Essential Oil Blend for Anxiety

N/A

Waitlist Available

Led By Jessie Hawkins, PhD

Research Sponsored by Franklin School of Integrative Health Sciences

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up baseline and at 15 minutes

Summary

The purpose of this study is to assess the potential for a non-invasive sensory based intervention to reduce the stress associated with a COVID-19 diagnosis.

Eligible Conditions

Anxiety
Stress
Coronavirus

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ baseline and at 15 minutes

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~baseline and at 15 minutes

This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline and at 15 minutes for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.

Primary study objectives

Change from baseline in mood state on the Abbreviated Profile of Mood States (POMS)

Change from baseline in state anxiety on the State portion of the State Trait Anxiety Scale (STAI-S) at 15 minutes

Trial Design

2Treatment groups

Experimental Treatment

Placebo Group

Group I: InterventionExperimental Treatment1 Intervention

Participants receive an active essential oil blend to inhale for 15 minutes. The blend contains plant based oils sourced from flowers and citrus plants.

Group II: ControlPlacebo Group1 Intervention

Participants receive an inert comparison to inhale for 15 minutes.

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