MedPath

Patient Ambulation in Post-Op Recovery

Not Applicable
Completed
Conditions
Physical Activity
Interventions
Device: RX Navigait
Registration Number
NCT02528669
Lead Sponsor
Intermountain Health Care, Inc.
Brief Summary

The purpose of this study is to create a platform that accurately measures and reports patient physical activity before a procedure, during the hospital stay, and after discharge from the hospital.

Detailed Description

Early ambulation in post-operative patients has shown benefits including shorter length of stay and/or fewer complications. Accelerometers have been found as useful instruments in encouraging ambulation in patients. Accelerometers are non-invasive devices that can evaluate changes in movement, gait, and ambulatory activity. Although these devices can be beneficial, little research exists on the best way to engage patients in ambulation, how to develop a standard ambulation protocol, and the best algorithms to measure ambulation post-operation. This study seeks to develop a standardized activity tracker and program that will encourage patient ambulation and allow patients and healthcare providers to view the progress of daily walking goals.

A total of 3,000 patients will be asked if they would like to participate in this study. A healthcare provider will explain to the patient the benefits of getting out of bed, sitting, and walking after an invasive procedure. Patients who decide to participate will be given an accelerometer during their pre-operation visit or after their surgery while still in the hospital. Patients will be asked to wear the accelerometer continuously during waking hours. The accelerometer will provide patients with daily walking goals, reminders of when it is time to walk, track step count, record time of walk, and duration of walk. Patients will be asked to wear the accelerometer until their post-op visit (about 30 days).

The following data points will be analyzed:

* Relationship between ambulation and patient outcomes

* Relationship between ambulation and other health factors

* Effectiveness of prototype platform to motivate and monitor patient activity

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
52
Inclusion Criteria
  • Patients of physician study investigators
Exclusion Criteria
  • Patients whose physicians find they are unfit to participate in a walking program

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
RX NavigaitRX NavigaitIndividuals in this group will be given an activity tracking device that receives and displays walking reminders and daily walking goals. In addition, they will be given additional education about the benefits of walking. The device will track daily steps taken, minutes of walking, and frequency of walking bouts throughout the day.
Primary Outcome Measures
NameTimeMethod
Patient Ambulation (number of steps, frequency, time)Up to 3 months
Secondary Outcome Measures
NameTimeMethod
Accuracy of accelerometer algorithms measuring post operation walkingUp to three years
Number of patients completing ambulation programUp to three years

Trial Locations

Locations (1)

Intermountain Medical Center

🇺🇸

Murray, Utah, United States

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