MedTrace Logo

Feasibility and Acceptability of ReCognitionVR-based Cognitive Stimulation in Surgical Patients

NCT06232317 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2025-09-17

Study results available
· View outcomes & findings →

Summary

This study aims to assess the feasibility, acceptability, and safety of using ReCognitionVR virtual reality-based software in older surgical patients. Results from this study will be used to inform the design of a future study in critically ill hospitalized patients at risk for delirium.

Conditions

  • Surgery
  • Delirium
  • Delirium, Post-Operative

Interventions

OTHER

Virtual Reality Software

The ReCognitionVR virtual reality software is delivered via an Oculus Quest 2 device. This three-dimensional simulated software was designed to improve attention and executive functions.

OTHER

Traditional Orientation Methods

Standard-of-care methods to orient patients after surgery

Sponsors & Collaborators

  • National Institute on Aging (NIA)

    collaborator NIH

  • The Methodist Hospital Research Institute

    lead OTHER

Principal Investigators

  • Hina Faisal, MD · The Methodist Hospital Research Institute

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-12-09
Primary Completion
2024-03-21
Completion
2024-05-07

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06232317 on ClinicalTrials.gov