Understanding recovery after stroke
Learning the Natural History of Recovery After Stroke - Cognitive, Motor and Sensory Function
Adi Negev-Nahalat Eran · NCT06441552
This study is tracking how people recover after a stroke by looking at their thinking, movement, and feeling abilities over time to see how different rehab programs can help them feel better.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 200 (estimated) |
| Ages | 18 Years to 85 Years |
| Sex | All |
| Sponsor | Adi Negev-Nahalat Eran (other) |
| Locations | 3 sites (Haifa and 2 other locations) |
| Trial ID | NCT06441552 on ClinicalTrials.gov |
What this trial studies
This longitudinal observational study aims to track the recovery process following a stroke by monitoring changes in cognitive, motor, and sensory functions over time. It is part of the RESTRO project, which evaluates a neurorehabilitation program designed to enhance recovery and quality of life for stroke patients. Data will be collected from three primary sites over a period of 6 to 12 months, allowing researchers to analyze the relationship between rehabilitation intensity and patient outcomes.
Who should consider this trial
Good fit: Ideal candidates include adults over 18 who were independent in daily activities before their first or recurrent stroke and are currently medically stable.
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 provide valuable insights into effective rehabilitation strategies that enhance recovery after stroke.
How similar studies have performed: Other studies focusing on stroke recovery and rehabilitation have shown promising results, indicating that this approach is grounded in existing research.
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, with first ever stroke, or with a recurrent stroke that did not lead to disability (were independent in ADL before the second stroke). * 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. * Participation in another interventional study.
Where this trial is running
Haifa and 2 other locations
- Rambam/Technion — Haifa, Israel (NOT_YET_RECRUITING)
- Adi-Negev Nahalat Eran — Ofakim, Israel (RECRUITING)
- Al-Ahli hospital — Hebron, Palestinian Territories (NOT_YET_RECRUITING)
Study contacts
- Principal investigator: Simona Bar-Haim, PhD — Ben-Gurion University of the Negev
- Study coordinator: Simona Bar-Haim, PhD
- Email: barhaims@bgu.ac.il
- Phone: 972-54-470-2553
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.
Conditions: Cerebral Vascular Accident/Stroke