Mobile Decision Support System for Nurse Management of Neuromodulation Therapy

NCT02474459 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 123

Last updated 2020-06-05

No results posted yet for this study

Summary

The purpose of this study is to test the use of a clinical decision support tool for postoperative care of Parkinson's disease patients who are treated using deep brain stimulation (DBS). The central hypothesis is that the use of a DBS clinical decision support system for individual patient management will enable considerable time savings and reduced burden on patients and caregivers.

Conditions

Interventions

DEVICE

iPad-Based Clinical Support Care

Subjects in this treatment arm will receive deep brain stimulation (DBS) programming at regular intervals as part of routine clinical care. DBS stimulation programming will be done with the use of a iPad-based decision support system.

OTHER

Standard Clinical Care

Subjects in this treatment arm will receive DBS programming at regular intervals as part of routine clinical care.

Sponsors & Collaborators

  • University of Florida

    collaborator OTHER
  • National Institute of Nursing Research (NINR)

    collaborator NIH
  • Wake Forest University Health Sciences

    collaborator OTHER
  • Baylor College of Medicine

    collaborator OTHER
  • NYU

    collaborator UNKNOWN
  • University of California, San Francisco

    collaborator OTHER
  • University of Utah

    lead OTHER

Principal Investigators

  • Christopher Butson, PhD · University of Utah Scientific Computing and Imaging Institute

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-07-31
Primary Completion
2020-04-29
Completion
2020-04-29

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02474459 on ClinicalTrials.gov