NCT02616406CompletedNot Applicable
Assessment of Physical Activity to Determine When Patients Return to Baseline Levels of Activity Following Outpatient Inguinal Hernia Surgery
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Mayo Clinic
- Enrollment
- 5
- Locations
- 1
- Primary Endpoint
- Determine time of return to baseline activity following elective outpatient hernia repair using wearable accelerometers that measure physical movement.
Study Overview
Brief Summary
This is a study using wearable monitoring devices, patient activity and sleep patterns to monitor pre and post operative following outpatient inguinal hernia surgery to determine when these parameters return to baseline.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to 80 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Patients presenting for outpatient inguinal hernia repair without significant medical comorbidities
- •Patients who consent to participating and willing to wear device for designated time period per protocol
Exclusion Criteria
- •History of chronic opioid use
- •Inability to speak English
- •Inability to give informed consent
Outcomes
Primary Outcomes
Determine time of return to baseline activity following elective outpatient hernia repair using wearable accelerometers that measure physical movement.
Time Frame: 8 weeks
Secondary Outcomes
- Determine pain levels on visual analog scale after outpatient hernia repair via telephonic questionnaire.(8 weeks)
Investigators
Karl A. Poterack, M.D.
Principal Investigator
Mayo Clinic
Study Sites (1)
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