Registry for Patients with Stroke
Official title: STroke RehabilitATion rEgistrY for Predicting Functional Outcomes
Run by Fondazione Don Carlo Gnocchi ETS · NCT05389878 · Data updated 2026-11-12
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 |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 600 (estimated) |
| Sponsor | Fondazione Don Carlo Gnocchi ETS Academic / other |
| Locations | 4 sites (Florence and 3 other locations) |
| Status | Recruiting |
| Started | January 12, 2022 |
| Main results expected | June 30, 2026 |
| Study ends | June 30, 2026 |
| Registry record updated | March 11, 2025 |
| Trial ID | NCT05389878 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults over 18 years old who have experienced an ischemic or hemorrhagic stroke within the last six months.
✕Probably not a fit
Patients with severe acquired brain injuries or life-threatening conditions may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
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.
Why it matters
Potential benefit: If successful, this registry could lead to improved rehabilitation strategies and outcomes for stroke patients.
How similar studies have gone: Other studies utilizing registries for stroke patients have shown promise in improving outcomes and understanding of stroke rehabilitation.
Who can join: the full rules
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 it's running
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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
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Deep phenotyping to explore recovery in young adults after stroke
This project will test whether a detailed health and sample-collection approach (deep phenotyping) is practical and acceptable for people aged 18–55 who have had a stroke.
-
Stem cell therapy for chronic stroke recovery
This study is testing whether using a patient's own stem cells can help people with long-term stroke recovery feel better and improve their daily functioning.
-
AI-based tools to help diagnose, treat and predict stroke outcomes across multiple hospitals
This study tests AI-powered tools on real-world stroke patients to see if they can improve pre-hospital triage, diagnosis, and outcome prediction while data stay securely within each hospital.
-
Web-based therapy using action observation and mirror therapy for arm weakness after stroke
This trial tests whether a mobile telerehabilitation app delivering action observation therapy (AOT) alone or combined AOT with mirror therapy (AOT-MT) can improve upper limb function in people with subacute stroke.
-
Remote Ischaemic Conditioning for Fatigue After Stroke 2
Aat least 12 weeks after stroke, adults with post-stroke fatigue will try a simple hand-arm cuff treatment at home to see if it helps reduce fatigue.
-
Dual-task balance training plus computer-based cognitive training after stroke
In adults who recently had a stroke, the study tests whether adding computerized cognitive exercises to balance training improves balance and other recovery outcomes.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.