- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT07711119
Cross-cultural Adaptation and Multicenter Validation of the Italian Versions of the Brief Evaluation of Receptive Aphasia (BERA) and SWallowing Assessment in Disorders of Consciousness (SWADOC)
14 lipca 2026 zaktualizowane przez: Alfonso Magliacano
Adattamento Trans-culturale e Validazione Multicentrica Della Versione Italiana Delle Scale Brief Evaluation of Receptive Aphasia (BERA) e SWallowing Assessment in Disorders of Consciousness (SWADOC)
Patients with severe acquired brain injury may evolve from coma into prolonged disorders of consciousness.
In these patients, residual language comprehension and swallowing abilities are difficult to evaluate because standard assessments often depend on verbal or motor responses.
The Brief Evaluation of Receptive Aphasia (BERA) assesses receptive language abilities through visual/eye-movement responses, whereas the SWallowing Assessment in Disorders of Consciousness (SWADOC) assesses oral and pharyngeal components of swallowing in patients with disorders of consciousness.
This national multicenter observational study aims to perform the Italian cross-cultural adaptation and validation of BERA and SWADOC.
Consecutive adult inpatients with severe acquired brain injury and disorders of consciousness will be recruited from four Italian centers.
SWADOC will be administered to 57 patients, and BERA will be administered to a nested subgroup of 22 patients who meet additional criteria.
Inter-rater reliability, test-retest reliability over 24 hours, and convergent validity with Coma Recovery Scale-Revised scores will be analyzed.
Przegląd badań
Status
Jeszcze nie rekrutacja
Szczegółowy opis
This study is part of the Horizon MSCA DoC-Box project, which aims to develop a multimodal toolbox to support fast and reliable diagnosis of disorders of consciousness.
The study includes two consecutive phases.
In Phase 1, the original French versions of BERA and SWADOC will be translated into Italian by two expert translators.
The translated versions will be synthesized, back-translated into the original language by two independent blinded translators, compared, discussed, and revised by researchers and experts according to international guidelines for translation and cultural adaptation.
In Phase 2, the Italian versions will be evaluated in a multicenter observational validation study involving three Fondazione Don Carlo Gnocchi centers (Sant'Angelo dei Lombardi, Florence, Milan) and the IRCCS Istituto Neurologico Carlo Besta in Milan.
After diagnostic confirmation based on repeated CRS-R assessments, Examiner A will administer the SECONDs to assess the level of consciousness.
On the same day, Examiner B will administer the Italian BERA and/or SWADOC, while Examiner C will independently score the scales to assess inter-rater agreement.
After approximately 24 hours, Examiner A will repeat the SECONDs, and either Examiner B or Examiner C will repeat BERA and/or SWADOC to assess test-retest reliability.
Demographic and clinical variables, level of consciousness, total scores, and subscale scores will be entered in a centralized pseudonymized REDCap database and analyzed in aggregate form.
Typ studiów
Obserwacyjny
Zapisy (Szacowany)
79
Kontakty i lokalizacje
Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.
Kontakt w sprawie studiów
- Nazwa: Anna Estraneo, MD
- E-mail: aestraneo@dongnocchi.it
Kopia zapasowa kontaktu do badania
- Nazwa: Alfonso Magliacano, PhD
- Numer telefonu: 393387389414
- E-mail: amagliacano@dongnocchi.it
Lokalizacje studiów
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Florence, Włochy
- IRCCS Fondazione Don Carlo Gnocchi
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Kontakt:
- Bahia Hakiki
- Numer telefonu: 3905573931
- E-mail: bhakiki@dongnocchi.it
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Milan, Włochy
- IRCCS Istituto Neurologico Carlo Besta
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Kontakt:
- Matilde Leonardi
- Numer telefonu: 390223941
- E-mail: Matilde.Leonardi@istituto-besta.it
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Milan, Włochy
- IRCCS SM Nascente Fondazione Don Carlo Gnocchi
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Kontakt:
- Angela Comanducci
- Numer telefonu: 3902403081
- E-mail: acomanducci@dongnocchi.it
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AV
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Sant'Angelo dei Lombardi, AV, Włochy, 83054
- Polo Specialistico Riabilitativo Fondazione Don Gnocchi
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Kontakt:
- Alfonso Magliacano
- Numer telefonu: 393387389414
- E-mail: amagliacano@dongnocchi.it
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Kryteria uczestnictwa
Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
Nie
Metoda próbkowania
Próbka bez prawdopodobieństwa
Badana populacja
Adult inpatients with severe acquired brain injury and a stable diagnosis of disorder of consciousness consecutively admitted to the four participating Italian rehabilitation/neurorehabilitation centers and meeting the inclusion/exclusion criteria.
Opis
Inclusion Criteria:
- Age >= 18 years.
- Native Italian speaker.
- Diagnosis of severe acquired brain injury.
- At least 28 days since the acute event.
- For SWADOC validation: stable clinical diagnosis of disorder of consciousness, including UWS, MCS, or EMCS, assessed with the Coma Recovery Scale-Revised repeated at least five times over two weeks.
- For BERA validation: stable clinical diagnosis of MCS or EMCS assessed with the Coma Recovery Scale-Revised repeated at least five times over two weeks.
- For BERA validation: presence of visual fixation and/or visual pursuit assessed with the Coma Recovery Scale-Revised.
- No remote history of neurological, neurodegenerative, or psychiatric disease; for SWADOC validation, no remote history of otorhinolaryngological disease.
- Written informed consent provided by the primary caregiver/legal representative according to local regulations.
Exclusion Criteria:
- Occurrence of a second cerebral event between enrollment and data collection.
- Unstable general clinical condition preventing assessment, including but not limited to need for ventilatory support, severe infection, or status epilepticus.
Plan studiów
Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.
Jak projektuje się badanie?
Szczegóły projektu
Kohorty i interwencje
Grupa / Kohorta |
Interwencja / Leczenie |
|---|---|
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Patients with severe acquired brain injury and disorders of consciousness
Consecutive adult inpatients with severe acquired brain injury and a stable diagnosis of disorder of consciousness admitted to one of the four participating centers and meeting eligibility criteria.
All eligible participants will undergo SWADOC validation assessments.
A nested subgroup of the first 22 participants who also meet BERA-specific criteria will undergo BERA validation assessments.
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Structured clinical assessment of oral and pharyngeal swallowing components in patients with disorders of consciousness.
The Italian version will be administered and scored by trained examiners to evaluate inter-rater and test-retest reliability.
Brief clinical assessment of receptive language abilities, including phonology, semantics, and morphosyntax.
Responses are based on visual/eye-movement behavior, allowing assessment of patients unable to communicate verbally or through reliable motor responses.
It will be administered to the nested subgroup meeting BERA-specific criteria.
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Inter-rater reliability of the Italian Swallowing Assessment in Disorders of Consciousness total score
Ramy czasowe: Day 1, during the first assessment session
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Inter-rater reliability will be assessed for the total score of the Italian version of the Swallowing Assessment in Disorders of Consciousness.
The SWADOC total score ranges from 0 to 24, with higher scores indicating better preserved swallowing abilities.
The reported outcome will be the intraclass correlation coefficient for agreement between independent raters.
The intraclass correlation coefficient is a unitless reliability coefficient ranging from 0 to 1, with higher values indicating greater inter-rater reliability.
The SWADOC quantitative scoring system includes 8 scored items rated from 0 to 3, allowing calculation of oral and pharyngeal subscores and a total score.
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Day 1, during the first assessment session
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Test-retest reliability of the Italian Swallowing Assessment in Disorders of Consciousness total score
Ramy czasowe: Baseline and approximately 24 hours later
|
Test-retest reliability will be assessed for the total score of the Italian version of the Swallowing Assessment in Disorders of Consciousness.
The SWADOC total score ranges from 0 to 24, with higher scores indicating better preserved swallowing abilities.
The reported outcome will be the intraclass correlation coefficient between the baseline assessment and the reassessment performed approximately 24 hours later.
The intraclass correlation coefficient is a unitless reliability coefficient ranging from 0 to 1, with higher values indicating greater test-retest reliability.
|
Baseline and approximately 24 hours later
|
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Inter-rater reliability of the Italian Brief Evaluation of Receptive Aphasia total score
Ramy czasowe: Day 1, during the first assessment session
|
Inter-rater reliability will be assessed for the total score of the Italian version of the Brief Evaluation of Receptive Aphasia in the eligible subgroup of patients.
The BERA total score ranges from 0 to 30, with higher scores indicating better receptive language abilities.
The reported outcome will be the intraclass correlation coefficient for agreement between independent raters.
The intraclass correlation coefficient is a unitless reliability coefficient ranging from 0 to 1, with higher values indicating greater inter-rater reliability.
The BERA includes 30 items per version, with 10 phonological, 10 semantic, and 10 morphosyntactic items; each correct visual fixation response is scored as 1 point and errors or absent fixation as 0 points.
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Day 1, during the first assessment session
|
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Test-retest reliability of the Italian Brief Evaluation of Receptive Aphasia total score
Ramy czasowe: Baseline and approximately 24 hours later
|
Test-retest reliability will be assessed for the total score of the Italian version of the Brief Evaluation of Receptive Aphasia in the eligible subgroup of patients.
The BERA total score ranges from 0 to 30, with higher scores indicating better receptive language abilities.
The reported outcome will be the intraclass correlation coefficient between the baseline assessment and the reassessment performed approximately 24 hours later.
The intraclass correlation coefficient is a unitless reliability coefficient ranging from 0 to 1, with higher values indicating greater test-retest reliability.
|
Baseline and approximately 24 hours later
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Convergent validity of the Italian Swallowing Assessment in Disorders of Consciousness total score with the Coma Recovery Scale-Revised total score
Ramy czasowe: Baseline/Day 1
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Convergent validity will be assessed by calculating the Spearman rank correlation coefficient between the total score of the Italian version of the Swallowing Assessment in Disorders of Consciousness and the total score of the Coma Recovery Scale-Revised.
The SWADOC total score ranges from 0 to 24, with higher scores indicating better preserved swallowing abilities.
The Coma Recovery Scale-Revised total score ranges from 0 to 23, with higher scores indicating a higher level of consciousness.
The reported outcome will be Spearman's rho, a unitless correlation coefficient ranging from -1 to +1.
|
Baseline/Day 1
|
|
Convergent validity of the Italian Brief Evaluation of Receptive Aphasia total score with the Coma Recovery Scale-Revised total score
Ramy czasowe: Baseline/Day 1
|
Convergent validity will be assessed by calculating the Spearman rank correlation coefficient between the total score of the Italian version of the Brief Evaluation of Receptive Aphasia and the total score of the Coma Recovery Scale-Revised.
The BERA total score ranges from 0 to 30, with higher scores indicating better receptive language abilities.
The Coma Recovery Scale-Revised total score ranges from 0 to 23, with higher scores indicating a higher level of consciousness.
The reported outcome will be Spearman's rho, a unitless correlation coefficient ranging from -1 to +1.
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Baseline/Day 1
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Współpracownicy i badacze
Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.
Sponsor
Współpracownicy
Śledczy
- Główny śledczy: Alfonso Magliacano, PhD, Fondazione Don Carlo Gnocchi
Daty zapisu na studia
Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.
Główne daty studiów
Rozpoczęcie studiów (Szacowany)
1 września 2026
Zakończenie podstawowe (Szacowany)
31 sierpnia 2028
Ukończenie studiów (Szacowany)
31 sierpnia 2028
Daty rejestracji na studia
Pierwszy przesłany
9 lipca 2026
Pierwszy przesłany, który spełnia kryteria kontroli jakości
14 lipca 2026
Pierwszy wysłany (Rzeczywisty)
17 lipca 2026
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
17 lipca 2026
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
14 lipca 2026
Ostatnia weryfikacja
1 lipca 2026
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
- Objawy neurologiczne
- Choroby mózgu
- Choroby ośrodkowego układu nerwowego
- Choroby Układu Nerwowego
- Zaburzenia psychiczne
- Rany i urazy
- Manifestacje neurobehawioralne
- Zaburzenia neurokognitywne
- Uraz czaszkowo-mózgowy
- Uraz, układ nerwowy
- Zaburzenia komunikacji
- Zaburzenia językowe
- Afazja
- Zaburzenia mowy
- Stany patologiczne, oznaki i objawy
- Objawy i symptomy
- Urazy mózgu
- Zaburzenia świadomości
- Afazja, Wernicke
Inne numery identyfikacyjne badania
- BERA-SWADOC
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
NIEZDECYDOWANY
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Nie
Bada produkt urządzenia regulowany przez amerykańską FDA
Nie
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .