Clinical trial Recruiting at 1 site Observational Ages 18 and up

A new scale to measure body awareness and spatial body maps in adults with spinal cord injury

Official title: Development of a Novel Evaluation Scale of Mental Body Representation (MBR) for Adults With Spinal Cord Injury

Run by University of Minnesota · NCT07029802 · Data updated 2026-11-12

This study will test a new questionnaire to measure body awareness and visuospatial body maps in adults with spinal cord injury, including those with and without neuropathic pain.

More Spinal Cord Injuries trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment80 (estimated)
SponsorUniversity of Minnesota
Academic / other
Locations1 site (Minneapolis, Minnesota)
StatusRecruiting
StartedNovember 18, 2024
Main results expectedJune 15, 2027
Study endsJune 15, 2027
Registry record updatedJune 18, 2026
Trial IDNCT07029802 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are adults aged 18 or older with a complete or incomplete spinal cord injury of at least one year who are medically stable, read English, have internet access and can attend an in-person visit at the University of Minnesota, alongside uninjured adult controls aged 18+ for comparison.

Probably not a fit

People with uncontrolled seizure disorders, significant cognitive or communication impairments from brain injury, ventilator dependence, major medical complications, or pressure ulcers preventing prolonged sitting or lying are unlikely to be eligible or to benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This cross-sectional observational study will develop and validate a novel Mental Body Representation (MBR) scale tailored for adults with spinal cord injury (SCI). Initial item generation will be done through email and individual interviews conducted remotely via Zoom or in person, followed by psychometric testing. Consenting and baseline questionnaires will occur over Zoom, and participants will complete the new SCI-BodyMap during an in-person visit to examine usability, reliability, and validity. The study includes both adults with chronic SCI (≥1 year) and uninjured adult controls for comparison.

Why it matters

Potential benefit: If successful, the SCI-BodyMap could provide clinicians and researchers a reliable, easy-to-use tool to track body awareness and help tailor rehabilitation or pain management.

How similar studies have gone: Psychometric development using remote interviews followed by in-person testing has been successful for related patient-reported outcome measures, but a dedicated MBR scale specifically for SCI is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

Control group

* Uninjured adults (from the contact list with the Brain Body Mind lab or through fliers or StudyFinder)
* 18+ years old adults

SCI group

* 18+ years old, participants with an incomplete or complete SCI of ≥ 1 year
* medically stable
* able to read and understand English
* having access to the internet/iPad/computer/phone and willing to come in for an in-person testing at the University of Minnesota.

Exclusion Criteria:

SCI group

* Uncontrolled seizure disorder;
* cognitive impairment and/or communicative disability (e.g., due to brain injury) preventing them from following directions or from learning;
* ventilator dependency;
* major medical complications;
* pressure ulcers hindering prolonged sitting or lying down.

Where it's running

  • University of Minnesota
    Minneapolis, Minnesota, United States
    Recruiting

Study contacts

  • Principal investigator: Ann Van de Winckel — University of Minnesota
  • Study coordinator: Sydney Carpentier
  • Email: carpe749@umn.edu
  • Phone: 562-508-9693

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.