Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT07029802

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

Led by University of Minnesota · Updated on 2025-06-19

80

Participants Needed

1

Research Sites

134 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is twofold: (1) Develop a new evaluation scale for mental body representations (MBR, i.e., body awareness and visuospatial body maps) for adults with spinal cord injury (SCI) with and without neuropathic pain. (2) Assess the psychometric properties of usability, reliability, and validity of the new evaluation scale This is a cross-sectional observational study design. For Aim 1, this study will involve initial item generation for a novel MBR evaluation scale for SCI through email communication, and individual interviews proctored remotely through Zoom, or, if preferred by the participant, in-person. For Aim 2, the study will include a Zoom call for consenting and questionnaires, as well as an in-person visit where participants will be tested with the new SCI-BodyMap evaluation scale, and a questionnaire asking about the usability and satisfaction of the new evaluation scale.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults 18 years or older
  • Control group: uninjured adults from contact lists or recruitment flyers
  • SCI group: adults 18 years or older with complete or incomplete spinal cord injury for at least 1 year
  • Medically stable participants
  • Able to read and understand English
  • Access to the internet and a device (iPad, computer, phone) and willing to attend in-person testing at the University of Minnesota
Not Eligible

You will not qualify if you...

  • Uncontrolled seizure disorder
  • Cognitive impairment or communication disability preventing understanding or learning
  • Dependence on a ventilator
  • Major medical complications
  • Pressure ulcers that prevent prolonged sitting or lying down

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Minnesota

Minneapolis, Minnesota, United States, 55455

Actively Recruiting

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Research Team

S

Sydney Carpentier

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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