Trial · NCT07901985
A Rehabilitation Data Collection Study in Patients With Spinal Cord Injury
NCT07901985, Recruiting, Seoul National University Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. A Rehabilitation Data Collection Study in Patients With Spinal Cord Injury. Trials, record NCT07901985. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07901985
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- A Rehabilitation Data Collection Study in Patients With Spinal Cord Injury
- NCT number
- NCT07901985
- Status
- Recruiting
- Enrollment
- 250 participants, estimated
- Lead sponsor
- Seoul National University Hospital
- Conditions
- Spinal Cord Injuries (SCI)
- First posted
- 2026-10-28
- Last updated
- 2026-10-28
Source ClinicalTrials.gov
Registered outcomes15
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Level of disability (WHODAS 2.0 total score) | Phase1. Baseline survey (at admission) / Phase2. Follow-up survey 1 (approximately 6 months post-discharge) / Phase3. Follow-up survey 2 (approximately 12 months post-discharge) | Level of disability is measured using the World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0). The summary score ranges from 0 to 100, with higher scores indicating greater disability (a worse outcome). |
| Other | Demographic information | Phase1. Baseline survey (at admission) / Phase2. Follow-up survey 1 (approximately 6 months post-discharge) / Phase3. Follow-up survey 2 (approximately 12 months post-discharge) | Name, sex, date of birth, resident registration number, nationality, marital status, education level, region of residence, economic activity (employment) status, occupational category |
| Other | Injury-related information | Phase1. Baseline survey (at admission) | Age at injury, date of injury, mode of transfer after injury, place of residence at the time of injury |
| Other | Neurological status (ISNCSCI) | Phase1. Baseline survey (at admission) | Neurological impairment classified with the International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI), reported as the ASIA Impairment Scale (AIS) grade (A = complete to E = normal). |
| Other | Pain intensity (0-10 numeric rating scale) | Phase1. Baseline survey (at admission) / Phase2. Follow-up survey 1 (approximately 6 months post-discharge) / Phase3. Follow-up survey 2 (approximately 12 months post-discharge) | Pain intensity measured with a Numeric Rating Scale (NRS), ranging from 0 (no pain) to 10 (worst imaginable pain); higher scores indicate worse pain. |
| Other | Spasticity severity (0-10 numeric rating scale) | Phase1. Baseline survey (at admission) /Phase2. Follow-up survey 1 (approximately 6 months post-discharge) / Phase3. Follow-up survey 2 (approximately 12 months post-discharge) | Spasticity severity rated on a 0-10 numeric scale, where 0 indicates no spasticity and 10 indicates the most severe spasticity; higher scores indicate worse spasticity. |
| Other | Functional ambulation (FAC) | Phase1. Baseline survey (at admission) | Walking ability classified with the Functional Ambulation Category (FAC), ranging from 0 to 5; higher categories indicate more independent walking (better outcome). |
| Other | Hand function (Jebsen-Taylor Hand Function Test) | Phase1. Baseline survey (at admission) | Hand function measured with the Jebsen-Taylor Hand Function Test (JHFT), reported as time to complete the tasks in seconds; shorter time indicates better function. |
| Other | Independence in activities of daily living(SCIM III) | Phase1. Baseline survey (at admission) | Functional independence measured with the Korean version of the Spinal Cord Independence Measure III (K-SCIM-III). Total score ranges from 0 to 100; higher scores indicate greater independence (better outcome). |
| Other | Depression (PHQ-9) | Phase1. Baseline survey (at admission) / Phase2. Follow-up survey 1 (approximately 6 months post-discharge) / Phase3. Follow-up survey 2 (approximately 12 months post-discharge) | Depressive symptoms measured with the Patient Health Questionnaire-9 (PHQ-9). Total score ranges from 0 to 27; higher scores indicate more severe symptoms (worse outcome). |
1 to 10 of 15Source ClinicalTrials.gov
See all 15 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07901985
GET https://conductscience.org/api/trials/v1/NCT07901985/registered