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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03962582
Other study ID # STU00205806
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2017
Est. completion date March 30, 2019

Study information

Verified date May 2019
Source Shirley Ryan AbilityLab
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study tests using a wheelchair back that supports the spine in a neutral position and one that allows the spine and pelvis to fall into a posterior pelvic tilt.


Description:

Individuals will randomly start with the supportive back vs the unsupportive back. Measurements of the spine and pelvis will be taken. Forward upward reach, one stroke push, times forward push and ramp skills will be assessed.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date March 30, 2019
Est. primary completion date March 30, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- complete spinal cord injury with levels

- Full time wheelchair users

- English speaking in order to understand the consent

Exclusion Criteria:

- Over 250 pounds in body weight

- Inability to grip a wheelchair push rim

- Individual with pressure ulcer

- Individual with shoulder pain

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Matrix back
The Matrix back will replace the individual's back and the measures will be taken.

Locations

Country Name City State
United States Shirley Ryan AbilityLab Chicago Illinois

Sponsors (4)

Lead Sponsor Collaborator
Shirley Ryan AbilityLab Craig Hospital, Motion Concepts, The Craig H. Neilsen Foundation

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Seated Body Measurements performed. Angle measurements will be taken when sitting. These include the pelvic angle (femur to pelvis) and Spinal Angle of Kyphosis (femur to acromion). 2 hour session (one visit)
Primary Vertical Forward Reach Test (VFRT): Assesses stability by measuring the maximum distance an individual can reach forward vertically (upward) while sitting in a fixed position. 2 hour session (one visit)
Primary Breathing status: An instrument called a spirometer is placed into the mouth with the nose clipped and the individual is instructed to take a deep breath and blow out. Peak effort flow, peak cough flow, and functional capacity will be recorded. 2 hour session (one visit)
Primary One stroke push: This measures how far the wheelchair moves forward with one stroke over carpet. 2 hour session (one visit)
Primary Timed forward Wheeling/Wheelchair Propulsion Test (WPT): The WPT is a brief test measuring the number of wheelchair pushes and time needed to cross a distance of 23 meters 2 hour session (one visit)
Primary Ramp Ascent (forward wheeling This is a timed test on a 10.3 meter ramp with a 1:13 grade slope 2 hour session (one visit)
Primary Pain Scale: The participant will rate any pain felt while sitting in the test wheelchairs after all activities using a numerical scale of 0-10, with 0 being no pain. 2 hour session (one visit)
Primary Survey The study team developed a survey for patients to fill out asking questions such as comfort of back support and opinions of practicality of back support. 2 hour session (one visit)
Secondary Breathing status: Pulse oximetry will be taken with the person sitting in each testing wheelchair. 2 hour session (one visit)
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