Clinical Trials Directory

Trials / Completed

CompletedNCT04828109

Digital Intervention Postoperative Protocol

A Digital Intervention Protocol to Enhance Recovery After Head and Neck Surgery

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Oregon Health and Science University · Academic / Other
Sex
All
Age
18 Years – 89 Years
Healthy volunteers
Accepted

Summary

Postoperative recovery after head and neck surgery is complex, and often requires utilization of narcotic medications. The aim of this study is to evaluate reduction in pain and use of opioid medications through Virtual Reality (VR) and Fitbit wearable activity devices.

Detailed description

Enhanced Recovery After Surgery (ERAS) protocols were introduced as a method to optimize perioperative patient care. Narcotic medications are frequently utilized in postoperative care, but these have risks including sedation or dependence. Non-pharmacologic measures for postoperative pain control may help limit the need for opioids in postoperative pain control. Early mobilization is also important after surgery, however postoperative mobility is rarely monitored and relies on subjective reports. The investigators will seek to examine the implementation of an ERAS protocol using VR and Fitbit wearable activity devices on postoperative recovery after head and neck surgery. This is a prospective, 4-arm, randomized controlled trial.

Conditions

Interventions

TypeNameDescription
DEVICEVirtual RealityUse of any virtual reality experiences available
DEVICEFitbitUse of a Fitbit wearable activity device to track daily step goals.

Timeline

Start date
2021-10-25
Primary completion
2022-09-01
Completion
2022-09-01
First posted
2021-04-01
Last updated
2023-10-31

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04828109. Inclusion in this directory is not an endorsement.