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Objective Assessment of Activity and Sleep Quality In Burst Spinal Cord Stimulation

NCT02950831 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 27

Last updated 2019-08-29

Study results available
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Summary

The purpose of this study is to assess feasibility of using wearable sensors to capture objective assessments of patient's activity and sleep quality during the spinal cord stimulation (SCS) treatment continuum.

Conditions

Interventions

OTHER

Accelerometry

Record of activity levels using a wrist worn accelerometer

Sponsors & Collaborators

  • AZ Sint-Augustinus, Wilrijk

    collaborator UNKNOWN

  • AZ Middelheim, Antwerpen

    collaborator UNKNOWN

  • Erasmus Medical Center

    collaborator OTHER

  • Abbott Medical Devices

    lead INDUSTRY

Principal Investigators

  • Lalit Venkatesan, Ph.D. · Abbott Medical Devices

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-10-31
Primary Completion
2018-03-31
Completion
2018-03-31

Countries

  • Belgium
  • Netherlands

Study Locations

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Entities

Diseases
Companies

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 NCT02950831 on ClinicalTrials.gov