Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07126301

Aromatherapy Essential Oils to Manage Anxiety and Nausea in Cancer Patients Receiving Infusion in the Ambulatory Setting

Led by City of Hope Medical Center · Updated on 2025-08-17

60

Participants Needed

2

Research Sites

77 weeks

Total Duration

On this page

Sponsors

C

City of Hope Medical Center

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This clinical trial tests how well aromatherapy essential oils work to manage anxiety and nausea in cancer patients receiving infusions in the ambulatory setting. Current drugs that are given for nausea may cause constipation and fatigue. Therefore, there is interest in exploring complementary therapies, like aromatherapy, that do not carry the same side effects. Using aromatherapy essential oils such as ginger, peppermint, and lavender, may help reduce nausea and anxiety. Some studies have shown significant reductions in nausea and anxiety among cancer patients using these oils, while other studies have had mixed results. Ginger and peppermint oils, in particular, have been associated with helping reduce nausea during chemotherapy, while lavender has shown potential benefits for anxiety. Jojoba oil will be used as a placebo for this research study. Jojoba oil is extracted from the seeds of a jojoba plant, which is a green shrub that is found in the southwestern United States). Jojoba oil is an oil which has no color or smell. Aromatherapy essential oils used through a personal inhalation device during chemotherapy may better manage anxiety and nausea in cancer patients receiving infusions in the ambulatory setting.

CONDITIONS

Official Title

Aromatherapy Essential Oils to Manage Anxiety and Nausea in Cancer Patients Receiving Infusion in the Ambulatory Setting

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients must be able to understand and sign informed consent and follow study instructions
  • Ability to read and understand English for patient-reported outcomes
  • Age 18 years or older
  • Eastern Cooperative Oncology Group (ECOG) performance status of 2 or less
  • Willing to comply with all aromatherapy essential oil treatments
  • Receiving moderate- to high-risk emetogenic chemotherapy as defined by NCCN for at least one cycle
  • Have at least two remaining chemotherapy infusion appointments on a moderate- to high-risk regimen
  • Experienced nausea greater than 3 out of 10 with last chemotherapy infusion
  • Open to all genders, races, and ethnicities
Not Eligible

You will not qualify if you...

  • Self-reported sensitivity or aversion to lavender, peppermint, ginger, or jojoba oils
  • Uncontrolled respiratory conditions such as asthma or COPD
  • Mental incapacitation preventing ability to follow directions
  • Uncontrolled active psychiatric conditions that interfere with study participation
  • Self-reported abnormal smell abilities (e.g., sinus infections, long COVID)
  • Used aromatherapy in the last 30 days

AI-Screening

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Trial Site Locations

Total: 2 locations

1

City of Hope Medical Center

Duarte, California, United States, 91010

Actively Recruiting

2

City of Hope at Irvine Lennar

Irvine, California, United States, 92618

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

4

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