Clinical trial · Interventional
A Digital Intervention Protocol to Enhance Recovery After Head and Neck Surgery
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This trial studies examines the impact of virtual reality (VR) experiences and Fitbit wearable activity devices on postoperative recovery after head and neck surgery. Virtual reality has shown to help rehabilitation and pain control primarily in non-surgical fields, and researchers are interested in using this to help postoperative pain control. Early mobilization after surgery is also important, and may increase lung capacity, improve gastrointestinal function, reduce pain, and reduce risk of deep venous thrombosis. Use of virtual reality and Fitbit devices may improve postoperative pain control and reduce narcotic use among hospitalized patients after head and neck surgery.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Head and Neck Carcinoma | Head and Neck Carcinoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Fitbit | Device | — | UNRESOLVED |
| Questionnaire Administration | Other | — | UNRESOLVED |
| Virtual Reality Device | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (4)
- type
- EXPERIMENTAL
- label
- Group 1 (VR, Fitbit)
- description
- Beginning postoperative day 1, patients use VR over 30 minutes up to 4 times daily on weekdays and 2 times daily on weekends, and wear Fitbit daily with a goal of 2,000 steps until the day of discharge, or until 14 days after surgery. Pre and post-VR pain scores will be obtained for each VR use. Sleep data may also be evaluated from Fitbit devices.
- interventionNames
- Device: Fitbit
- Other: Questionnaire Administration
- Device: Virtual Reality Device
- type
- EXPERIMENTAL
- label
- Group 2 (VR)
- description
- Beginning postoperative day 1, patients use VR over 30 minutes up to 4 times daily on weekdays and 2 times daily on weekends until the day of discharge or until 14 days after surgery. Pre and post-VR pain scores will be obtained for each VR use.
- interventionNames
- Other: Questionnaire Administration
- Device: Virtual Reality Device
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 89 Years
Show eligibility criteria text
Inclusion Criteria: * English speaking (Ability to interact with virtual reality content may be impacted by inability to understand English) * Older than 18 years of age and younger than 89 years of age. Both men and women and members of all races and ethnic groups will be included * Planned to undergo major surgery at Oregon Health \& Science University (OHSU) with the Department of Otolaryngology-Head and Neck Surgery with an expected length of stay (LOS) of 2 days or more * Ability to understand and the willingness to sign a written informed consent document Exclusion Criteria: * Planned postoperative admission to the intensive care unit (ICU) * Social or psychiatric conditions that may interfere with compliance * Isolation precautions * Complex head and neck procedure requiring resection or reconstruction involving the scalp, orbit, or mid-face. This would limit the ability to utilize the VR headset * Reconstruction, incisions, wounds, wound care, or injury that impact the ability to place on the VR headset or wear a Fitbit device around the wrist. This would limit the ability to utilize the VR headset or the Fitbit device * History of seizure or epilepsy * History of vertigo or persistent dizziness * Use of cardiac pacemaker, requirement for hearing aid on at all times, or have defibrillators * Limitations that impair mobility. This would limit the ability to utilize the Fitbit device * Use of a walker or wheelchair at baseline. This would limit the ability to utilize the Fitbit device * Children * Pregnant women * Neonates of uncertain viability or nonviable neonates * Decisionally impaired adults * Prisoners
References
Publications (0)
Data not yet available