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Comparing the effects of aromatherapy and music therapy on preoperative anxiety

A comparative study of the effect of aromatherapy and music therapy on physiological indices and preoperative anxiety of mastectomy candidates

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230221057482N1
Enrollment
99
Registered
2023-02-28
Start date
2023-04-03
Completion date
Unknown
Last updated
2023-03-13

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

Conditions

Breast Cancer. Malignant neoplasm of breast

Interventions

Intervention 1: First intervention group: Aromatherapy
The aims and methods of this study will be explained to all eligible patients at the beginning of the study. Next, the researcher will complete the demographic and clinical characteristics questionnai

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Consent to participate in the study Female sex 18 to 65 years old age Stage 3 or 4 of breast cancer Performing surgery for the first time Having surgery on the same day Anxiety score of 5 or higher according to the NVAAS tool Not using sedatives and painkillers (at least in the last 24 hours) Not using drugs or corticosteroid products and other central nervous and endocrine system affecting drugs (according to medical records) Having a mental health condition Literacy in Persian reading and writing

Exclusion criteria

Exclusion criteria: Olfactory dysfunction (for the aromatherapy group) Auditory impairment (for the music therapy group) Visual impairment (to measure anxiety using the NVAAS scale) History of allergies, eczema and respiratory diseases Reluctance and disinterest in listening to music Reluctance and disinterest in aromatherapy and rose essential oil

Design outcomes

Primary

MeasureTime frame
Anxiety score on the numerical visual analogue anxiety scale. Timepoint: At the beginning of the study and 10 minutes after the intervention has ended. Method of measurement: Numerical Visual Analogue Anxiety Scale.

Secondary

MeasureTime frame
Physiological indices (systolic and diastolic blood pressure, heart rate, respiratory rate, arterial blood oxygen saturation and salivary cortisol level). Timepoint: At the beginning of the study and 10 minutes after the intervention has ended. Method of measurement: Monitor device, pulse oximetry, laboratory kit (by ELISA method).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFaezeh Samadi

Tehran University of Medical Sciences

f-samadi@razi.tums.ir+98 21 8474 2616

Outcome results

None listed

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