Effects of Lavender Aromatherapy on Patient Anxiety During Mohs Micrographic Surgery (NCT06167096) | Clinical Trial Compass
CompletedNot Applicable
Effects of Lavender Aromatherapy on Patient Anxiety During Mohs Micrographic Surgery
United States89 participantsStarted 2024-07-24
Plain-language summary
This study aims to improve patient comfort by exploring the potential of lavender aromatherapy in reducing anxiety and unpleasant odor perception during Mohs Micrographic Surgery (MMS).
Lavender has been widely studied for its sedative-like properties and calming effects, both in medical and dental settings. By investigating the impact of lavender aromatherapy on patient anxiety levels during MMS, we seek to provide evidence-based insights into non- pharmacological interventions that can enhance the overall comfort and experience of participants.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Change in participant anxiety levels as measured by STAI assessment scale
Timeframe: Before MMS procedure
2
Change in participant anxiety levels as measured by STAI assessment scale
Timeframe: After MMS procedure post 1 layer
3
Change in participant anxiety levels as measured by VAS assessment scale
Timeframe: Before MMS procedure
4
Change in participant anxiety levels as measured by VAS assessment scale