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The Effects of Smell on Mood and Physical Responses

National Institutes of Health (NIH) logo

National Institutes of Health (NIH)

Status and phase

Completed
Phase 1

Conditions

Depression
Anxiety
Stress

Treatments

Behavioral: Exposure to relaxant and stimulant odors

Study type

Interventional

Funder types

NIH

Identifiers

NCT00097253
R21AT002122-01

Details and patient eligibility

About

The purpose of this study is to examine the body's response to relaxing and stimulating fragrances commonly used in aromatherapy.

Full description

Despite aromatherapy's popularity, efficacy data are scant, and potential mechanisms are controversial. This randomized controlled trial examined the psychological, autonomic, endocrine, and immune consequences of one purported relaxant odor (lavender), one stimulant odor (lemon), and a no-odor control (water), before and after a stressor (cold pressor); 56 healthy men and women were exposed to each of the odors during three separate visits. To assess the effects of expectancies, participants randomized to the "blind" condition were given no information about the odors they would smell; "primed" individuals were told what odors they would smell during the session, and what changes to expect. Experimenters were blind.

In each case we measured several different aspects of the cellular immune response, as well as skin barrier repair following tape stripping. This design allowed us to examine the ability of the odors to modulate endocrine and immune function, and health-relevant cutaneous responses.

Enrollment

56 patients

Sex

All

Ages

18 to 44 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy adults with a normal sense of smell

Exclusion criteria

  • Treatment with medication that has immunological or endocrinological consequences
  • Chronic health problems that affect immune or endocrine systems
  • Allergy to perfume or cosmetics
  • Problems with sense of smell
  • Respiratory problems
  • Smoker
  • Current active asthma
  • Use of psychoactive drugs or mood-altering medication
  • History of anxiety disorder, major depression, bipolar disorder, schizophrenia, or other psychotic disorders
  • History of chest pain or ventricular fibrillation

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

56 participants in 3 patient groups, including a placebo group

Lavender
Experimental group
Treatment:
Behavioral: Exposure to relaxant and stimulant odors
Citrus
Experimental group
Treatment:
Behavioral: Exposure to relaxant and stimulant odors
Water
Placebo Comparator group
Treatment:
Behavioral: Exposure to relaxant and stimulant odors

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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