ACTIVE_NOT_RECRUITING

intenSive UpPer Extremity Recovery Program for Chronic Stroke (SUPER)

Conditions

Chronic Stroke Rehabilitation Arm recovery High intensity therapy Occupational therapy Physical therapy

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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 purpose of this study is to Investigate the feasibility of a high-quality, high-dose, high-intensity upper extremity therapy program and to assess the treatment effects of a high-quality, high-dose, high-intensity upper extremity therapy program on functional outcomes, motor impairment, and quality of life

Official Title

intenSive UpPer Extremity Recovery Program for Chronic Stroke (SUPER)

Quick Facts

Study Start:2023-03-20

Study Completion:2026-12-31

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05689502

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 to 80 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* Single qualifying stroke event as confirmed by CT or MRI * At least 6 months post stroke * Fugl-Meyer upper extremity (UE) score of 20-45 * Able to follow written instructions * Able to tolerate 6 hours of therapy a day	* Prior arm injury impacting available passive or active range of motion or significant arm pain with movement * Active drug or alcohol abuse * Diagnosed with advanced dementia * Pre-stroke baseline mRS\>3 * History of clinically significant ischemic or hemorrhagic stroke resulting in prior arm weakness in the same territory as the index stroke * Medical instability assessed by the treating stroke physician to participate to the study.

Inclusion Criteria

Exclusion Criteria

* Single qualifying stroke event as confirmed by CT or MRI
* At least 6 months post stroke
* Fugl-Meyer upper extremity (UE) score of 20-45
* Able to follow written instructions
* Able to tolerate 6 hours of therapy a day

* Prior arm injury impacting available passive or active range of motion or significant arm pain with movement
* Active drug or alcohol abuse
* Diagnosed with advanced dementia
* Pre-stroke baseline mRS\>3
* History of clinically significant ischemic or hemorrhagic stroke resulting in prior arm weakness in the same territory as the index stroke
* Medical instability assessed by the treating stroke physician to participate to the study.

Contacts and Locations

Principal Investigator

Sean Savitz

PRINCIPAL_INVESTIGATOR

The University of Texas Health Science Center, Houston

Study Locations (Sites)

The University of Texas Health Science Center at Houston

Houston, Texas, 77030

United States

Collaborators and Investigators

Sponsor: The University of Texas Health Science Center, Houston

Sean Savitz, PRINCIPAL_INVESTIGATOR, The University of Texas Health Science Center, Houston

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 Date2023-03-20

Study Completion Date2026-12-31

Study Record Updates

Study Start Date2023-03-20

Study Completion Date2026-12-31

Terms related to this study

Keywords Provided by Researchers

Rehabilitation
Arm recovery
High intensity therapy
Occupational therapy
Physical therapy

Additional Relevant MeSH Terms

Chronic Stroke