Actively Recruiting

Phase Not Applicable
Age: 60Years +
All Genders
ID06339268

Effects of Preoperative Cognitive and Physical Optimization in the Prevention of Postoperative Cognitive Deficit in Elderly Patients With Lung Resection

Led by Military Medical Academy, Belgrade, Serbia · Updated on 2025-04-24

120

Participants Needed

1

Research Sites

17 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Brief Title

Cognitive and Physical Optimization in Prevention of Postoperative Cognitive Deficit in Elderly With Lung Resection

Who Can Participate

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Older than 60 years
  • Elective lung resection operations
  • Patients who can use a phone or tablet
  • Patients who agreed to participate in the study
  • Clinical scale of weakness less than 6
  • The American Society of Anesthesiologists (ASA) status I, II, III, IV
Not Eligible

You will not qualify if you...

  • Under 60 years of age
  • Significant psychiatric comorbidity (schizophrenia, depression, alcoholism)
  • Significant neurological comorbidity (dementia, cerebrovascular insult in the last 6 months, parkinsonism)
  • Patient's refusal to participate in the study
  • The inability of the patient to use a tablet or phone
  • The American Society of Anesthesiologists (ASA) status V and VI
  • Clinical weakness scale 6 and above

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Run-in Period

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

Surgery

Duration - Day of surgery

Participants undergo lung resection surgery.

1 visit (in-person surgery)

Post-operative Follow-up

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

Trial Site Locations

Total: 1 location

1

Military Medical Academy

Belgrade, Serbia, 11000

Actively Recruiting

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Research Team

V

Vojislava Neskovic, PhD

M

Marija Markovic, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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Published Research Related To This Trial

An update on cognitive frailty: Its definition, impact, associated factors and underlying mechanisms, and interventions.

Taiki Sugimoto, Hidenori Arai, Takashi Sakurai

https://pubmed.ncbi.nlm.nih.gov/34882939

Effect of preoperative cognitive and physical optimization in the prevention of postoperative cognitive deficit in elderly patients with lung resection - cognition trial.

Vojislava Neskovic, Marija Markovic, Nebojsa Maric...

https://pubmed.ncbi.nlm.nih.gov/41387902