Modeling outcomes in patients with acquired brain injuries

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study focuses on patients with acquired brain injuries (ABI) to predict recovery trajectories using artificial intelligence algorithms. By analyzing various demographic, clinical, and psychosocial factors, the study aims to improve the understanding of recovery patterns and enhance rehabilitation strategies. Data will be collected from patients diagnosed with severe ABI within three months of the injury, allowing for a comprehensive assessment of recovery potential. The goal is to provide clinicians with better predictive tools for patient outcomes.

Why it matters

Who can join: the full rules

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

Where it's running

• Institute for Biomedical Research and Innovation (IRIB) - National Research Council (CNR)
  Messina, Italy Recruiting

Study contacts

• Principal investigator: Antonio Cerasa — Institute for Biomedical Research and Innovation (IRIB) - National Research Council (CNR)
• Study coordinator: Antonio Cerasa
• Email: antonio.cerasa@irib.cnr.it
• Phone: +393339633511

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Co-designed wrist-hand orthosis for children with neuromotor disorders

  In children aged 6 to 14 with neuromotor conditions after brain injury, researchers are testing a wrist-hand brace designed with input from the kids to see if it fits better and is easier to use than their current orthosis.

  Recruiting IRCCS Eugenio Medea · Bosisio Parini · NCT07861958

• Portable MRI for kids with hypoxic brain injury

  This study tests whether a bedside, low-field portable MRI can accurately detect hypoxic-ischemic brain injuries in children compared with standard imaging.

  Recruiting Children's Mercy Hospital Kansas City · Kansas City, Missouri · NCT07577336

• Monitoring beta-lactam antibiotics and kidney clearance in ICU patients with acute brain injury

  This project tries to see if checking kidney clearance together with blood drug levels can quickly identify ICU patients with acute brain injury who need higher doses of beta-lactam antibiotics.

  Recruiting Centre Hospitalier Universitaire de Nīmes · Nîmes · NCT06999161

• Biofeedback training for vision loss after brain injury

  This study is testing if biofeedback training can help people with vision loss from brain injuries see better and improve their quality of life.

  Recruiting University Health Network, Toronto · Toronto, Ontario · NCT06995313

• Evaluation of patients with traumatic and hypoxic-ischemic brain injuries

  This study is trying to understand how brain injuries from trauma or lack of oxygen affect kids and young adults under 20, to find better ways to help them.

  Recruiting Fondazione Policlinico Universitario Agostino Gemelli IRCCS · Rome, Lazio · NCT06873477

• Prebiotic treatment to improve gut health and brain function after injury

  This study is testing if a type of dietary fiber called Inulin can improve gut health and help reduce fatigue and cognitive problems in people recovering from brain injuries.

  Recruiting The University of Texas Medical Branch, Galveston · Galveston, Texas · NCT06607523

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.