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Clinical Trials/NCT05910892
NCT05910892
Withdrawn
N/A

The Effect of Aromatherapy on the Incidence and Severity of Post Procedure Pain and Discomfort in Patients

University of Washington0 sites25 target enrollmentJanuary 1, 2025

Overview

Phase
N/A
Intervention
Aromatherapy packet
Conditions
Chronic Pain
Sponsor
University of Washington
Enrollment
25
Primary Endpoint
Change in Acute Pain
Status
Withdrawn
Last Updated
10 months ago

Overview

Brief Summary

Effect of aromatherapy on pain and discomfort in patients who are receiving intramuscular stimulation therapy or trigger point injections for chronic pain.

Detailed Description

The study will explore the effect of aromatherapy on pain and discomfort in patients who are receiving intramuscular stimulation therapy or trigger point injections for chronic pain. This will be a blinded study where patients will act as their own control over two treatment visits. On one visit patient will be exposed to either the aromatherapy or a placebo. On their second visit patients will be exposed to the other compound. The study will collect demographic data, pain intensity and affect, and catastrophizing information.

Registry
clinicaltrials.gov
Start Date
January 1, 2025
End Date
July 1, 2025
Last Updated
10 months ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Heather Tick

Clinical Professor: School of Medicine

University of Washington

Eligibility Criteria

Inclusion Criteria

  • Have received at least one (1) prior IMS or trigger point injection treatment with researcher
  • 18 years of age or older
  • English language speaker
  • has completed Pain Tracker (clinic standard of care) questionnaire prior to study visit
  • any analgesic medication taken must be consistent for both sessions

Exclusion Criteria

  • Non-English language speaker
  • Allergy to essential oils
  • Asthmatic
  • Patient unable to self-administer aromatherapy

Arms & Interventions

Aromatherapy before treatment

Subject receives aromatherapy before IMS treatment or trigger point injection

Intervention: Aromatherapy packet

Placebo before treatment

Subject receives placebo before IMS treatment or trigger point injection

Intervention: Placebo packet

Outcomes

Primary Outcomes

Change in Acute Pain

Time Frame: Immediately after the Procedure

Examine the change in Acute Pain associated with two identical procedures involving muscle with either an aromatherapy intervention or control intervention. With each patient being their own control, patients will rate their acute pain immediately after the procedure on a 0-10 scale (0=No pain and 10=Pain as bad as you can imagine).

Secondary Outcomes

  • Change in Overall Experience(Immediately after the Procedure)

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