RECRUITING

Post-Stroke Sensory Reweighting on Walking and Balance Outcomes

Conditions

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The primary objective of this proof-of-concept study is to longitudinally track the development of post-stroke sensory reweighting (PSR), identify associated structural neuroanatomical correlates, and investigate their relationship to walking and fall outcomes.

Official Title

Tracking the Development and Influence of Post-Stroke Sensory Reweighting on Walking and Balance Outcomes

Quick Facts

Study Start:2024-11-01

Study Completion:2026-08-30

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT06727097

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
1. First ever clinical stroke 2. Stroke due to ischemia 3. Age 18 years or older 4. Ability to consent by patient (not surrogate), any time prior to acute hospital discharge	1. Pre-stroke dependence (modified Rankin Scale score of 3 or more) 2. Isolated brainstem or cerebellar stroke 3. Bilateral acute strokes 4. Co-enrollment in a trial of an intervention through six-month follow-up 5. Inability to maintain follow-up with study procedures through six-month follow-up 6. Contraindication to non-contrast MRI 7. Low likelihood of survival beyond the acute hospitalization, such as malignant cerebral edema 8. Pre-existing co-morbid conditions that significantly affects vision, somatosensory function, vestibular system, orthostasis, coordination or mobility 9. Post stroke mRS\>4 or discharge to hospice

Inclusion Criteria

Exclusion Criteria

1. First ever clinical stroke
2. Stroke due to ischemia
3. Age 18 years or older
4. Ability to consent by patient (not surrogate), any time prior to acute hospital discharge

1. Pre-stroke dependence (modified Rankin Scale score of 3 or more)
2. Isolated brainstem or cerebellar stroke
3. Bilateral acute strokes
4. Co-enrollment in a trial of an intervention through six-month follow-up
5. Inability to maintain follow-up with study procedures through six-month follow-up
6. Contraindication to non-contrast MRI
7. Low likelihood of survival beyond the acute hospitalization, such as malignant cerebral edema
8. Pre-existing co-morbid conditions that significantly affects vision, somatosensory function, vestibular system, orthostasis, coordination or mobility
9. Post stroke mRS\>4 or discharge to hospice

Contacts and Locations

Study Contact

oluwole Awosika, MD, MSCR

CONTACT

+1 513 558 2919

awosikoe@ucmail.uc.edu

Colin Drury, MS

CONTACT

513 558 7656

drurycd@ucmail.uc.edu

Principal Investigator

Oluwole Awosika, MD, MSCR

PRINCIPAL_INVESTIGATOR

University of

Study Locations (Sites)

University of Cincinnati College of Medicine

Cincinnati, Ohio, 45267

United States

Collaborators and Investigators

Sponsor: University of Cincinnati

Oluwole Awosika, MD, MSCR, PRINCIPAL_INVESTIGATOR, University of

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-11-01

Study Completion Date2026-08-30

Study Record Updates

Study Start Date2024-11-01

Study Completion Date2026-08-30

Terms related to this study

Additional Relevant MeSH Terms

Ischemic Stroke