Actively Recruiting
Evaluating Aromatherapy with Asian Plant Extracts to Reduce Distress in Breast Cancer Patients Before Radiotherapy
Led by National Cancer Centre, Singapore · Updated on 2025-01-09
300
Participants Needed
1
Research Sites
101 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating the use of inhalation aromatherapy as a complementary therapy to reduce distress in female breast cancer patients in Singapore who are scheduled to begin radiotherapy. The study focuses on the effects of inhaling extracts from familiar Asian aromatic plants and aims to establish evidence for aromatherapy's role in cancer care. This research involves a randomized, double-blind design comparing the intervention to a placebo control. Participants will be randomly assigned to one of two groups: one group receives an inhaler stick with 2 drops of an Asian plant extract blend, while the other group receives a placebo inhaler with 2 drops of carrier oil. On the day of their first radiotherapy session, patients will use the inhaler by holding it about 8 cm from their nose and taking up to three sniffs every 5 minutes for a total of 20 minutes. This inhalation procedure is designed to assess aromatherapy's impact on distress and anxiety. During the study, patients will undergo evaluations including distress and anxiety scoring, blood pressure and pulse rate measurements, and saliva sample collection before and after the inhalation intervention. These measures will be repeated at baseline on the day of CT simulation and on the radiotherapy day before and after the intervention. The study plans to recruit 300 breast cancer patients aged 21 to 99 years, monitoring outcomes related to distress, anxiety, and cortisol levels associated with stress.
CONDITIONS
Official Title
Evaluating the Effectiveness of Aromatherapy for Alleviating Distress in Breast Cancer Patients Before Radiotherapy.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 21 years old and above
- Confirmed diagnosis of breast cancer of any stage
- Scheduled to undergo radiotherapy for the first time
- Capable of providing informed consent
You will not qualify if you...
- Physically or mentally incapable of providing verbal/written consent
- Known or suspected hypersensitivity/allergy to essential oils or any components of the formulations
- Airway hypersensitivity to fragrances, paint fumes or turpentine
- Taking medications for anxiety (e.g. benzodiazepines) before radiotherapy
- Pregnant, breastfeeding, or intending to conceive during study period
AI-Screening
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Trial Site Locations
Total: 1 location
1
National Cancer Centre Singapore
Singapore, Singapore, 168583
Actively Recruiting
Research Team
D
Dr. Fuh-Yong Wong, MBBS, FRCR
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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