Completed

Wheelchair Backs That Support the Spinal Curves: Assessing Postural and Functional Changes

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What is being tested

Manual Wheelchair (MWC) backrest configuration

Other
Who is being recruted

Central Nervous System Diseases+3

+ Nervous System Diseases

+ Spinal Cord Diseases

From 18 to 70 Years
+13 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Supportive Care Study

Interventional
Study Start: December 2021
See protocol details

Summary

Principal SponsorCraig Hospital
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: December 1, 2021

Actual date on which the first participant was enrolled.

A properly fit wheelchair and seating system can have a profound impact on the daily life of people with spinal cord injury (SCI). A backrest that supports the natural spinal curves is thought to enhance posture, functional mobility, and comfort for manual wheelchair (MWC) users. In fact, therapists routinely prescribe after-market posture-backs based on clinical reasoning. However, there is little research comparing the efficacy of an after-market posture-back to the standard upholstery back, and it is becoming increasingly difficult to justify these to group insurance payers. Based on this, investigators performed a pilot study to investigate whether there were postural and/or functional differences between using a standard upholstery WC back and an after-market solid posture-back. The results of that study have been presented at the American Congress of Rehabilitation Medicine (ACRM) annual conference in November 2019 and the Combined Sections Meeting (CSM) of the American Physical Therapy Association (APTA) in February 2020, and were also published in the Journal of Spinal Cord Medicine in 2020. Although the results of that study demonstrated clinical relevance and statistical trends for improvements in postural alignment and functional outcomes when using a solid back, there was not enough power to establish statistical significance. It also did not evaluate the effect of backrest height and position or depth of contour in order to inform clinical practice. The overall objective of this fully powered clinical trial is to further investigate if using a solid backrest on MWC will improve postural alignment, function and wheelchair mobility, as compared with an upholstery backrest; and to explore the impact of overall back height, seat gap, and contour when using a solid backrest.

Official TitleWheelchair Backs That Support the Spinal Curves: Assessing Postural and Functional Changes
NCT05068648
Principal SponsorCraig Hospital
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

100 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Supportive Care Study

These studies explore ways to improve comfort and daily life for people living with a condition. They may focus on easing symptoms, reducing treatment side effects, or supporting overall well-being.


Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 70 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Central Nervous System DiseasesNervous System DiseasesSpinal Cord DiseasesSpinal Cord InjuriesWounds and InjuriesTrauma, Nervous System

Criteria

4 inclusion criteria required to participate
Full time manual wheelchair users

Motor complete SCI from C6-T4

Age 18-70 at time of testing

Time since injury > 3 month at time of testing

9 exclusion criteria prevent from participating
Weight >250 pounds

Current pressure ulcer at time of testing

Significant shoulder pain that precludes independent mobility at time of testing

Insufficient range of motion to achieve neutral pelvis and spine at time of testing

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

5 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Active Comparator
standard upholstery back that promotes posterior pelvic tilt set at or below cushion level and 1" above inferior angle

Group II

Active Comparator
active contour back positioned with seat gap and with free scapulae

Group III

Active Comparator
active contour back positioned with seat gap and with blocked scapulae

Group IV

Active Comparator
deep contour back positioned with seat gap and with free scapulae

Group 5

Active Comparator
deep contour back positioned without seat gap and with free scapulae

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 3 locations

Suspended

Craig Hospital

Englewood, United StatesOpen Craig Hospital in Google Maps
Suspended

Shirley Ryan AbilityLab

Chicago, United States
Suspended

Kessler Institute for Rehabilitation

West Orange, United States
Completed3 Study Centers