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Modeling Outcome in Patients With Acquired Brain Injuries

Modeling Trajectories of Functional Outcome in Patients With Severe Acquired Brain Injuries Using a Non-Linear Dynamic Evolution Approach.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06162091
Acronym
MOF-ABI
Enrollment
190
Registered
2023-12-08
Start date
2024-01-10
Completion date
2025-05-31
Last updated
2025-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain Injuries

Keywords

acquired brain injury, functional outcome, Modeling trajectories, mathematical models

Brief summary

Acquired brain injury (ABI) is the leading cause of death and disability worldwide. The degree of severity varies according to a combination of numerous demographics, etiological, clinical, cognitive, behavioral, psychosocial and environmental factors, which can interfere with the effectiveness of rehabilitation interventions and, therefore, with the final outcome. The most important goal of the modern clinic is to predict in time the progression of possible recovery after the brain injury event in order to provide more effective treatment, but the high heterogeneity and clinical variability and the unpredictability of the onset of comorbidities makes this a hard target to reach. In recent years, artificial intelligence algorithms have been applied to more precisely define the role of critical variables that can help clinical practice to predict the final outcome. The classical approach of these algorithms provides only probabilistic values on the final outcome, without considering the typology of clinical interventions and overall complications that may appear throughout the hospitalization period. The objective of this multicentric study is to define a new statistical approach that can describe the dynamics of individual clinical changes occuring during the inpatient intensive rehabilitation care period. The proposed approach combines a principal component analysis (PCA) for dimension reduction (capturing the maximum amount of information and reducing the dimensionality problem) and a nonlinear mathematical modeling for describing the evolution of the clinical course in terms of the resulting new PCA dimensions. By using this approach, we may determine the individual patient's temporal trajectories while examining particular clinical factors. The secondary objective of this study is to validate a new version of the Early Rehabilitation Barthel Index (ERBI), a well-known clinical scale used to measure functional changes in patients with severe acquired brain injury.

Interventions

OTHERData collection

The study will involve at the time of entry into the rehabilitation setting, the collection of data related to demographic and clinical variables assessing: 1. The Level of responsiveness (Coma Recovery Scale -revised (CRS-r); 2. Cognitive functioning (Levels of Cognitive Functioning, LCF); 3. disability (Disability Rating Scale, DRS); 4. level of care needed (Early Rehabilition Barthel Index, ERBI) The Final outcome measure will be the Glasgow Outcome Scale- Extended (GOSE). It will also collect data on clinical variables and presence of medical devices (e.g. decompressive craniectomy, hydrocephalus, tracheostomy, respiration). For all evaluations, two monthly timepoints will be conducted for a total of 12 timepoints until discharge (0 -6 months). If the patient will be hospitalized for more than 6 months, the assessment will be done monthly up to 12 months.

Sponsors

Istituto S.Anna Crotone
CollaboratorUNKNOWN
IRCCS Centro Neurolesi Bonino Pulejo
CollaboratorOTHER
Centro Cardinal Ferrari, Fontanellato, Parma
CollaboratorUNKNOWN
Fondazione Istituto G. Giglio, Cefalù (PA)
CollaboratorUNKNOWN
Habilita Istituto di Neuroriabilitazione, Zingonia (BG)
CollaboratorUNKNOWN
Casa Sollievo della Sofferenza IRCCS
CollaboratorOTHER
IRCCS Istituto delle Scienze Neurologiche di Bologna
CollaboratorOTHER
IRCCS Sacro Cuore Don Calabria di Negrar
CollaboratorOTHER
Fondazione Salvatore Maugeri
CollaboratorOTHER
Istituti Clinici Zucchi
CollaboratorOTHER
Istituto Clinico Humanitas
CollaboratorOTHER
Istituto Medicina Fisica E Riabilitazione Gervasutta, Udine
CollaboratorUNKNOWN
Montecatone Rehabilitation Institute S.p.A.
CollaboratorOTHER
Ospedale Di Riabilitazione Fondazione Santa Lucia, Roma
CollaboratorUNKNOWN
Ospedale San Giovanni Battista, Foligno (PG)
CollaboratorUNKNOWN
Ospedale Ss. Trinità Di Fossano, Cuneo
CollaboratorUNKNOWN
Fondazione Don Carlo Gnocchi Onlus
CollaboratorOTHER
Istituto per la Ricerca e l'Innovazione Biomedica
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients with clinical diagnosis of severe acquired brain injury of different etiology (traumatic, hemorrhagic vascular,ischemic vascular, anoxic, infectious, other etiology * interval since the acute occurrence that led to the clinical condition of ≤3 months duration * age of 18 years or older * informed consent signed by family member/caregiver/supporting caregiver

Exclusion criteria

* Positive remote medical history of pre-existing disabling neurological or orthopedic conditions and psychiatric disorders

Design outcomes

Primary

MeasureTime frameDescription
Glasgow Outcome Scale - ExtendedThe test needs approximately 5 minutes to complete.The Glasgow Outcome Scale - Extended (GOS-E) is a widely used outcome instrument to assess disability and recovery after brain injury. There are 8 categories in the scale: 1 - Dead, 2 - Vegetative State, 3 - Low Severe Disability, 4- Upper Severe Disability, 5- Low Moderate Disability, 6- Upper Moderate Disability, 7- Low Good Recovery and 8-Upper Good Recovery. The minimum score is 1 (dead) and the maximum score is 8 (upper good recovery).

Secondary

MeasureTime frameDescription
Early Rehabilition Barthel IndexThe test needs approximately 20 minutes to complete.The Early Rehabilition Barthel Index (ERBI) is usually used to measure functional changes in patients with severe acquired brain injury. ERBI consists of 17 items grouped into two sections, A and B. Section A consists of six negative items that can be given the scores - 50 and 0, and one item with scores -25 and 0. Section B corresponds to the original Barthel Index, with ten positive items, with three scores: 0, 5 and 10. The total from section A ranges from - 325 to 0 points, the total from section B from 0 to l00. Therefore, the final total, given by A + B, ranges from -325 (the worst) to +l 00 (the best).

Countries

Italy

Contacts

Primary ContactAntonio Cerasa
antonio.cerasa@irib.cnr.it+393339633511
Backup ContactMaria Valeria Maiorana
mariavaleria.maiorana@irib.cnr.it

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026