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The effect aromatherapy with lavender on sleep quality third trimester pregnant women referred to Fatemieh hospital in Hamadan in 2016

The effect aromatherapy with lavender on sleep quality third trimester pregnant women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016061710426N11
Enrollment
72
Registered
2016-06-28
Start date
2016-07-01
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aromatherapy with lavender on sleep quality in pregnancy

Interventions

Intervention 1: Intervention: After obtaining written testimonial from samples, People who score high of 5 in the questionnaire, Coincidentally divided with the lottery with a coin into one of two gr
Treatment - Drugs
Placebo
Intervention: After obtaining written testimonial from samples, People who score high of 5 in the questionnaire, Coincidentally divided with the lottery with a coin into one of two groups of experim
Control : . Mothers in the control group to be delivered placebo (water) in a bottle as same as intervention group.Mothers will ask for a a month, four days a week at night before going to bed two

Sponsors

Hamadan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age ranged between 18-35 years; primi- gravid; lack of lavender mother's insensitivity; lack of physical and mental illness in the mother; lack of stress and domestic violence against the mother; the absence of high-risk pregnancy symptoms in the mother; No history of allergic rhinitis; eczema or breathing problems such as asthma ;lack of drug addiction. Exclusion criteria:The incidence of allergy symptoms in the mother, lavender inhaled less than four times a week.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sleep quality. Timepoint: before, two weeks after intervention-four weeks after intervention. Method of measurement: Standard Pittsburgh Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Parisa Parsa

Hamadan University of Medical Sciences

parsa@umsha.ac.ir+98 81 3838 0150

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026