Effects of Aromatherapy on Patients Undergoing Chemotherapy for Breast Cancer
- Conditions
- Sleep QualityAnxiety
- Interventions
- Other: AromatherapyOther: No intervention
- Registration Number
- NCT06338527
- Lead Sponsor
- Weifang Medical University
- Brief Summary
The objective of this study was to investigate the effects of aromatherapy on sleep quality and anxiety in patients undergoing chemotherapy for breast cancer.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 90
- patients diagnosed with breast cancer and receiving chemotherapy; 2) suffering from sleep disorders or PSQI score greater than 5; 3) not using medications such as antidepressants and hypnotics that may affect the observation results; 4) age older than 18 years and volunteered to participate in this study.
- Asthma or severe respiratory disease; 2) Allergy to lavender; 3) Cognitive or communication disorders; 4) Breast cancer combined with severe organ dysfunction.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Experimental group Aromatherapy The researchers placed 2 drops of lavender oil on gauze in a box each night 30 minutes before the patient went to bed and placed it 15 to 20 centimeters from the pillow. Control group No intervention The control group had no aromatherapy intervention during the study period.
- Primary Outcome Measures
Name Time Method Sleep quality The sleep quality of the patients was assessed at 8 a.m. for one week. The Pittsburgh Sleep Quality Index (PSQI) was used to assess the sleeping quality of the patients. The total score of PSQI ranged from 0-21, with higher scores indicating poor sleep quality.
Anxiety The anxiety level of the patients was assessed at 8 a.m. for one week. Beck Anxiety Inventory (BAI) was used to assess the anxiety level of the patients. The scale consists of 21 entries with a total score ranging from 0 to 63, with higher total scores being associated with more severe levels of anxiety.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Weifang People's Hospital
🇨🇳Weifang, Shangdong, China