Sticker Pad Containing Essential Oil in Volunteer With High Blood Pressure
- Conditions
- High Blood Pressure
- Interventions
- Device: Sticker pads containing lavender and ylang ylang oilDevice: Placebo
- Registration Number
- NCT05808556
- Lead Sponsor
- Chulalongkorn University
- Brief Summary
The aims of the study were to evaluate efficacy and safety of the sticker pads containing lavender and ylang ylang oil in high blood pressure volunteers
- Detailed Description
High blood pressure volunteers were divided into the sticker group or the placebo group. The volunteers attached the pad to their shirt for 3, 7, 10, and 14 days. Blood pressure, pulse rate, adverse reactions, and satisfaction were investigated.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 34
- age more than 18 years
- systolic blood pressure of more than 130 mmHg but less than 160 mmHg or diastolic blood pressure more than 80 mmHg but less than 100 mmHg
- no hypertensive medicine
- no dermatological diseases, immunocompromised diseases, seizures, asthma, or respiratory diseases
- an unstable condition of other diseases
- olfactory problems
- pregnancy
- lactation
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Sticker pads containing lavender and ylang ylang oil Sticker pads containing lavender and ylang ylang oil The subjects in the sticker pad group attached an sticker pad (0.3% lavender oil and 0.7% ylang ylang oil) to their shirt, close to the right side of the neck, for 14 days Placebo group Placebo The placebo group attached a sticker pad without lavender and ylang ylang oil to their shirt, close to the right side of the neck, for 14 days.
- Primary Outcome Measures
Name Time Method Pulse rate 14 days Measure pulse rate in beats/minutes
Systolic blood pressure 14 days Measure systolic blood pressure in mmHg
Diastolic blood pressure 14 days Measure diastolic blood pressure in mmHg
- Secondary Outcome Measures
Name Time Method adverse reactions of the respiratory tract, skin, gastrointestinal tract, eye, and central nervous system 14 days Using a score of 0 to 3, following an increase of severity
Satisfaction of the product 14 days Using a visual analogue scale, 0 means not satisfied, 10 means very satisfied
Trial Locations
- Locations (1)
Chulalongkorn Hospital
🇹🇭Bangkok, Thailand