Adverse cerebral effects of anaesthesia on old people.
P D BEDFORD
https://pubmed.ncbi.nlm.nih.gov/13243706/Actively Recruiting
Led by Military Medical Academy, Belgrade, Serbia · Updated on 2025-04-24
120
Participants Needed
1
Research Sites
17 weeks
Total Duration
This research focuses on elderly patients undergoing lung resection surgery and aims to evaluate ways to prevent postoperative cognitive problems such as delirium and cognitive dysfunction. These issues can arise after surgery and general anesthesia, especially in older adults who are frail or have complications. The study explores how preoperative cognitive and physical preparation may affect recovery and cognitive outcomes after major surgery. Participants will be randomly assigned to one of two groups. The intervention group will receive cognitive training using a mobile application called Cognifit three times a week for 20 minutes over one month before surgery. They will also undergo physical therapy including breathing exercises, walking, and stair climbing, plus education on postoperative exercises to do in bed. The control group will receive standard care without the cognitive or physical prehabilitation. During the study, participants will be assessed before surgery and up to 30 days after surgery for cognitive function, delirium, anxiety, depression, and physical recovery. Researchers will use psychological tests, weakness syndrome assessments, and functional status evaluations. Patients will keep diaries of their preoperative activities. The study will also monitor complications, morbidity, and mortality up to 30 days post-surgery to understand overall outcomes and recovery patterns.
CONDITIONS
Cognitive and Physical Optimization in Prevention of Postoperative Cognitive Deficit in Elderly With Lung Resection
V
Vojislava Neskovic, PhD
M
Marija Markovic, MD
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Military Medical Academy, Belgrade, Serbia
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 month
Participants in the intervention group receive preoperative cognitive stimulation using a cognitive training app and physical therapy exercises to prepare for surgery. Participants in the control group receive standard care without these preoperative interventions.
Approximately 12 sessions of cognitive training (3 times per week) plus physical therapy activities
Duration - Day of surgery
Participants undergo lung resection surgery.
1 visit (in-person surgery)
Duration - 30 days
Participants are monitored for cognitive function, delirium, depression, anxiety, functional status, and recovery during the first 30 days following surgery.
Visits and assessments during 1 to 5 days post-surgery and follow-up visits until day 30
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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P D BEDFORD
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https://pubmed.ncbi.nlm.nih.gov/34257192/Military Medical Academy, Belgrade, Serbia
Lead Sponsor