Inhaled Essential Oil Effect on Common QOL Concerns During Cancer Treatment

Sponsor

Ohio State University Comprehensive Cancer Center (Other)

Overall Status

Completed

CT.gov ID

NCT03858855

Collaborator

(none)

248

Enrollment

Location

Arms

13.8

Actual Duration (Months)

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This single-blind, randomized controlled trial studies how well inhaled essential oils work for common quality of life concerns in patients who are undergoing cancer treatment such as chemotherapy, targeted therapy, and/or immunotherapy given through the vein (intravenously). Aromatherapy using essential oils, such as ginger essential oil, German chamomile essential oil, and bergamot essential oil, may improve quality of life issues such as nausea, anxiety, loss of appetite, and fatigue in patients undergoing treatment for cancer.

Condition or Disease	Intervention/Treatment	Phase
Gastrointestinal Cancer Neuroendocrine Carcinoma Skin Cancer	Procedure: Aromatherapy and Essential Oils Procedure: Aromatherapy and Essential Oils Procedure: Aromatherapy and Essential Oils Procedure: Aromatherapy and Essential Oils Other: Subject Diary	N/A

Detailed Description

PRIMARY OBJECTIVES:

To determine if aromatherapy, specifically inhaled essential oil, is beneficial for side effects related to cancer treatments involving chemotherapy, targeted therapy, and/or immunotherapy administered intravenously.
To describe the effect of inhaled ginger essential oil, German chamomile essential oil, and bergamot essential oil on nausea and anxiety of patients receiving chemotherapy, targeted therapy, and/or immunotherapy administered intravenously.
To describe the effect of decreased levels of nausea and/or anxiety on levels of appetite and/or fatigue.
To evaluate the acceptability of using a personal inhalation bottle for inhalation of essential oils.

OUTLINE: Patients are randomized to 1 of 4 groups.

GROUP I: Patients inhale 7 drops of bergamot essential oil using a personalized inhalation bottle three times daily (TID) (morning, midday, and evening) for up to 7 days. Patients also use a journal to document symptoms, time of inhalation, and medication use TID for up to 7 days.

GROUP II: Patients inhale 7 drops of chamomile essential oil and complete journal as in group I.

GROUP III: Patients inhale 7 drops of ginger essential oil and complete journal as in group I.

GROUP IV (CONTROL): Patients inhale 7 drops of almond essential oil and complete journal as in group I.

Study Design

Study Type:

Interventional

Actual Enrollment :

248 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

Single (Participant)

Primary Purpose:

Supportive Care

Official Title:

Inhaled Essential Oil Effect on Common Quality of Life Concerns During Cancer Treatment

Actual Study Start Date :

Feb 18, 2019

Actual Primary Completion Date :

Apr 13, 2020

Actual Study Completion Date :

Apr 13, 2020

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Group I (bergamot essential oil) Patients inhale 7 drops of bergamot essential oil using an essential oil administration bottle TID (morning, midday, and evening) for up to 7 days. Patients also use a journal to document symptoms, time of inhalation, and medication use TID for up to 7 days.	Procedure: Aromatherapy and Essential Oils Use bergamot essential oil Other Names: Aromatherapy Other: Subject Diary Complete journal Other Names: Patient Diary Subj Diary Form Subject Diary Form
Experimental: Group II (chamomile essential oil) Patients inhale 7 drops of chamomile essential oil and complete journal as in group I.	Procedure: Aromatherapy and Essential Oils Use chamomile essential oil Other Names: Aromatherapy Other: Subject Diary Complete journal Other Names: Patient Diary Subj Diary Form Subject Diary Form
Experimental: Group III (ginger essential oil) Patients inhale 7 drops of ginger essential oil and complete journal as in group I.	Procedure: Aromatherapy and Essential Oils Use ginger essential oil Other Names: Aromatherapy Other: Subject Diary Complete journal Other Names: Patient Diary Subj Diary Form Subject Diary Form
Active Comparator: Group IV (almond essential oil) Patients inhale 7 drops of almond essential oil and complete journal as in group I.	Procedure: Aromatherapy and Essential Oils Use almond essential oil Other Names: Aromatherapy Other: Subject Diary Complete journal Other Names: Patient Diary Subj Diary Form Subject Diary Form

Outcome Measures

Primary Outcome Measures

Effects of essential oils on nausea and anxiety [Up to 7 days]
Levels of nausea and anxiety will be measured using a numerical grading scale of 0-10. 0 will equal "good" meaning no nausea or anxiety. 10 will equal "horrible" meaning the worst nausea or anxiety. Data for each outcome will be collected 3 times a day, for a total of 21 measurements from each subject. For data analysis, we will compress the 21 measures into 3 scores. Each subject will be given a daily outcome level by averaging the 3 measures. The 7 daily outcome levels will become 3 scores by averaging data from days 1 and 2 (Period 1), days 3 and 4 (Period 2), and days 5, 6, and 7 (Period 3). Using the 3 scores, each outcome will be modeled using a repeated measures regression allowing the variability of outcome scores to vary with period. Period, group membership, the interaction between period and group membership, gender, age, and type of cancer will be model predictors. For each outcome, the contrast of interest will be that between each treatment group and the control group.

Secondary Outcome Measures

Determine if decreased levels of nausea and/or anxiety effect appetite and/or fatigue [Up to 7 days]
Anticipated results of the study are that patients will report decreased levels of nausea and anxiety. With the decreased levels of nausea and anxiety, we anticipate that patients will report increased levels of appetite and decreased levels of fatigue. Loss of appetite and fatigue will be measured using a numerical grading scale of 0-10. 0 will equal "good" meaning no loss of appetite or fatigue. 10 will equal "horrible" meaning the worst appetite loss or fatigue. Data will be collected, measured, and analyzed in the same manner as Outcome 1.
Acceptability of using a personal inhalation bottle for inhalation of essential oils - ease of use [Up to 7 days]
The overall ease of using the personal inhalation bottle will be measured through post-study ratings by participants. A numerical rating scale of 1-5 will be used. 1 will equal strongly disagree; 2 will equal disagree; 3 will equal neither agree nor disagree; 4 will equal agree; and 5 will equal strongly agree. The study will compare via a percentage those participants with positive acceptability when compared to those with negative acceptability.
Acceptability of using a personal inhalation bottle for inhalation of essential oils - utilization post study period [Up to 7 days]
The utilization of the personal inhalation bottle beyond the study period will be measured through post-study ratings by participants. A numerical rating scale of 1-5 will be used. 1 will equal strongly disagree; 2 will equal disagree; 3 will equal neither agree nor disagree; 4 will equal agree; and 5 will equal strongly agree. The study will compare via a percentage those participants with positive acceptability when compared to those with negative acceptability.
Acceptability of using a personal inhalation bottle for inhalation of essential oils - perception of benefit of essential oil for symptoms [Up to 7 days]
The overall perception of help for symptoms will be measured through post-study ratings by participants. A numerical rating scale of 1-5 will be used. 1 will equal strongly disagree; 2 will equal disagree; 3 will equal neither agree nor disagree; 4 will equal agree; and 5 will equal strongly agree. The study will compare via a percentage those participants with positive acceptability when compared to those with negative acceptability.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Gastrointestinal cancers, neuroendocrine cancer, or melanoma or other skin cancers
Receiving chemotherapy, targeted therapy, and/or immunotherapy
Not naive to the treatment
Must be able to read and write English

Exclusion Criteria:

Allergies to ragweed, chrysanthemum, chamomile, ginger, bergamot, citrus fruits, tree nuts, perfumes
Asthma diagnosis
Patients receiving only octreotide injections
Patients receiving floxuridine (FUDR) via hepatic artery infusion (HAI) pump only