Actively Recruiting
Aromatherapy Inhaler Use for HSCT Distress
Led by Stanford University · Updated on 2026-04-13
50
Participants Needed
1
Research Sites
50 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this research is to evaluate aromatherapy inhaler use and how it may impact cancer distress and coping by patients in the first few days after hematopoietic stem cell transplant (HSCT).
CONDITIONS
Official Title
Aromatherapy Inhaler Use for HSCT Distress
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Autologous and Allogeneic patients admitted to E1 for planned HSCT
- Patients with hematologic malignancies requiring HSCT
- No allergies to lavender or peppermint essential oils
- Must have received chemotherapy during preparative regimen (single or multi-agent regimen)
- Adult patient over 18 years of age
- Able to speak, read, and comprehend English
- Willing and capable of providing informed consent
You will not qualify if you...
- Patients admitted for Chimeric Antigen Receptor T cell (CART) infusion
- Patients receiving a transplant for a germ cell tumor diagnosis
- Unexpected or unplanned admission (e.g., neutropenic fever, confusion, clinical deterioration)
- Immune effector cell-associated neurotoxicity syndrome (ICANS) grade 1 through 4
- History of scleroderma
- History of atrial fibrillation
- Known history of G6PD deficiency
- Allergic to lavender or peppermint essential oils
- Pediatric patient 18 years of age or less
- Unable to speak, read, and comprehend English
- Unwilling or incapable of providing informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Stanford University
Stanford, California, United States, 94305
Actively Recruiting
Research Team
A
Aubrey Florom-Smith, PhD, RN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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