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Clinical Study on Optimizing the Cognitive Function of Elderly Patients in the Perioperative Period by Virtual Reality Technology.

Research and Application of Intelligent Devices for Optimizing the Cognitive Function of Elderly Patients in the Perioperative Period through Virtual Reality Technology.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096765
Enrollment
Unknown
Registered
2025-02-06
Start date
2025-02-15
Completion date
Unknown
Last updated
2025-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Function

Interventions

VR group:Three days before the operation, VR intervention training was carried out on the experimental group.
Control group:Routine preoperative self-regulation

Sponsors

Stomatological Hospital Affiliated to Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
55 Years to 89 Years

Inclusion criteria

Inclusion criteria: 1. Elderly patients aged between 55 and 89 years old who need to undergo oral and maxillofacial surgery. 2. Elderly patients have sufficient cognitive and motor abilities to complete the VR cognitive assessment. 3. Elderly patients have no eye diseases, no serious underlying diseases, and no vertigo. 4. Elderly patients sign the informed consent form for participating in the experiment, have complete medical record information, actively cooperate with various tasks in the VR intervention, and abide by the regulation..

Exclusion criteria

Exclusion criteria: 1.Severe and uncorrectable visual and auditory impairments; impaired upper limb function, severe motor disorders caused by spinal disorders, etc. 2.Some underlying diseases that increase the risk of postoperative delirium (PND), such as anemia and diabetes as indicated in relevant literature. 3.Neuropathic diseases like photosensitive epilepsy or delirium. 4.Patients with an expected lifespan of less than 6 months, a history of mental or neurological disorders (including depression, severe central nervous system depression, schizophrenia, epilepsy, Parkinson's disease or Alzheimer's disease), and major impairments (such as blindness, severe deafness, or dementia that may interfere with cognitive tests) are excluded. 5.Patients who use psychotropic drugs or opioids, have a history of delirium, or have a history of alcoholism or withdrawal within the past 6 months are excluded.

Design outcomes

Primary

MeasureTime frame
Cognitive function;

Secondary

MeasureTime frame
Delirium;Delirium;Adverse reactions during the use of VR;post-operative conditions;General information of the patient;Intraoperative conditions;

Countries

China

Contacts

Public ContactChao Zhang

Stomatological Hospital Affiliated to Chongqing Medical University

632769033@qq.com+86 158 2317 2321

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026