- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02163369
The Use of Aromatherapy for Symptom Management
The purpose of this pilot study is to introduce the use of aromatherapy/essential oils to medical oncology patients at Central DuPage Hospital to assess their perceived effectiveness to relieve symptoms of nausea or vomiting and/or anxiety.
Peppermint oil will be used for nausea/vomiting and lavender oil will be used for anxiety. This study will involve administration of aromatherapy to a convenience sample of patients, who will then be asked to complete a brief questionnaire. The questionnaire will involve a simple likert scale to measure efficacy (in the opinion of the patient) and simple multiple-choice questions to determine patients' likeliness to use aromatherapy again.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Mary Lyons, MSN, APN/CNS, RN-BC, ONC
- Phone Number: 630-933-6011
- Email: mary.lyons@cadencehealth.org
Study Contact Backup
- Name: Lorraine Mack, MSN, RN, CNL, OCN
- Phone Number: 630-933-3413
- Email: lorraine.mack@cadencehealth.org
Study Locations
-
-
Illinois
-
Winfield, Illinois, United States, 60190
- Recruiting
- Central DuPage Hospital
-
Contact:
- Mary Lyons, MSN, APN/CNS, RN-BC ONC
- Phone Number: 630-933-6011
-
Contact:
- Lorraine Mack, RN
- Phone Number: 630-933-3413
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Adult hospitalized medical oncology patients admitted to Central DuPage Hospital.
- Age 18 years or greater.
- Able to understand and speak English.
- Women of non-childbearing potential or with childbearing potential with a negative pregnancy test documented during the hospital stay.
- Able to understand concept of aromatherapy for treatment of distressing symptoms.
Exclusion Criteria:
- Prisoners.
- Non-English speaking patients.
- Under the age of 18.
- Unable to comprehend the concept of aromatherapy.
- Severe cognitive impairment.
- Not experiencing the symptoms of nausea, vomiting or anxiety.
- Women with child-bearing potential who have not had a negative pregnancy test during the hospital stay.
- Patients with known allergy to lavender or peppermint.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Peppermint and Lavender Essential Oils
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Post Intervention Patient Interview Form
Time Frame: 24hrs post aromatherapy
|
24hrs post aromatherapy
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Mary Lyons, MSN, APN/CNS, RN-BC, ONC, Central DuPage Hospital
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 14-031-1
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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