The Effectiveness and Safety of Integrative Korean Medicine Treatment for Bell's Palsy
- Conditions
- Facial Paralysis, Peripheral
- Interventions
- Procedure: Korean integrative medicine
- Registration Number
- NCT04905745
- Lead Sponsor
- Jaseng Medical Foundation
- Brief Summary
This is an observational study that evaluate the effectiveness and safety of Korean integrative treatments in patients with peripheral facial nerve palsy. Adulthood patients aged between 19 to 69 who were diagnosed with peripheral facial nerve palsy and receive Korean integrative treatments for facial palsy will be enrolled in the study and the change will be followed according to the Facial disability index (FDI) at the 3 month moment after baseline.
- Detailed Description
This is an observational study that evaluate the effectiveness and safety of Korean integrative treatments in patients with peripheral facial nerve palsy. A total of 100 patients who are in age of from 19 to 69, diagnosed with peripheral facial nerve palsy, in acute to subacute stage, and who receive Korean integrative treatments for facial palsy will be enrolled in this study. This study is an observational study and the intervention will be decided not by researchers, but by physicians in the real clinical practice. The treatment will be entirely determined according to each subject's medical conditions by an experienced clinician who has received more than 6 years of education and more than 3 years of training. This study will only record the contents of the intervention. Among all the data generated during the study period, data deemed necessary can be collected in the case record forms. The intervention will also be determined by the clinician, and the researcher presented assessment and data collection timepoints, which is independent of the treatment schedule. The on-treatment visit schedule will be once a week during the treatment is ongoing, and follow-up visit schedule will be on the 5th, 14th, and 53rd weeks after the baseline.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 100
- age of 19 to 69
- diagnosed with unilateral peripheral facial nerve palsy
- onset of facial palsy within 3 weeks or less.
- an individual who can provide written consent form to participate in the study.
- diagnosed with central nervous system disease causing facial palsy
- secondary facial palsy after multiple sclerosis, tumor, cerebrovascular disease and temporal bone fracture.
- Ramsay-Hunt syndrome
- bilateral or recurrent facial nerve palsy.
- an individual who received any treatment that can have a significant effect on changes in facial paralysis within recent 2 month. (ie. facial nerve decompression surgery)
- already or planned to be pregnant or breast-feeding within the study period.
- uncontrolled diabetes mellitus within the last 3 months.
- within a month after participating any other facial palsy-related clinical trials, or planning to participate other clinical trials within 6 month.
- impossible to read and understand the documents, regarding informed consent form and the questionnaires.
- difficult to participate according to the judgement of researchers.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Facial palsy Korean integrative medicine Adulthood facial palsy patients group who receive Korean integrative medicine.
- Primary Outcome Measures
Name Time Method Facial disability index week 14 This is a questionnaire made to evaluate the subjective sensations of patients on the ability to use facial muscles and their emotional state. It is composed of 10 items, and 1-5 is composed of 5 points per item for movement state, and 6-10 is composed of 6 points per item for sociological state and emotional state.
- Secondary Outcome Measures
Name Time Method Facial nerve grading system (FNGS 2.0) week 1, 5, 14, 53 FNGS 2.0 is calculated based on the total score by section by section in facial part and additional score with synkinesis movement. The result of FNGS 2.0 well indicate the palsy status, with the grade of 1-6 and 4-24 points.
Short Form-12 Health Survey (SF-12) week 1, 5, 14, 53 The SF-12 is a questionnaire that evaluates the overall health-related quality of lives (HRQoL). SF-12 consists of 12 questions covering following 8 areas, to evaluate functional health and well-being of individuals both ill and healthy; physical functioning, role-physical, bodily pain, general health, vitality, social functioning, role-emotional, and mental health.
Patient Global Impression of Change (PGIC) week 5, 14, 53 Patient global impression of change (PGIC) is a method that allows the patient to subjectively evaluate the degree of improvement in 7 degree of scale.
Facial disability index (FDI) week 1, 5, 14, 53 This is a questionnaire made to evaluate the subjective sensations of patients on the ability to use facial muscles and their emotional state. It is composed of 10 items, and 1-5 is composed of 5 points per item for movement state, and 6-10 is composed of 6 points per item for sociological state and emotional state.
Synkinesis Assessment Questionnaire (SAQ) week 1, 5, 14, 53 The SAQ is a questionnaire that calculates the total score of 9 representative symptoms of synkinesis into 1-5 points for each item.
House-Brackmann facial palsy grade system (HB grade) week 1, 5, 14, 53 and every week during treatment (for survival analysis in complete recovery) HB grade is a scale to evaluate facial palsy into 6 stages based on the severity of facial palsy, especially the muscles around the mouth and the muscles arount the eyes.
Numeric rating scale (NRS) week 1, 5, 14, 53 and every week during treatment NRS is a 11-point scale of 0-10. the researcher will rate NRS for postauricular pain and discomforts in the face and cervical area.
Trial Locations
- Locations (1)
Jaseng Hospital of Korean Medicine
🇰🇷Seoul, Gangnam-Gu, Korea, Republic of