleton pregnancy;
  • spontaneous or induced labour onset;
  • prior to elective or emergency caesarean section.

Exclusion criteria

  • preterm labour;
  • pool births;
  • scheduled caesarean section.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

90 participants in 3 patient groups, including a placebo group

Aromatherapy group 1
Experimental group
Description:
Participants will be given essential oil consisting of (Peppermint, Lavender, Clary Sage and Frankincense) together with a swab to put the oil on.
Treatment:
Other: Aromatherapy oil
Control group 2
Placebo Comparator group
Description:
Participants receive a bottle of non essential oil and a swab.
Treatment:
Other: None essential oil
Control group 3
No Intervention group
Description:
Standard maternity care to measure baseline.

Trial contacts and locations

1

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Central trial contact

Dawn-Marie Walker, BSc MSc PhD

Data sourced from clinicaltrials.gov

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