Clinical trial Recruiting at 1 site Observational Ages 40 to 85

Characterising neuromuscular function after stroke

Official title: Characterising the Neuromuscular Function of Stroke Patients During Recovery

Run by University of Nottingham · NCT07013188 · Data updated 2026-11-12

This project will test how stroke affects muscle and nerve control in adults aged 40–85 who had a stroke in the last five years and still have one-sided limb weakness.

Quick facts

Study typeObservational
Ages40 Years to 85 Years
SexAll
Enrollment16 (estimated)
SponsorUniversity of Nottingham
Academic / other
Locations1 site (Derby, Derbyshire)
StatusRecruiting
StartedJune 1, 2024
Main results expectedOctober 1, 2025
Study endsMay 1, 2026
Registry record updatedJune 10, 2025
Trial IDNCT07013188 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 40–85 with a confirmed stroke in the last five years who can give informed consent and report ongoing one-sided limb weakness are ideal candidates.

Probably not a fit

People with dementia or significant cognitive impairment, recent malignancy, serious uncontrolled cardiac or respiratory disease, dialysis dependence, recent steroid/hormone therapy, significant musculoskeletal disorders, or who are wheelchair-dependent are excluded and unlikely to benefit from participation.

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

What this trial studies

This is a pilot observational project recruiting adults aged 40–85 with a confirmed stroke within the past five years who report persistent unilateral limb impairment. Participants will attend the Royal Derby Hospital/University of Nottingham site for detailed neuromuscular assessments, including clinical exams and measurements of muscle activation and function. No experimental therapies are given; collected data will be used to map common patterns of motor deficit. The findings are intended to inform the design of targeted rehabilitation approaches such as constraint-induced movement therapy, functional electrical stimulation, or virtual-reality rehabilitation.

Why it matters

Potential benefit: If successful, the findings could help clinicians tailor rehabilitation therapies to improve arm and leg function after stroke.

How similar studies have gone: Related work shows that targeted rehab methods (CIMT, FES, VR) can improve function, but detailed neuromuscular characterisation specifically in this post-stroke group is still limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* • Aged between 40-85 years

  * Willing and able to give informed consent for participation in the study
  * Had a confirmed stroke within the last 5 years
  * Self-reports persisting post-stroke loss of unilateral limb function

Exclusion Criteria:

* • Diagnosis of cognitive impairment/dementia

  * Current or recent (\<2y) malignancy
  * Severe respiratory disease (e.g., uncontrolled asthma, COPD, pulmonary hypertension)
  * Active cardiovascular disease: Uncontrolled hypertension (BP\>160/100mmHg); Recent (\<12mo) cardiac event; Heart failure (Class III/IV); Significant arrhythmia; Unstable angina
  * Metabolic disease: Untreated hyper/hypoparathyroidism; Cushing's disease
  * Significant musculoskeletal disorders (based on clinical opinion)
  * Dialysis patients
  * Recent steroid treatment within 6 months or hormone replacement therapy
  * Mobility dependant (wheelchair dependency)

Where it's running

  • Royal Derby Hospital branch, School of Medicine, University of Nottingham
    Derby, Derbyshire, United Kingdom
    Recruiting

Similar studies

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

  • Stroke care during COVID-19 waves: patterns in admissions and treatments

    This study tests how stroke and TIA care patterns changed during the later waves of the COVID-19 pandemic by analyzing hospital data on admissions, stays, thrombolysis, and thrombectomy.

    Recruiting at 4 sites Johannes Gutenberg University Mainz · Prague and 3 other locations · NCT07795021

  • Health for Hungary: Long-term blood and health data collection to study aging and disease onset

    This study tests whether routine blood tests plus advanced molecular analyses can help detect the early stages of non-communicable diseases in adults over 40.

    Recruiting at 21 sites Center for Molecular Fingerprinting Research Nonprofit LLC · Balatonfüred and 32 other locations · NCT07743021

  • Self-Supervised Constraint-Induced Movement Therapy for Stroke Recovery

    This study tests a partly self-guided therapy program to help adults recover the use of their weaker arm after stroke, aiming to require less time with a therapist.

    Recruiting Ohio State University · Columbus, Ohio · NCT07723300

  • Pemafibrate for Symptomatic ICAS

    This study tests whether pemafibrate can help prevent worsening of intracranial artery narrowing in people with symptomatic ICAS and high triglycerides after a stroke or TIA.

    Recruiting at 37 sites Tokyo Women's Medical University · Toyoake, Aichi-ken and 41 other locations · NCT07562178

  • Using IMPROVE to guide carotid revascularisation decisions

    This trial tests whether using the IMPROVE MRI-based score to select patients for carotid revascularisation is as good as standard care based mainly on stenosis degree, among people who have had a recent stroke or TIA due to carotid disease.

    Recruiting Maastricht University Medical Center · Arnhem, Gelderland and 9 other locations · NCT07556887

  • NORAHOME: Home-based multimodal monitoring and care for people with minor stroke and TIA

    This project tests whether giving adults with minor stroke or TIA a multimodal home-hospitalization program can be as safe, reduce complications, and be more efficient than standard hospital care.

    Recruiting Hospital Universitari Vall d'Hebron Research Institute · Barcelona · NCT07500116

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.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.