Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01141647 · ClinicalTrials.gov registry record · NA
SCI-VIP: Predictive Outcome Model Over Time for Employment (PrOMOTE)
A NA study of Spinal Cord Injuries, sponsored by VA Office of Research and Development.
- Completed
- Registry status
- NA
- Development phase
- 1,047
- Enrollment target
- 7
- Study locations
NCT01141647: Completed NA study of Spinal Cord Injuries, sponsored by VA Office of Research and Development.
NCT01141647 is a NA study of Spinal Cord Injuries that has completed, run by VA Office of Research and Development. The registered enrollment target is 1,047 participants, above the 56-participant average among 202 other Spinal Cord Injuries trials with a reported enrollment target (1770% higher). The trial reports 7 study locations across 6 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01141647, a NA study of Spinal Cord Injuries, has completed, sponsored by VA Office of Research and Development.
- COMPLETED
- Registry status
- NA
- Development phase
- 1,047 participants
- Enrollment target
- 7
- Study locations
Study Summary
This study will be an extension of the Spinal Cord Injury Vocational Integration Program (SCI-VIP). The study involves research about how to help Veterans with spinal cord injury (SCI) gain employment. Vocational rehabilitation is a special field of service aimed at putting persons with disabilities in the best possible position to become employed. The Veterans Administration has a long history of providing vocational rehabilitation for Veterans with mental health issues and has recently started providing similar services to persons with physical disabilities, including SCI. Past research has shown that vocational rehabilitation is effective in helping some Veterans with spinal cord injury (SCI) gain employment. The extension of this work through PrOMOTE study will establish a large national database of over 2000 Veterans with SCI, containing extensive employment, medical, functional and psychosocial data. The study will analyze both quantitative and qualitative measures to maximize its findings.
Primary Outcome
To model the probability of obtaining CE, we first dichotomized CE as 'yes' or 'no'. The Competitive Employment Rate is reported in Outcome Measure 2. We then used unconditional logistic regression to model the probability of obtaining CE through a univariate modeling approach to determine statistically significant predictors of CE. Statistically significant predictors at the p\<0.10 criterion level were then explored in a final multivariate model. Demographic (age, race, marital status, etc.),
Conditions Studied
Interventions
- BEHAVIORAL Vocational Rehabilitation
Study Locations (7)
Texas
- VA North Texas Health Care System Dallas VA Medical Center, Dallas, TX - Dallas
- Michael E. DeBakey VA Medical Center (152) - Houston
California
- VA Palo Alto Health Care System, Palo Alto, CA - Palo Alto
Florida
- James A. Haley Veterans' Hospital, Tampa, FL - Tampa
Massachusetts
- VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA - Boston
Ohio
- VA Medical Center, Cleveland - Cleveland
Virginia
- Hunter Holmes McGuire VA Medical Center, Richmond, VA - Richmond
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,047 participants |
| Start Date | 2011-08 |
| Est. Completion | 2015-03 |
| Phase | NA |
What the finished NCT01141647 record still lists
NCT01141647 is an interventional study that assigns participants to a tested intervention. Its 1,047 participants enrollment target places it among the larger protocols in the corpus, above the 56-participant average among 202 other Spinal Cord Injuries trials with a reported enrollment target (1770% higher).
The record links to 1 condition, with Spinal Cord Injuries appearing as the primary indexed condition, and to 1 intervention - of which Vocational Rehabilitation is the first listed.
NCT01141647 lists 7 locations in 6 states (Texas, California, Florida).
Frequently Asked Questions
What is clinical trial NCT01141647 about?
NCT01141647 is a clinical study titled "SCI-VIP: Predictive Outcome Model Over Time for Employment (PrOMOTE)". This study will be an extension of the Spinal Cord Injury Vocational Integration Program (SCI-VIP). The study involves research about how to help Veterans with spinal cord injury (SCI) gain employment. Vocational rehabilitation is a special field of service aimed at putting persons with disabilities...
What is the current status of trial NCT01141647?
This trial is currently completed. It is a NA study. The enrollment target is 1,047 participants. The study started on 2011-08. Estimated completion is 2015-03.
What conditions does trial NCT01141647 study?
This clinical trial studies the following conditions: Spinal Cord Injuries.
What interventions are being tested in trial NCT01141647?
The interventions under investigation include: Vocational Rehabilitation (BEHAVIORAL).
Who is sponsoring clinical trial NCT01141647?
This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01141647 being conducted?
This trial has 7 study locations across California, Florida, Massachusetts, Ohio, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Spinal Cord Injuries
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT01141647's enrollment target sits among peer trials
1,047 1st of 202 higher than 202 of 202 other Spinal Cord Injuries trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Spinal Cord Injuries trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
Feasibility of the BrainGate2 Neural Interface System in Persons With Tetraplegia (BG-Speech-02)
RECRUITING · NA
-
Closed-loop Spinal Stimulation for Restoration of Upper Extremity Function After Spinal Cord Injury
RECRUITING · NA
-
Neuromodulation to Improve Respiratory Function in Cervical Spinal Cord Injury
RECRUITING · NA
-
Transcutaneous Spinal Stimulation and Exercise for Locomotion
RECRUITING · NA
-
HAPPINESS: cHAnging the Perceived Pain INtEnSity in Populations With Spinal Cord Injury and With Health Disparities: A Feasibility Study
RECRUITING · NA
-
Dosing rTMS for Depression Post-SCI
RECRUITING · NA
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT06717347 · 1,046 participants · Phase 3
A Study to Evaluate Zilovertamab Vedotin (MK-2140) Combination With Rituximab Plus Cyclophosphamide, Doxorubicin, and Prednisone (R-CHP) Versus Rituximab Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-CHOP) in Participants With Previously Untreated DLBCL (MK-2140-010)
- NCT04505618 · 1,050 participants · NA
Optical Coherence Tomography Angiography in Subjects With Retinal Vascular Disease
- NCT04511806 · 1,050 participants
Childhood Cancer Predisposition Study (CCPS)
- NCT05028972 · 1,050 participants · NA
Hearing Impairment, Strategies and Outcomes in VA Emergency Departments
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia