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Comparing the effect of aromatherapy on sleep quality and insomnia severity in patients with breast cancer

Comparison of the effect of aromatherapy with Citrus aurantium and chamomile extracts on sleep quality, insomnia severity in breast cancer patients undergoing chemotherapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171013036747N4
Enrollment
186
Registered
2025-08-04
Start date
2025-08-21
Completion date
Unknown
Last updated
2025-08-19

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

Conditions

Condition 1: Cancer. Condition 2: Sleep disorders. Personal history of malignant neoplasms of other organs and systems Sleep disorders

Interventions

Intervention 1: Intervention group 1: Chamomile essential oil from Oil Darou Company
At 10 pm, the patient inhales 5 deep breaths for 10 minutes at equal intervals, and a handkerchief soaked in essential oil that will emit the scent for at least 8 hours is attached to the front of the
At 10 pm, the patient inhales the essential oil by taking 5 deep breaths for 10 minutes at equal intervals, and a handkerchief soaked in the essential oil that will emit the aroma for at least 8 hours

Sponsors

Birjand University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: A lack of stressful events such as near-death or surgery in the last six months Age range from 18 to 60 years Having the consent to participate in the study Do not use the herbal remedy in the past month Not having allergic rhinitis, asthma, chronic pulmonary disease, sleep disorders and other chronic diseases that affect the sense of smell Lack of susceptibility to medicinal herbs Lack of sleeping pills Having breast cancer Patients undergoing chemotherapy (in the second to fourth cycles of chemotherapy)

Exclusion criteria

Exclusion criteria: Occurrence of stressful events: close lives, divorces and ... during the study Use sleep Palliative interventions during the study Symptoms of allergy to the fragrance used

Design outcomes

Primary

MeasureTime frame
Sleep quality. Timepoint: Before and 7 days after the intervention. Method of measurement: Standard sleep quality questionnaire Pittsburgh.;Insomnia intensity. Timepoint: Before and 7 days after the intervention. Method of measurement: Standard sleep quality questionnaire Pittsburgh.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRasool Solaimani Moghaddam

Birjand University of Medical Sciences

Rasool.solaimani@yahoo.com+98 56 3238 1200

Outcome results

None listed

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