Comparison of the effect of oral capsule and aroma of lavender on the quality of sleep in perimenopausal wome

Early Phase 1

Recruiting

• Conditions: Sleep.; Insufficient sleep syndrome; F51.12

• Registration Number: IRCT20151228025732N47
• Lead Sponsor: Semnan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 30

Inclusion Criteria

Women aged 39-51 in transient menopausal period
Healthy sense of smell
No taking sleeping pills during the last month

Exclusion Criteria

Drug addiction
History of mental disorders
History of asthma, bronchitis, chronic respiratory diseases

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Sleep Quality. Timepoint: Before intervention and after intervention (one month later). Method of measurement: PSQI- Pittsburgh Sleep Quality Index.