Recruiting

Observational Study

Sponsor:

Baylor University

Code:

NCT07280923

Conditions

Neurologic Disorders

Spinal Cord Injury

Stroke

Traumatic Brain Injury

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Interview

Study Details

Brief summary:

This study is testing the psychometric properties of a new tool to determine recommendations for pressure relief frequency in wheelchair users.

Conditions

Neurologic Disorders

Spinal Cord Injury

Stroke

Traumatic Brain Injury

Study ID

NCT07280923

Start date

Dec, 2025

Status verified date

Dec, 2025

Completion date

Jan, 2027

Anticipated

Primary completion date

Dec, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • primary wheelchair user
  • diagnosed with a neurologic disorder

Exclusion Criteria:

  • does not use a wheelchair for more than 50% of waking hours

Study Design

Enrollment

15 participants

Anticipated

Interventions and Outcome Measures

Arms

Wheelchair Users

Individuals with a neurologic disorder who are primary wheelchair users

Interventions

Interview

Participants will be interviewed for this study. No intervention will occur.

Primary outcome measure

  • Interview [ Time Frame: Baseline ]

Central Contacts and Locations

Central contacts

Locations

Baylor University

Recruiting

Waco, Texas, United States, 76798

Contacts

More Information

Sponsor

Baylor University

Last update posted

Dec 23, 2025

Last verified

Dec, 2025

Keywords

  • wheelchair user
  • pressure relief
  • skin integrity

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Baylor University on 2025-12-23.