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Effect of preoperative multimodal brain function-guided cognitive training on postoperative delirium and its neurological mechanisms in elderly patients undergoing major non-cardiac surgery: a prospective randomized controlled trial

Effect of preoperative multimodal brain function-guided cognitive training on postoperative delirium and its neurological mechanisms in elderly patients undergoing major non-cardiac surgery: a prospective randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124662
Enrollment
Unknown
Registered
2026-05-15
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

Postoperative delirium

Interventions

Cognitive training group:From the time of enrolment, patients will use the ‘Light of the Future’ mobile app to undergo preoperative digital cognitive training. They should train for at least two hours
Control group (routine care group):Routine preoperative preparation and standardized anesthesia management

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Patients aged over 65 who are scheduled to undergo elective major non-cardiac, non-neurological surgery under general anaesthesia (with an expected duration of more than 2 hours); (2) Have signed an informed consent form; (3) Are able to communicate fluently in Chinese

Exclusion criteria

Exclusion criteria: 1) Life expectancy of less than 6 months; (2) Patients with a history of psychiatric or neurological disorders, such as depression, severe central nervous system depression, schizophrenia, epilepsy, Parkinson’s disease, delirium or Alzheimer’s disease; (3) Patients who are unable to undergo cognitive testing due to blindness, severe deafness, communication difficulties or dementia; (4) Patients routinely taking psychotropic or opioid medications prior to surgery; (5) Patients who have experienced any cerebrovascular event within the past three months, such as a stroke or transient ischaemic attack; (6) Patients with a history of alcohol abuse or withdrawal within the past six months; (7) Patients currently participating in other clinical trials; (8) Patients scheduled to undergo a second surgical procedure within seven days of the planned surgery.

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative delirium (POD);

Secondary

MeasureTime frame
Severity and duration of POD;Short-term (1 month) and long-term (6 months) cognitive function scores following surgery;Incidence of postoperative complications, length of hospital stay, and all-cause mortality at 30 days and 6 months;Neuroimaging measures (fMRI functional connectivity strength, DWI white matter integrity);Electrophysiological measures (ERP latency/amplitude, resting-state power spectrum);

Countries

China

Contacts

Public ContactFang Panpan

The First Affiliated Hospital of Anhui Medical University

fangpanpan2020@126.com+86 157 5518 1289

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026