Data from: Preliminary efficacy of cognitive multisensory rehabilitation for neuropathic pain in chronic spinal cord injury: A phase I randomized controlled trial
Data files
Apr 21, 2026 version files 50.66 KB
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DATA_AIRP_for_Dryad_5.2.2023_no_identifiers.csv
8.99 KB
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DATA_AIRP_for_Dryad_5.2.2023_no_identifiers.xlsx
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DATA_AIRP_for_Dryad_Legend_book.csv
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README.md
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Abstract
Neuropathic pain affects 69 % of adults with spinal cord injury (SCI) and responds poorly to current treatments. Emerging evidence suggests that impaired mental body representations (MBR) may contribute to neuropathic pain. We aimed to identify changes in neuropathic pain, and sensorimotor function after Cognitive Multisensory Rehabilitation (CMR), a physical therapy which improves MBR, vs usual care. In this Phase I randomized delayed-treatment trial, 26 adults with SCI-related neuropathic pain were randomized to either 6 weeks of immediate CMR (group A), with 6-week+1-year follow-up; or a 6-week observational period+6-week CMR+1-year follow-up (Group B). We assessed neuropathic pain intensity, sensorimotor function, and SCI-related outcome measures.
https://doi.org/10.5061/dryad.7h44j1007
Description of the data and file structure
This readme.txt file was generated on <20241121> by
Recommended citation for the data: will be completed upon publication of the article
GENERAL INFORMATION
This pilot clinical trial looked at the effects of a physical therapy approach, called cognitive multisensory rehabilitation for adults with spinal cord injury-related neuropathic pain. The data collected are patient-reported outcome measures (e.g., pain measures, sleep questionnaires, etc) taken at 2 or 3 timepoints (pre-and post intervention, and at 1-year follow-up).
1. Title of Dataset: Data used for Preliminary Efficacy of Cognitive Multisensory Rehabilitation for Neuropathic Pain in Chronic Spinal Cord Injury: A Phase I Randomized Controlled Trial.
2. Author Information
Principal Investigator Contact Information
Name: Ann Van de Winckel
Institution: Division of Physical Therapy and Rehabilitation Science, Department of Family Medicine and Community Health, Medical School, University of Minnesota
Address: 420 Delaware ST SE, Minneapolis, MN 55455
Email: avandewi@umnn.edu
ORCID: 0000-0001-8400-3177
3. Date published or finalized for release: The manuscript is published in Scientific Reports.
4. Date of data collection (single date, range, approximate date)
5. Geographic location of data collection (where was data collected?): Minnesota
6. Information about funding sources that supported the collection of the data:
- The AIRP2-IND-30: Academic Investment Research Program (AIRP) University of Minnesota School of Medicine funded this study (IRB no. STUDY00008476; ClinicalTrials.gov Identifier: NCT04706208)
- Additional support is provided by the National Center for Advancing Translational Sciences of the National Institutes of Health Award Number UL1TR002494 and UM1TR004405
- the Biotechnology Research Center: P41EB015894
- the National Institute of Neurological Disorders & Stroke Institutional Center Core Grants to Support Neuroscience Research: P30 NS076408
- the High-Performance Connectome Upgrade for Human 3T MRI scanner: 1S10OD017974.
- Image processing resources were provided by the Minnesota Supercomputing Institute (MSI) at the University of Minnesota.
Clinical Trial registration: ClinicalTrials.gov, NCT04706208; first registration 08/01/2021; first participant enrolled 09/01/2021.
Funding: AIRP2-IND-30 (University of Minnesota School of Medicine); UL1TR002494; P41EB015894; P30 NS076408; 1S10OD017974.
7. Overview of the data (abstract): This xls file contains brief clinical/behavioral data of adults with spinal cord injury-related neuropathic pain.
Files and variables
File: DATA_AIRP_for_Dryad_5.2.2023_no_identifiers.xlsx
Description:
- 1. Number of variables: 30
- 2. Number of cases/rows: 26
- 3. Missing data codes: colored spaces (gray with a dot)
- 4. Variable List: See legend book in the xlsx file
- All variables are scores of assessments. There is no coding used to categorize variables.
Variables
- Numeric pain rating scale
Interpretation for this study: highest, average defined as most of the time, and lowest neuropathic pain in the prior week (3 variables) - Numeric pain rating scale for average nociceptive pain in the prior week (1 variable)
- International SCI Pain Basic Data Set Version 2.0: interference of neuropathic pain with activity, mood, and sleep (3 variables)
- ISNCSCI ASIA test: Touch sensation, pin prick sensation, lower limb strength (Average of left and right leg) (3 variables)
- Secondary outcomes questionnaire for adults with SCI (1 variable)
- Spasm frequency and intensity (2 variables)
- Patient-specific functional scale (average of 3 self-identified functional activities) (1 variable)
- SCI-FI/AT for paraplegia: basic mobility, self-care, fine motor function, ambulation (4 variables)
- Pittsburgh Sleep Quality Index
- Trait anxiety inventory (1 variable)
- State anxiety inventory (1 variable)
- Patient health questionnaire - 9: symptoms of depression (1 variable)
- Revised Body Awareness Rating Questionnaire (1 variable)
- Tampa scale of kinesiophobia (1 variable)
- World health organization quality of life - dimension 1 to 4 (4 variables)
- Moorong Self Efficacy Scale (1 variable)
- Physical Activity Enjoyment Scale (1 variable)
DATA_AIRP_for_Dryad_Legend_book.csv and DATA_AIRP_for_Dryad_5.2.2023_no_identifiers.csv are formatting-free versions of the same data in CSV format.
Code/software
DATA & FILE OVERVIEW
1. File List
A. Filename: DATA_AIRP_for_Dryad_5.2.2023_no_identifiers.xlsx
Short description: xls file contains brief clinical/behavioral data of adults with spinal cord injury-related neuropathic pain
METHODOLOGICAL INFORMATION
1. Description of methods used for collection/generation of data: REDCap (community-dwelling adults with SCI)
2. Methods for processing the data: xls and regular statistical software packages
3. Instrument- or software-specific information needed to interpret the data: Regular statistical software packages
4. Standards and calibration information, if appropriate: NA
5. Environmental/experimental conditions: NA
6. Describe any quality-assurance procedures performed on the data: REDCap has a system in place that all cells need to be completed.
7. People involved with sample collection, processing, analysis and/or submission: Ann Van de Winckel (principal investigator)
Access information
Other publicly accessible locations of the data:
- Only on Data Repository for the U of Minnesota (DRYAD)
Data was derived from the following sources:
- Xls file contains brief clinical/behavioral data of adults with spinal cord injury-related neuropathic pain derived from data collection on REDCap
Questionnaires were completed on the UMN REDCap platform. Data were exported to xls.
Excel
