NCT07411573Active, not recruiting
Multimodal Neurofunctional Profiling in Stroke
A Prospective Observational Cohort Study of Multimodal Neurofunctional Profiling in Patients With Stroke
Source: ClinicalTrials.gov · Last updated 17 Feb 2026
Brief summary (registry, in English)
This prospective, observational cohort study aims to characterize multimodal neurofunctional profiles in patients with stroke. By integrating neurophysiological signals, neuroimaging data, clinical assessments, and biological samples, the study seeks to delineate patterns of brain function and their associations with clinical outcomes. The findings are intended to support improved risk stratification, phenotypic classification, and a deeper understanding of the neurobiological mechanisms underlying stroke-related functional impairment and recovery.
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 1000 (estimated)
- First submitted
- 9 Feb 2026
- Start date
- 20 Jan 2026
- Primary completion date
- 1 Dec 2028
- Lead sponsor
- Peking Union Medical College Hospital
- Diseases
- Stroke
- NCT number
- NCT07411573
What you commit to
- Study type: Observational
- Planned participants: 1000
- From 20 Jan 2026 to the primary completion date, 1 Dec 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Pre-existing neurological conditions resulting in severe baseline motor disability that would confound FMA-based outcome assessment (e.g., prior stroke with significant residual deficits, advanced neurodegenerative disorders).
Other illness
- Contraindications to required non-invasive assessments (e.g., scalp conditions or implanted electronic devices incompatible with EEG/fNIRS, where applicable).
Other
- Inability to comply with study procedures or follow-up schedule, as determined by the investigators.
- Participation in another interventional clinical trial that, in the opinion of the investigators, could interfere with the outcomes of this observational study.
Who the study is looking for
- Adults aged ≥18 years at the time of enrollment.
- Clinical and/or neuroimaging-confirmed diagnosis of stroke (ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage, as applicable).
- Ability to undergo non-invasive neurofunctional assessments (e.g., EEG and/or fNIRS).
- Ability to complete standardized neurological and functional assessments, including the Fugl-Meyer Assessment (FMA), or availability of a legally authorized representative to provide consent and facilitate participation.
- Provision of written informed consent by the participant or legally authorized representative.
Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences Coordinator of this site? Confirm its status | Beijing | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.