Actively Recruiting

Age: 18Years - 85Years
All Genders
Healthy Volunteers
NCT06441552

The Natural History of Recovery After Stroke

Led by Adi Negev-Nahalat Eran · Updated on 2025-10-03

200

Participants Needed

3

Research Sites

152 weeks

Total Duration

On this page

Sponsors

A

Adi Negev-Nahalat Eran

Lead Sponsor

B

Ben-Gurion University of the Negev

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this longitudinal observational study is to learn the course of recovery after stroke. Specifically, in this study we will learn and describe the changes in cognitive, motor and sensory function over time in stroke patients.

CONDITIONS

Official Title

The Natural History of Recovery After Stroke

Who Can Participate

Age: 18Years - 85Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Over 18 years of age
  • Independent in all activities of daily living before the stroke
  • Receiving care as an in-patient or out-patient at Adi-Negev Nahalat-Eran rehabilitation center
  • Experiencing first-ever stroke or recurrent stroke without disability (independent in daily activities before second stroke)
  • Medically stable
  • Able to provide informed consent
Not Eligible

You will not qualify if you...

  • Having degenerative neurological conditions, neuropathy, myopathy, or Polio not caused by stroke (except diabetic-related changes)
  • History of traumatic brain injury or extra-cerebral hemorrhage
  • Significant psychiatric conditions, including alcoholism or drug abuse
  • Severe orthopedic conditions limiting activity or chronic pain syndrome
  • Participation in another interventional study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Rambam/Technion

Haifa, Israel

Not Yet Recruiting

2

Adi-Negev Nahalat Eran

Ofakim, Israel

Actively Recruiting

3

Al-Ahli hospital

Hebron, Palestinian Territories

Not Yet Recruiting

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Research Team

S

Simona Bar-Haim, PhD

CONTACT

L

Lior Smuelof, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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