Monitoring upper limb movement in stroke patients
Monitoring Post Stroke Upper-Limb Movement in The Wild
This study is trying to see how tracking daily arm movements in stroke patients can help us understand their recovery and improve rehabilitation methods.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 40 (estimated) |
| Ages | 18 Years to 85 Years |
| Sex | All |
| Sponsor | Adi Negev-Nahalat Eran Academic / other |
| Locations | 1 site (Ofakim) |
| Trial ID | NCT06497881 on ClinicalTrials.gov |
What this trial studies
This observational study aims to monitor daily upper limb movements in individuals who have experienced a stroke, linking these movements to recovery and impairment measures. The research is part of The Natural History of Stroke Recovery project, where investigators will develop and validate an algorithm and software using Inertial Measuring Units (IMUs) to track upper limb activity. Additionally, the study will assess proprioception acuity through muscle synergy analysis using surface electromyography (EMG). The relationship between daily movements and recovery levels will be explored to enhance understanding of stroke rehabilitation.
Who should consider this trial
Good fit: Ideal candidates include individuals over 18 years old who were independent in daily activities prior to their stroke and are currently receiving rehabilitation.
Not a fit: Patients with degenerative neurological conditions, significant psychiatric issues, or severe orthopedic conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved rehabilitation strategies for stroke patients by providing insights into movement quality and recovery.
How similar studies have performed: While this approach is innovative, similar studies utilizing movement monitoring in stroke rehabilitation have shown promise in enhancing recovery outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * \>18 years of age * Independent in all activities of daily living before the stroke. * In- and out-patients at Adi-Negev Nahalat-Eran rehabilitation center. * Medically stable * Able to provide informed consent. Exclusion Criteria: * The presence of any degenerative neurological condition, neuropathy, myopathy or Polio that are not secondary to stroke, excluding diabetic related changes. * Traumatic brain injury and/or extra-cerebral hemorrhage. * Significant psychiatric condition, including alcoholism and drug abuse. * Any severe orthopedic condition (such as amputation or severe pain that limits activity) or chronic pain syndrome.
Where this trial is running
Ofakim
- Adi-Negev Nahalat Eran — Ofakim, Israel (Recruiting)
Study contacts
- Principal investigator: Lior Smuelof, PhD — Ben-Gurion University of the Negev
- Study coordinator: Lior Smuelof, PhD
- Email: shmuelof@gmail.com
- Phone: 972547510795
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.