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Clinical Trials/NCT03090750
NCT03090750
Completed
Phase 1

What is the Effect of Using Aromatherapy to Reduce Anxiety in Patients Undergoing Invasive Radiologic Procedures?

Wake Forest University Health Sciences0 sites31 target enrollmentJuly 16, 2015

Overview

Phase
Phase 1
Intervention
Lavender Oil
Conditions
Anxiety
Sponsor
Wake Forest University Health Sciences
Enrollment
31
Primary Endpoint
Anxiety level of patients
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The purpose of this study is to see if using aromatherapy (Lavender or Bergamot) will lower anxiety in patients having invasive Radiology procedures. First, the level of anxiety is assessed prior to the procedure using a questionnaire. Then, patients are given the aromatherapy treatment during the pre-procedure period. Then, the same questions are asked to determine how anxious the patient is after the aromatherapy and before going into the procedure room. After the procedure, patients are asked to evaluate the process of the study.

Registry
clinicaltrials.gov
Start Date
July 16, 2015
End Date
March 2017
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Scheduled for Myelogram or IR invasive procedure at investigative site

Exclusion Criteria

  • Incapable of giving informed consent
  • Requiring pre-medication for scheduled procedure
  • Allergy to lavender or bergamot
  • Asthma (type of breathing related condition)
  • COPD (Chronic Obstructive Pulmonary Disorder - breathing disease)
  • Respiratory issues requiring oxygen therapy

Arms & Interventions

Lavender

Lavender oil

Intervention: Lavender Oil

Bergamot

Bergamot oil

Intervention: Bergamot Oil

Water

Water

Intervention: Water

Outcomes

Primary Outcomes

Anxiety level of patients

Time Frame: Immediately prior to invasive radiologic procedure

Assessed with Amsterdam Preoperative Anxiety and Information Scale

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