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Recruiting NCT06441552

NCT06441552 The Natural History of Recovery After Stroke

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Clinical Trial Summary
NCT ID NCT06441552
Status Recruiting
Phase
Sponsor Adi Negev-Nahalat Eran
Condition Cerebral Vascular Accident (CVA)/Stroke
Study Type OBSERVATIONAL
Enrollment 200 participants
Start Date 2024-02-01
Primary Completion 2027-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 85 Years
Study Type OBSERVATIONAL
Interventions
non-interventional

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 200 participants in total. It began in 2024-02-01 with a primary completion date of 2027-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility 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.

Contact & Investigator

Central Contact

Simona Bar-Haim, PhD

✉ barhaims@bgu.ac.il

📞 972-54-470-2553

Principal Investigator

Simona Bar-Haim, PhD

PRINCIPAL INVESTIGATOR

Ben-Gurion University of the Negev

Frequently Asked Questions

Who can join the NCT06441552 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 85 Years, studying Cerebral Vascular Accident (CVA)/Stroke. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06441552 currently recruiting?

Yes, NCT06441552 is actively recruiting participants. Contact the research team at barhaims@bgu.ac.il for enrollment information.

Where is the NCT06441552 trial being conducted?

This trial is being conducted at Haifa, Israel, Ofakim, Israel, Hebron, Palestinian Territories.

Who is sponsoring the NCT06441552 clinical trial?

NCT06441552 is sponsored by Adi Negev-Nahalat Eran. The principal investigator is Simona Bar-Haim, PhD at Ben-Gurion University of the Negev. The trial plans to enroll 200 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology