Investigation on the effectiveness inhalation aromatherapy with Lavender essential oil versus placebo on the anxiety of patients with burns. a double blinded randomized clinical trial

Phase 2

Conditions: Condition 1: Burns. Condition 2: Anxiety.
Burns involving 20-29% of body surface, Burns involving 30-39% of body surface, Burns involving 40-49% of body surface, Burns involving 50-59% of body surface, Burns involving 60-69% of body surface
Any other mood disorders that do not justify classification to F30-F34, because they are not of sufficient severity or duration
T31.2, T31

Registration Number: IRCT2013042413110N1

Lead Sponsor: Vice-Chancellor of Education and Research Arak University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Complete

Sex: All

Target Recruitment: 60

Inclusion Criteria

age 18 to 65 years; burns degree of 2 or 2 and 3 with 15 to 60 percent burn level; stability of hemodynamic status; lack of inhalation burns; lack of allergy or respiratory diseases; lack of narcotic addiction or drug abuse. Exclusion criteria: Lack of patient cooperation during the intervention for any reason; creation dangerous conditions of disease during the intervention; allergy to inhalation of Lavender Essential Oil during the intervention.

Exclusion Criteria

Not provided

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Anxiety. Timepoint: Before and 20 minutes after inhalation of lavender (experimental group) or distilled water (control group) for three consecutive nights. Method of measurement: Spielberger questionnaire.

Secondary Outcome Measures