Your session is about to expire
← Back to Search
Non-Invasive Spinal Cord Stimulation for Spinal Cord Injury
Study Summary
This trial is testing different ways to help people with spinal cord injuries breathe better. It will compare task-specific training (like respiratory or arm exercises) with non-task-specific stimulation (like electrical stimulation of the spinal cord) to see which is more effective.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
Find a Location
Who is running the clinical trial?
Media Library
- My lung function tests show healthy breathing capacity.You have not received treatment for depression, have a mental health condition, or are currently using drugs excessively.I am 21 years old or older.I have a bone that hasn't healed yet.I have not received treatment for a muscle or joint problem.I have a contracture or pressure sore that hasn't been treated.I am not disabled and meet the study's gender criteria.You have had a spinal cord injury for at least 12 months before joining the study.I have a significant disease affecting my esophagus or digestive system.You have a hormone disorder, cancer, severe obesity, blood clot in a deep vein, or a disease related to HIV/AIDS.I have conditions like anemia or nerve issues causing my dizziness when standing.Your lung function test shows at least a 15% decrease in breathing capacity.I am 18 years old or older.My health condition is stable.I have a history of lung or breathing problems.My selection for the SCI study does not depend on my gender.My spinal cord injury is above T5 and not getting worse.I rely on a machine to help me breathe.I have a serious lung or heart condition.I have a history of heart disease.
- Group 1: Non-Disabled (ND) and Spinal Cord Injured (SCI) controls
- Group 2: Spinal Cord Injured (SCI) intervention groups
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
What are the primary objectives of this medical experiment?
"This medical trial, which is slated to run for approximately one year, seeks to assess non-invasive respiratory electromyography. Secondary objectives include beat-by-beat arterial blood pressure monitoring, functional neurophysiological assessment of motor capacity and control in the upper and lower extremities/trunk, as well as evaluation of handicap using the Craig Handicap Assessment & Reporting Technique (CHART) questionnaire."
Is it possible for me to register in this clinical experiment?
"The investigators of this medical study are looking for 36 volunteers between 18 and 99 years old who have experienced a spinal cord injury. To qualify, applicants must be above the legal age at enrollment, with their condition having remained stable since sustaining their SCI no less than 12 months ago. Additionally, they must demonstrate an FVC or FEV1 deficit of 15% or higher as observed during screening spirometry."
Are there any opportunities to join this research experiment at present?
"Clinicaltrials.gov data suggests that this trial, which was initially posted on May 24th 2023, is not actively recruiting at present. However, 352 other studies are currently searching for volunteers."
Is the upper-age limit for this clinical trial restricted to individuals aged 85 and below?
"This clinical trial is only available to those between 18 and 99 years of age. There are 37 additional studies for minors, as well as 306 trials designed specifically for seniors."
Share this study with friends
Copy Link
Messenger