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Phase 1 N=56 Randomized Double-blind Treatment

The Effects of Smell on Mood and Physical Responses

Stress · Anxiety · Depression

Enrolled (actual)
56
Serious AEs
0.0%
Results posted
Feb 2010
Primary outcome: Primary: Cortisol and Catecholamine Production — 0.107; 0.119; 0.107; 43.5 pg/ml (log 10) — p=0.83

Study Design & Population

Study type
Interventional
Phase
Phase 1
Interventions
Exposure to relaxant and stimulant odors (Behavioral)
Age
Adult · 18+ yrs
Sex
All
Sponsor
National Center for Complementary and Integrative Health (NCCIH)
Primary completion
Mar 2006

Outcome Measures

OutcomeResultp-value
PRIMARY
Cortisol and Catecholamine Production
0.107; 0.119; 0.107; 43.5; 44.3; 38.3 0.83
PRIMARY
Immune Function
3.706; 3.622; 3.623; 1.777; 1.734; 1.787 0.10
PRIMARY
Skin Barrier Repair
23.21; 24.33; 22.11; 15.64; 17.78; 16.82 0.60
PRIMARY
Immune Function: Delayed Hypersensitivity to Candida(DTH)
10.84; 17.39; 12.40 0.014 sig

Summary

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

Eligibility Criteria

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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00097253). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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