RECRUITING

Implementation of IVS3 for Upper Limb Motor Recovery

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Conditions

Neglect, HemispatialStroke, CardiovascularMirror MovementMotor Activity

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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

This study measures participant satisfaction and upper extremity function in outpatients with chronic stroke when exposed to the IVS3 device. Investigators hypothesize that treatment with the IVS3 device will be feasible and tolerable for use in the outpatient setting.

Official Title

A Pilot Study on Tolerance and Ease of Implementation of Intensive Visual Stimulation (IVS3) in Daily Practice for Upper Limb Motor Recovery in Outpatient Rehab Center

Quick Facts

Study Start:2024-10-02
Study Completion:2027-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06483230

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 CriteriaExclusion Criteria
  1. 1. Age ≥ 18 years old
  2. 2. English speaking
  3. 3. History of ischemic or hemorrhagic stroke ≥ 6 months prior to study enrolment
  4. 4. FMA-UE: 20 \< x \< 50 (moderate impairments)
  5. 5. With or without hemi spatial neglect
  1. 1. Spasticity or increased tone with MAS ≥3 in the upper extremity
  2. 2. Unable to communicate effectively or provide informed consent
  3. 3. Significant visual impairments
  4. 4. Concurrent occupational therapy being received outside of the study
  5. 5. Pregnant or incarcerated individuals

Contacts and Locations

Study Contact

Mahika Rathod
CONTACT
(212) 746-1509
mar4053@med.cornell.edu

Principal Investigator

Joan Stilling, MD,MS
PRINCIPAL_INVESTIGATOR
Weill Medical College of Cornell University

Study Locations (Sites)

Weill Cornell Medicine, 525 E. 68th St, Baker Pavilion, F-2106
New York, New York, 10065
United States

Collaborators and Investigators

Sponsor: Weill Medical College of Cornell University

  • Joan Stilling, MD,MS, PRINCIPAL_INVESTIGATOR, Weill Medical College of Cornell University

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 Date2024-10-02
Study Completion Date2027-06

Study Record Updates

Study Start Date2024-10-02
Study Completion Date2027-06

Terms related to this study

Additional Relevant MeSH Terms

  • Neglect, Hemispatial
  • Stroke, Cardiovascular
  • Mirror Movement
  • Motor Activity