Fitbit for Postoperative Ambulation
Completed · Not applicable
Conditions studied: Postoperative Care
In brief
This trial will investigate whether using reminder alarms with a wireless activity tracking device (Fitbit) will increase daily ambulation in individuals who have just had colorectal surgery.
Key facts
- Study ID
- NCT02833324
- Run by
- Emory University
- People needed
- 48
- Starts
- 2016-07-01
- Expected to finish
- 2016-12-01
- Last updated by the study team
- 2017-10-17
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Undergoing an elective surgical procedure in colorectal services at Emory University Hospital
You may not qualify if…
- Post-surgical admission into the intensive care unit (ICU)
- Have an open abdomen due to surgical complications
- Wound Vacuum Assisted Closure (VAC) dependent
Where it is running
- Emory University Hospital — Atlanta, Georgia, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.