Aromatherapy effect on sleep quality in menopausal women

The effects of Rosa Damascene aromatherapy on sleep quality in menopausal women

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2015111420778N4

Enrollment

Registered

2016-09-02

Start date

2015-12-22

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

Condition 1: Sleep disorder. Condition 2: Menopause. Sleep Disorders Menopausal and other perimenopausal disorders

Interventions

Intervention 1: intervention group: Rosa Damascene fragrance will be used by participants in the intervention group nightly before sleeping. The fragrance will be dropped on cotton balls, which were

which will be completed at the baseline

fourth

and eighth weeks after the intervention. Data Will be analyzed using independent t test and repeated measures analysis of variance calculated by SPSS 16. Intervention 2: Control group: no interventio

Treatment - Drugs

intervention group: Rosa Damascene fragrance will be used by participants in the intervention group nightly before sleeping. The fragrance will be dropped on cotton balls, which were placed on a cy

and eighth weeks after the intervention. Data Will be analyzed using independent t test and repeated measures analysis of variance calculated by SPSS 16.

Control group: no intervention will be performed in this group.

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Consent to participate in the project; Passing at least one year from the last menstrual period; confirmed menopause; women without diabetes; hypertension; heart and respiratory disease; consumption sleep pills; hormone replacement therapy; mental disorders and Pittsburgh Sleep Quality Index score of 5 or above. Exclusion criteria: Dissatisfaction to participant in the study; Allergic signs and symptoms while taking aromatherapy; use Rose less than 4 times a week; detection of diabetes and hypertension during intervention; any major stressors.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Improve of sleep quality. Timepoint: Before intervention 6 weeks after intervention and 4 weeks after the cessation intervention. Method of measurement: Pittsburgh questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFateme Mogaddam Tabrizi

University of Medical Sciences of urmia

fmtabrizi@gmail.com+98 44 3275 4964

Outcome results

None listed

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