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NCT04951297 Clinical Trial

Development and Validation of a Bowel-routine-based Self Report Questionnaire for Sacral Sparing After Spinal Cord Injury

Spinal Cord Injuries Clinical Trial

Official title:
Development and Validation of a Bowel-routine-based Self Report Questionnaire for Sacral Sparing After Spinal Cord Injury

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04951297
Other study ID # BYSY201109
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2013
Est. completion date January 1, 2016

Study information
Verified date June 2021
Source Peking University Third Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To develop a self-administered tool for assessment of sacral sparing after spinal cord injury (SCI) and to test its validity in individuals with SCI.

Recruitment information / eligibility
Status Completed
Enrollment 102
Est. completion date January 1, 2016
Est. primary completion date January 1, 2016
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - patients with SCI Exclusion Criteria: - had neurologic impairments unrelated to SCI, such as peripheral nerve injury, brain injury and cognitive deficits, or if they were unable to complete the questionnaire.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• None, just observation
None ,just observation test

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Peking University Third Hospital

Outcome
Type Measure Description Time frame Safety issue
Primary sacral sparing self-report questionnaire sacral sparing self-report questionnaire 12months
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