RECRUITING

Upper Extremity Training for Chronic Cervical Spinal Cord Injury

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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 is to understand how the combination of activity-based recovery training and targeted spinal cord transcutaneous stimulation (scTS) can improve participants' ability to use their hand, arms, and core.

Official Title

Neuromodulation Training for Upper Extremity Recovery for Chronic Cervical Spinal Cord Injury

Quick Facts

Study Start:2021-06-14

Study Completion:2027-11-15

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT04921592

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
* 18 years of age. * spinal cord injury for greater than or equal to 6 months. * spinal cord injury at a cervical neurologic level of injury.	* ventilator dependent. * history of fractures. * pressure sore or skin issues. * history of illicit drug abuse. * history of cardiac, respiratory, bladder, renal or other medical disorder unrelated to spinal cord injury. * bladder Botox injections less than 12 months prior. * muscle Botox injections less than 12 months prior. * colostomy bag or urostomy. * implanted pump (i.e., baclofen pump, pain pump, etc). * If I am female: I am pregnant at the time of enrollment or planning to become pregnant during the course of the study. * unable to wean from anti-spasticity medication. * contraindications to MRI imaging (pacemaker, metallic foreign body, aneurysm clip, etc.)

Inclusion Criteria

Exclusion Criteria

* 18 years of age.
* spinal cord injury for greater than or equal to 6 months.
* spinal cord injury at a cervical neurologic level of injury.

* ventilator dependent.
* history of fractures.
* pressure sore or skin issues.
* history of illicit drug abuse.
* history of cardiac, respiratory, bladder, renal or other medical disorder unrelated to spinal cord injury.
* bladder Botox injections less than 12 months prior.
* muscle Botox injections less than 12 months prior.
* colostomy bag or urostomy.
* implanted pump (i.e., baclofen pump, pain pump, etc).
* If I am female: I am pregnant at the time of enrollment or planning to become pregnant during the course of the study.
* unable to wean from anti-spasticity medication.
* contraindications to MRI imaging (pacemaker, metallic foreign body, aneurysm clip, etc.)

Contacts and Locations

Study Contact

LeighAnn Martinez, BA

CONTACT

973.324.3557

lmartinez@kesslerfoundation.org

Principal Investigator

Gail F Forrest, PhD

PRINCIPAL_INVESTIGATOR

Kessler Foundation

Study Locations (Sites)

Kessler Foundation

West Orange, New Jersey, 07052

United States

Collaborators and Investigators

Sponsor: Kessler Foundation

Gail F Forrest, PhD, PRINCIPAL_INVESTIGATOR, Kessler Foundation

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 Date2021-06-14

Study Completion Date2027-11-15

Study Record Updates

Study Start Date2021-06-14

Study Completion Date2027-11-15

Terms related to this study

Additional Relevant MeSH Terms

Spinal Cord Injuries