Telehealth Postop Follow up RCT
Status unconfirmed · Not applicable
Conditions studied: Patient Satisfaction
In brief
A randomized controlled trial that will evaluate whether telephone two-week postoperative follow up visits are an acceptable and safe alternative to traditional face-to-face-clinic two-week postoperative visits.
Key facts
- Study ID
- NCT03791697
- Run by
- Jackson, Elisha
- People needed
- 142
- Starts
- 2018-07-09
- Expected to finish
- 2019-07-31
- Last updated by the study team
- 2019-01-03
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Women >18 desiring surgical management of prolapse or incontinence
- English speaking
- Willing and able to provide written and informed consent without assistance from medical surrogate or interpreter
- Immediate access to telephone services (landline, mobile phone, office phone)
You may not qualify if…
- Women <18
- Non-English speaking
- Unwilling and unable to provide written and informed consent without assistance from surrogate or interpreter
- Hearing impairment
- No access to telephone services (landline, mobile phone, office phone)
- Grade 3 complication- a complication requiring surgical, endoscopic, or radiological intervention. [3]
- Patient who did not attend any postoperative follow up visit
Where it is running
- University of Florida Health — Tampa, Florida, United States (enrolling)
Full record on ClinicalTrials.gov
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