Trials / Unknown
UnknownNCT03337178
Fitbit Pilot Study in Post-operative Lumbar Degenerative Spinal Stenosis Patients
Fitbit Pilot Study to Increase Physical Activity and Overall Health in Post-operative Lumbar Degenerative Spinal Stenosis Patients
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- The London Spine Centre · Academic / Other
- Sex
- All
- Age
- 60 Years
- Healthy volunteers
- Not accepted
Summary
Spinal stenosis is a common orthopedic spine condition that limits individuals ability to walk and stand because of nerve compression. Surgical treatment can alleviate leg pain and improve function such as increasing physical activity. This study will use Fitbit technology to monitor patient's post-operative physical activity. It will evaluate the efficacy of a Fitbit incentive based walking program on improving post-operative physical activity and rehabilitation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BEHAVIORAL | Blinded Fitbit | Fitbit is worn for 3 months post-operatively with no activity feedback or step goals |
| BEHAVIORAL | Fitbit | Fitbit is worn for 3 months post-operatively with feedback and step goals |
Timeline
- Start date
- 2018-08-01
- Primary completion
- 2022-08-31
- Completion
- 2022-12-31
- First posted
- 2017-11-08
- Last updated
- 2020-08-21
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT03337178. Inclusion in this directory is not an endorsement.