Trials / Completed
CompletedNCT02950831
Objective Assessment of Activity and Sleep Quality In Burst Spinal Cord Stimulation
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 27 (actual)
- Sponsor
- Abbott Medical Devices · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Detailed description
Eligible patients will undergo standard clinical care using BurstDR SCS and will be asked to wear a wrist worn accelerometer for a baseline period, during SCS trial and for 3 months after activation of the SCS stimulation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Accelerometry | Record of activity levels using a wrist worn accelerometer |
Timeline
- Start date
- 2016-10-01
- Primary completion
- 2018-03-01
- Completion
- 2018-03-01
- First posted
- 2016-11-01
- Last updated
- 2019-08-29
- Results posted
- 2019-08-29
Locations
3 sites across 2 countries: Belgium, Netherlands
Source: ClinicalTrials.gov record NCT02950831. Inclusion in this directory is not an endorsement.