- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT03577444
Role of Genetic Polymorphism in Neuroplasticity Involved in Dysphagia Recovery
Przegląd badań
Szczegółowy opis
Neurogenic dysphagia attributable to acquired brain lesions, such as after stroke and after traumatic brain injury, are one of leading causes of chronic disability world widely and it is expected to substantially increase over the next two decades. Among various sequalae, dysphagia can be observed in about 40% -60% of post-stroke patients and 20% -30% of them might suffer from recurrent aspiration pneumonia and may inhibit recovery and can even lead to death. Recovery after brain lesions can be explained by specific molecular events. It is proven that Genetic polymorphisms associated with impaired neural repair or plasticity might reduce recovery from stroke. Not only for the motor recovery, but genetic polymorphism is also crucial for the recovery of swallowing after stroke, however, only limited amount of studies are available. Therefore, it is urgent to determine whether the recovery of swallowing disorders after stroke is affected by the inherent polymorphism of the patient, whether the degree of recovery and brain plasticity associated with swallowing depend on the gene characteristics and polymorphism of the patient and whether recovery in swallowing parallel to the recovery observed in other functional areas (ie. hand recovery, truncal control recovery, ADL recovery).
Based on the results of this study, results will be expected to help provide genetically tailored diagnosis and prognostication according to the gene polymorphism of the patient. Optimized treatment of the patient is expected to contribute to prevention of respiratory complications and improve functional outcome related to swallowing after stroke.
Typ studiów
Zapisy (Rzeczywisty)
Kontakty i lokalizacje
Lokalizacje studiów
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Gyonggido
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Bucheon, Gyonggido, Republika Korei, 14647
- Department of Rehabilitation Medicine
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Kyounggido
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Bucheon, Kyounggido, Republika Korei
- Department of Rehabilitation Medicine Bucheon St Mary's Hospital, Catholic University of Korea, College of Medicine
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dziecko
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Metoda próbkowania
Badana populacja
Opis
Inclusion Criteria
- Patients who had been diagnosed with first ever brain lesions ( stroke and traumatic brain lessons) and referred to Department of Rehabilitation( in Bucheon St. Mary's Hospital and National Traffic Injury Rehabilitation Hospital)
- Patients who were hospitalized for 30 days and were followed up at 3 months after the onset of brain lesions
- Patients who agree to participate in the study or if the guardian or legal representative agrees only if the patient has difficulties in consenting or consenting to participate directly in the language disability.
- In the case of a suspected feeding swallowing disorder in the patient, the patient should be confirmed by VFSS(Videofluoroscopic Swallwing Study) or FEES(Fiberoptic Endoscopic Evaluation of Swallowing)
Exclusion Criteria
- Patients who do not meet the above criteria
- Patients with difficulty in collecting blood for genetic testing
- Patients who were not able to followed-up for 6 months(follow up loss patients)
- Patients with long-term Parkinson's disease, Alzheimer's disease, Guillain-Barre syndrome, myasthenia gravis syndrome, etc.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
Kohorty i interwencje
Grupa / Kohorta |
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Dysphagia patients
Patients who had been diagnosed with neurogenic dysphagia related to either stroke or traumatic brain injury at two university affiliated hospitals
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
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Change in Functional Oral Intake Scale(FOIS)
Ramy czasowe: initial 4 weeks,3months after onset
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Functional oral intake scale(FOIS) is categorical scale range from 1 indicating severe dysphagia and 7 indicating safe oral feeding.
Higher change in FOIS indicates improvement of patient's swallowing function.
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initial 4 weeks,3months after onset
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
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Change in Berg Balance Scale(BBS)
Ramy czasowe: initial 4 weeks, 3 months after onset
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BBS is a scale that measure person's static and dynamic balance abilities, ranging from 0 to 56 where 56 indicated independence in gait and 0 means unable to gait.
Higher change in Berg Balance Scale means improved patient's mobility.
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initial 4 weeks, 3 months after onset
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Change in Medical Research Council(MRC) grade Disability level
Ramy czasowe: initial 4 weeks, 3 months after onset
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The modified Rankin Scale (mRS) is a commonly used scale for measuring the degree of disability or dependence in the daily activities of people who have suffered a stroke or other causes of neurological disability. It is categorical value with the the scale running from 0-6, running from perfect health without symptoms to death. |
initial 4 weeks, 3 months after onset
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Change in K-MBI(Korean Modified Barthel Index)
Ramy czasowe: initial 4 weeks, 3 months after onset
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The Barthel scale or Barthel ADL index is an ordinal scale used to measure performance in activities of daily living (ADL).
Each performance item is rated on this scale with a given number of points assigned to each level or ranking.
Higher scores indicates indolence in ADL activities.
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initial 4 weeks, 3 months after onset
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Change in FAC(Functional Ambulatory Category)
Ramy czasowe: initial 4 weeks, 3 months after onset
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The Functional Ambulation Categories (FAC) is a functional walking test that evaluates ambulation ability.
This 6-point scale assesses ambulation status by determining how much human support the patient requires when walking, regardless of whether or not they use a personal assistive device .
Higher scores indicate better performance.
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initial 4 weeks, 3 months after onset
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Change in Fugyl Meyer score from baseline
Ramy czasowe: initial 4 weeks, 3 months after onset
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The Fugl-Meyer Assessment for upper extremity (FMA-UE)is considered to assess the body function according to the International Classification of Functioning, Disability and Health (ICF) with a maximum score of 66 points)
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initial 4 weeks, 3 months after onset
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Change in MMSE-K(Korean Minimental Status Examination)
Ramy czasowe: initial 4 weeks,3months after onset
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3. The Mini-Mental State Examination (MMSE) is a 30-point questionnaire that is used extensively to measure cognitive impairment.[1]
Higher score indicates better cognitive function.
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initial 4 weeks,3months after onset
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Change in scores of Quality of Life Survey score (EQ5D(EuroQol-5 dimension)
Ramy czasowe: initial 4 weeks, 3months after onset
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The QOLS is a reliable and valid instrument for measuring quality of life from the perspective of the patient The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression.
Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems.
The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions.
This decision results in a 1-digit number that expresses the level selected for that dimension.
The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state.
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initial 4 weeks, 3months after onset
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Change in Penetration-Aspiration Scale(PAS)
Ramy czasowe: 4 weeks, 3 months after onset
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initial PAS is a categorical scale that measures level of penetration of bolus(food) into airway at pharynx.
It ranges from Score 1 to 8, where 1 indicated no airway entrance of bolus and 8 indicated glottic passage of food.
Higher change in PAS indicates improvement in patient's swallowing function.
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4 weeks, 3 months after onset
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Change in dysphagia outcome rating scale
Ramy czasowe: 4 weeks, 3 months after onset
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initial The Dysphagia Outcome and Severity Scale (DOSS) is a simple, easy-to-use, 7-point scale developed to systematically rate the functional severity of dysphagia based on objective assessment and make recommendations for diet level, independence level, and type of nutrition with level 1 indicating severe dysphagia and level 7 indicating normal swallowing function.
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4 weeks, 3 months after onset
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Change in SWAL-QOL(swallowing quality of life)) survey score
Ramy czasowe: 4 weeks, 3 months after onset
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initial SWAL-QOL is a survey that evaluation patient's subjective quality of life within their swallowing function.
Scored will be sumed up where higher score indicates better quality of life.
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4 weeks, 3 months after onset
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Number of events associated with aspiration pneumonia
Ramy czasowe: 4 weeks, 3 months after onset
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initial Diagnosis of aspiration pneumonia will be based on ≥3 of the following features: fever (>38°C), productive cough, abnormal respiratory examination, abnormal chest radiograph; specifically involving the dependent portions of the lung; white blood cell count >12,000/mL, or isolation of a relevant pathogen and use of antibiotics)
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4 weeks, 3 months after onset
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Współpracownicy i badacze
Sponsor
Śledczy
- Dyrektor Studium: TaeWoo Kim, National Traffic Rehabilitation Hospital Korea
Publikacje i pomocne linki
Publikacje ogólne
- Park HY, Kim Y, Oh HM, Kim TW, Park GY, Im S. Potential Prognostic Impact of Dopamine Receptor D1 (rs4532) Polymorphism in Post-stroke Outcome in the Elderly. Front Neurol. 2021 Jun 30;12:675060. doi: 10.3389/fneur.2021.675060. eCollection 2021.
- Oh HM, Kim TW, Park HY, Kim Y, Park GY, Im S. Role of rs6265 BDNF polymorphisms and post-stroke dysphagia recovery-A prospective cohort study. Neurogastroenterol Motil. 2021 Jan;33(1):e13953. doi: 10.1111/nmo.13953. Epub 2020 Aug 9.
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- NTRH-18001
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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Badania kliniczne na Uderzenie
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