Using MEG to Evaluate Recovery After Minor Stroke
Official title: Imaging the Network: Using MEG to Determine the Pathophysiology Underlying Post-Stroke Cognitive Impairment
Run by Johns Hopkins University · NCT04188522 · Data updated 2026-11-12
This study is testing how well people recover their thinking skills after a minor stroke by using special brain scans at 1 and 6 months after the stroke.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 100 Years |
| Sex | All |
| Enrollment | 55 (estimated) |
| Sponsor | Johns Hopkins University Academic / other |
| Locations | 1 site (Baltimore, Maryland) |
| Status | Recruiting |
| Started | July 1, 2018 |
| Main results expected | June 30, 2027 |
| Study ends | June 30, 2027 |
| Registry record updated | June 5, 2026 |
| Trial ID | NCT04188522 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 18 and older who have experienced a minor ischemic stroke and exhibit cognitive deficits.
✕Probably not a fit
Patients with primary intracerebral hemorrhage or significant prior neurological diseases 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 observational study investigates cognitive recovery in patients who have experienced a minor stroke using magnetoencephalography (MEG). Participants will undergo MEG testing at 1 and 6 months post-stroke to assess brain activity during cognitive tasks related to executive function, attention, and multi-tasking. The study aims to better understand the cognitive difficulties faced by stroke survivors, which may not correlate with the size or location of brain lesions. The research will involve collaboration with the University of Maryland to enhance data collection and analysis.
Why it matters
Potential benefit: If successful, this study could lead to improved understanding and management of cognitive recovery in stroke patients.
How similar studies have gone: While the use of MEG in stroke recovery is a novel approach, similar studies have shown promise in understanding cognitive deficits post-stroke.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Adults (≥18 years) admitted to Bayview Medical Center Neurology. 2. Evidence of acute ischemic stroke (CT or MRI)- lacunar stroke or branch occlusion (M3/A3/P3 or smaller) OR NIHSS ≤ 8 on admission. 3. Competent speaker of English (by self or family report) prior to stroke. 4. Return for follow-up 4-6 weeks post event (+/- 4 wks). 5. Cognitive deficits present on initial testing.\*\* unique to MEG study 6. Willing to travel to the University of Maryland twice for MEG.\*\* unique to MEG study 7. Fully independent functionally and able to travel to the University of Maryland unassisted.\*\* unique to MEG study Exclusion Criteria: 1. Primary intracerebral hemorrhage- as evidenced by blood on head CT or MRI. 2. Previous neurological disease (e.g., dementia, multiple sclerosis, prior symptomatic stroke). Incidental asymptomatic lacunar strokes found on imaging will not be excluded as prior disease. 3. Uncorrected hearing or visual loss. 4. Large vessel occlusion. 5. Presence of any of the following that would lead to significant artifact on MEG: cardiac pacemaker, intracranial clips, metal implants, or external clips within 10mm of the head, metal in the eyes.\*\* unique to MEG study 6. Claustrophobia, obesity, and/or any other reason leading to difficulty staying in the MEG for up to 1 hour.\*\* unique to MEG study 7. For controls- clinical history of stroke or other neurological dysfunction (seizure, multiple sclerosis, etc.); psychiatric disease
Where it's running
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Johns Hopkins Bayview Medical Center
Baltimore, Maryland, United States Recruiting
Study contacts
- Principal investigator: Elisabeth B Marsh, MD — Johns Hopkins School of Medicine
- Study coordinator: Elisabeth B Marsh, MD
- Email: ebmarsh@jhmi.edu
- Phone: 410-550-8703
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Accelerated repetitive transcranial magnetic stimulation (rTMS) versus sham for post-stroke apathy
This project will try a faster course of rTMS to see if it reduces persistent apathy in people at least six months after an ischemic or hemorrhagic stroke.
-
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.
-
Wrist-worn device to encourage use of the weaker arm after a recent stroke
This trial tests whether a wrist-worn sensor system plus motor and behavioral home coaching helps people 1–6 months after a stroke with moderate arm weakness use their affected arm more than a usual home-exercise program.
-
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.
-
Trans-spinal magnetic stimulation for improving mobility in chronic stroke patients
This study is testing if a new type of magnetic treatment can help improve walking and movement in adults who have had a stroke for a long time.
-
Telehealth program for lifestyle changes in stroke survivors
This study tests whether a telehealth program can help stroke survivors make healthy lifestyle changes with support from others over six months.
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.