AroMatherapy for Blood and Marrow Transplant PatIENTs (AMBIENT)
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Hackensack Meridian Health
- Enrollment
- 30
- Locations
- 2
- Primary Endpoint
- Using the Halpin 0-to-5 Nausea and Vomiting Scales to document the degree of severity of patients' self-reported blood and marrow transplant conditioning regimen induced nausea and vomiting
Study Overview
Brief Summary
The study is comparing the difference between the use of Elequil Aromatabs versus standard of care practice treatments on Blood Marrow Transplantation patients.
Detailed Description
The primary objective is to examine whether there are differences in the level of anxiety and nausea between patients in the treatment and control groups.
The secondary objective is to compare the number of as needed (PRN) antiemetics and anxiolytics, as well as the duration of prolonged standardized antiemetic and anxiolytic regimen for the treatment and control cohorts.
The sample size of 200 patients is anticipated to be enrolled over a period of 1 year. A total of 50 patients will be enrolled in each of the four groups The enrollment procedure will begin with a screening of patients who are admitted within 24 hours of admission for blood and marrow transplantation conditioning to evaluate if they meet the inclusion criteria. Patients who meet inclusion criteria will be offered an opportunity to participate in the study.
The patient will complete an informed consent form, then assessed to identify their predominant symptom:anxiety or nausea. Based on the patients' primary symptom, they will be randomized into either control or treatment group for a total of four groups (nausea treatment, nausea control, anxiety treatment, and anxiety control). The study will be using a Wei's Urn algorithm for the randomization sequence. The randomization sequence and patient information will be stored in a protected SharePoint folder between the 8PE and 8PW nurses enrolled with the Institutional Review Board as study staff.
Patients enrolled in the nausea control/treatment group will be required to complete a Generalized Anxiety Disorder 7-Item Scale (GAD-7) form to determine the baseline of anxiety.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Masking Description
The patient will be randomly assigned to a group based on their primary symptoms. The RN will be communicating with the patient for assessments, administering medications, and submitting results collected into the EPIC system.
Eligibility Criteria
- Ages
- 22 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Adult blood and marrow transplant patients admitted to 8 Pavilion East Blood and Marrow Transplant and 8 Pavilion West Blood and Marrow Transplant for autologous and allogeneic blood and marrow transplant conditioning (chemotherapy and/or radiation therapy) and transplant cell infusion
- •Ages 22 and above. Adults ages 18-21 are admitted under the pediatric service and are not admitted to 8PE and 8PW
- •Patients with blood and marrow transplant conditioning induced nausea and vomiting-
- •Patients expressing feeling of anxiety
- •English and Spanish speaking only
- •Patients enrolled in other research studies that allow them to participate
Exclusion Criteria
- •Patients with known allergy to lavender
- •Patient with known allergy to orange/peppermint
- •Patients less than 22 years
- •Patients with olfactory/sinus impairment
- •Patients unable to give written informed consent
- •Patients admitted for inpatient conditioning but receiving transplant cell infusion in the outpatient setting
Outcomes
Primary Outcomes
Using the Halpin 0-to-5 Nausea and Vomiting Scales to document the degree of severity of patients' self-reported blood and marrow transplant conditioning regimen induced nausea and vomiting
Time Frame: 12-hour intervals for a year
Differences in the severity of nausea and vomiting between patients in the treatment and control groups
Using the Patient Self-Report of Anxiety Assessment Tool to document the degree of severity of patients' self-reported anxiety
Time Frame: 12-hour intervals for a year
Differences in the severity of anxiety between patients in the treatment and control groups
Secondary Outcomes
- Number of PRN antiemetics for prolonged standardized antiemetic regimen(1 year)
- Number of PRN anxiolytics for prolonged standardized anxiolytic regimen(1 year)
- Duration of PRN anxiolytics for prolonged standardized anxiolytic regimen(1 year)
- Using the Halpin 0-to-5 Nausea and Vomiting Scales to document the severity of nausea/vomiting prior to and following application of the patch(one hour prior to and following application of the patch)
- Duration of PRN antiemetics for prolonged standardized antiemetic regimen(1 year)
- Using the Patient Self-Report of Anxiety Assessment Tool to document the severity of anxiety prior to and following application of the patch(one hour prior to and following application of the patch)