The Efficacy of Electrical Version of Patient Reported Outcome

Status Completed

Clinical Trial Summary

Recently the importance of electrical PRO system is increased for the accuracy, convenience, and efficiency for both patients and physicians. For the evaluation of quality of life, various self-reported questionnaires is filled-out by the patient, mostly in front of outpatient clinic, and doctor usually take times to calculate the score. If there is electrical PRO which is available with mobile device, the efficacy of clinic would be improved. The investigators developed such a system and applied the system for patients with spinal disease. The investigators assessed the effectiveness of application of electrical-PRO in outpatients' clinic for patients who had filled-up same questionnaire in paper version.

Clinical Trial Description

Age, sex, education levels, use of smartphone, the number of applications. ;

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02387073
Study type	Observational [Patient Registry]
Source	Seoul National University Hospital
Contact
Status	Completed
Phase	N/A
Start date	September 2013
Completion date	March 2014

View Details

See also
Status	Clinical Trial	Phase
Recruiting	`NCT05610098` - Gene Expression Profiles in Spinal Tuberculosis.
Recruiting	`NCT04120272` - Discovery for Biomarkers and Risk Factors for Postoperative Delirium in Elderly Patients With Spine Surgery
Terminated	`NCT04174534` - ROMEO®2 PAD. 2 YEARS PROSPECTIVE FOLLOW-UP
Enrolling by invitation	`NCT05181098` - Prospective Robotic-Guided Registry of Spine Surgery
Completed	`NCT05148637` - General Anesthesia and Regional Cerebral Oxygenation inSpine Surgery Prone Position	N/A
Recruiting	`NCT05709782` - Phase II Cohort of Spinal Stereotactic Radiotherapy in Patients Using a MR LINAC	Phase 2
Recruiting	`NCT06407167` - Neuropathic Pain in Patients With Degenerative Lumbar Stenosis
Completed	`NCT04391855` - Wound Infiltration With Tramadol, Dexmedetomidine, or Magnesium Plus Ropivacaine for Pain Relief After Spine Surgery	Phase 4
Not yet recruiting	`NCT06393530` - Erector Spinae Plane Block for Cervical Spine Surgery	Phase 4
Not yet recruiting	`NCT06335095` - Gait Analysis and Degenerative Spine
Enrolling by invitation	`NCT04364295` - Stronger Together Global Registry
Recruiting	`NCT06451588` - Fecal Microbiota Transplantation in Axial Spondyloarthritis	Phase 2
Recruiting	`NCT02809950` - Effects of Preoperative Oral Carbohydrates Loading in Patients at High Risk of Postoperative Nausea and Vomiting Undergoing Spinal Surgery	Phase 4
Recruiting	`NCT04524377` - Evaluation of the Influence of Deep Brain Stimulation on the Spinal Deformities Associated With Parkinson's Disease	N/A
Completed	`NCT02534714` - Analysis of Hypovitaminosis D and Osteopenia/Osteoporosis in Spinal Disease Patients Who Underwent a Spinal Fusion at Illinois Neurological Institute, Peoria, IL., a Retrospective Review From November 1, 2012 to October 31, 2014 and Prospective Pilot From July 1, 2015-June 30, 2016
Terminated	`NCT01458938` - This Study is to Determine if Degenerative Spinal Pain and Disorders Cause the Levels of Substance P to Change in a Patients Saliva, Blood and/or Cerebrospinal Fluid.	N/A
Recruiting	`NCT01642706` - Regulatory B Cells in Inflammatory Rheumatisms and Biomarkers of Response to Biologic Treatments
Recruiting	`NCT04176562` - Prospective SPINE Registry
Recruiting	`NCT03969602` - Cognitive Behavioral Therapy (CBT) After Lumbar Spinal Fusion in Patients With High Pain Catastrophizing	N/A
Recruiting	`NCT04775537` - OssiMend BA in Posterolateral Instrumented Lumbar Fusion