Using lavender aromatherapy to reduce anxiety during skin cancer surgery
Effects of Lavender Aromatherapy on Patient Anxiety During Mohs Micrographic Surgery
This study tests if breathing in lavender scent can help reduce anxiety and improve comfort for patients having skin cancer surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Case Comprehensive Cancer Center Academic / other |
| Locations | 1 site (Cleveland, Ohio) |
| Trial ID | NCT06167096 on ClinicalTrials.gov |
What this trial studies
This study explores the effects of lavender aromatherapy on reducing anxiety and unpleasant odor perception in patients undergoing Mohs Micrographic Surgery (MMS) for skin cancer. By utilizing lavender's known calming properties, the research aims to enhance patient comfort and experience during this anxiety-inducing procedure. The study will assess the impact of inhaling lavender aroma on anxiety levels and overall satisfaction with the surgical process, providing insights into non-pharmacological interventions for patient care.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who are scheduled for Mohs surgery of the head and neck at the University Hospitals Westlake Dermatology Clinic.
Not a fit: Patients with allergies to lavender, aroma sensitivities, anosmia, or current cold or flu symptoms may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve patient comfort and reduce anxiety during skin cancer surgeries.
How similar studies have performed: Previous studies have shown promising results for lavender aromatherapy in reducing anxiety in various medical settings, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * At least 18 years of age * No previous Mohs surgeries * Currently seen in UH(University Hospitals)Westlake Dermatology Clinic for Mohs surgery * Mohs surgery of the head and neck Exclusion Criteria: * Participants with lavender allergies * Participants with aroma sensitivities * Participants with anosmia * Participants with cold or flu symptoms
Where this trial is running
Cleveland, Ohio
- University Hospitals Cleveland Medical Center, Seidman Cancer Center, Case Comprehensive Cancer Center — Cleveland, Ohio, United States (Recruiting)
Study contacts
- Principal investigator: Bryan Carroll, MD, PhD — University Hospitals Cleveland Medical Center, Case Comprehensive Cancer Center
- Study coordinator: Bryan Carroll, MD, PhD
- Email: Bryan.Carroll@uhhospitals.org
- Phone: 216-844-7834
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.