Registry for Patients with Stroke
STroke RehabilitATion rEgistrY for Predicting Functional Outcomes
Fondazione Don Carlo Gnocchi Onlus · NCT05389878
This study is creating a registry to collect information from stroke patients to better understand their rehabilitation needs and improve their care.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 600 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Fondazione Don Carlo Gnocchi Onlus (other) |
| Locations | 4 sites (Florence and 3 other locations) |
| Trial ID | NCT05389878 on ClinicalTrials.gov |
What this trial studies
This study aims to implement a registry that collects demographic, clinical, and functional data from stroke patients to enhance understanding and treatment of stroke rehabilitation. It follows a minimal assessment protocol established by the Italian Society of Physical and Rehabilitation Medicine to evaluate rehabilitation needs and outcomes. The registry will gather data at patient admission and discharge, along with follow-up assessments at three and six months post-stroke. The goal is to develop data-driven prognosis prediction models to improve patient care.
Who should consider this trial
Good fit: Ideal candidates include adults over 18 years old who have experienced an ischemic or hemorrhagic stroke within the last six months.
Not a fit: Patients with severe acquired brain injuries or life-threatening conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this registry could lead to improved rehabilitation strategies and outcomes for stroke patients.
How similar studies have performed: Other studies utilizing registries for stroke patients have shown promise in improving outcomes and understanding of stroke rehabilitation.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult patients (over 18 years of age) with ischemic or haemorrhagic stroke, first event or with relapse, time to onset of stroke less than 6 months, signature of informed consent by the patient or family member. Exclusion Criteria: * Patients from Severe Acquired Brain Injuries units and / or with diseases that threaten the patient's life
Where this trial is running
Florence and 3 other locations
- IRCCS Fondazione Don Carlo Gnocchi — Florence, Italy (RECRUITING)
- IRCCS Fondazione Don Carlo Gnocchi Santa Maria Rinascente — Milan, Italy (NOT_YET_RECRUITING)
- Fondazione Don Gnocchi, Centro Santa Maria ai Servi — Parma, Italy (NOT_YET_RECRUITING)
- Fondazione Don Carlo Gnocchi Centro "Spalenza" — Rovato, Italy (NOT_YET_RECRUITING)
Study contacts
- Principal investigator: Francesca Cecchi, MD — IRCCS Fondazione don Carlo Gnocchi
- Study coordinator: Francesca Cecchi, MD
- Email: fcecchi@dongnocchi.it
- Phone: +393388627184
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Stroke, Registry, Outcome, Predictors