What this study is
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.
What's being tested
- No intervention
Intervention · OTHER
This is an observational study
Study details
- Sponsor
- University of Minnesota
- Conditions
- Spinal Cord Injuries
- Enrolling
- 80 people
- Starts
- 2024-11-18
- Est. completion
- 2027-06-15
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years and overSex ALLHealthy volunteers AcceptedYou may qualify if
- 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.
You can't join if
- 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.
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openUniversity of Minnesota
Minneapolis, Minnesota, United States
- Sydney Carpentier · Contact562-508-9693carpe749@umn.edu
Recruiting
Study team
Sponsor
University of Minnesota
Study ID PMR-2023-32512
Principal investigator
Ann Van de Winckel
University of Minnesota
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.