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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06339268
Acronym
COGNITION
Enrollment
120
Registered
2024-04-01
Start date
2023-11-01
Completion date
2026-03-01
Last updated
2025-04-24

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

Conditions

Prehabilitation

Brief summary

Postoperative cognitive deficit and its connection with surgery and general anesthesia were first mentioned in the literature in 1955 by Bradford. Cognitive disorders in the postoperative period are postoperative delirium (POD) and postoperative cognitive dysfunction (POCD). POD is an acute dysfunction in cognition, which did not exist preoperatively. Attention deficit disorder is the main symptom of POD and refers to the inability to direct, focus, maintain, or shift attention. Memory impairment, disorientation, or perceptual disturbances may also be present. Cognitive capacity changes in POD patients develop and fluctuate in the first few days after surgery. Unlike POD, there is no formal definition for POCD. Based on data from the existing literature, it is defined as newly diagnosed cognitive deterioration that occurs after surgery. The diagnosis of POCD should be based on pre- and postoperative screening with appropriate psychometric tests. Risk factors for the development of POCD include those related to the surgical procedure, anesthesia, or the patient himself. Compared to less invasive and shorter operations, there is a higher risk of developing POCD after major, invasive, and long-term operations. Additional risk factors are intraoperative (intraoperative bleeding, perioperative transfusion treatment, hypotension) and postoperative complications (respiratory insufficiency, pneumonia, atelectasis, bronchospasm, bronchopleural fistula, and pulmonary edema). Presurgical optimization (Prehabilitation) is a widespread concept that aims to improve the general condition of the patient or optimize comorbidities before major surgery. Prehabilitation is primarily focused on improving physical ability and nutritional status, but it is developing in the direction of a multimodal approach that includes measures to reduce stress and anxiety. Psychological factors are increasingly recognized as an essential element of prehabilitation and are often added to prehabilitation programs. Older patients, who meet the diagnostic criteria for frailty and are at risk of developing postoperative complications such as cognitive function disorders are increasingly undergoing lung resection. These complications can affect the outcome and speed of postoperative recovery.

Detailed description

After setting the indication for operative treatment, patients who meet the criteria for inclusion in the study, after signing the informed consent, will be randomized into two groups: 1. The first group (intervention) where the patient will receive preoperative cognitive stimulation and physical therapy for one month before surgical treatment. 2. The second group (control) where patients receive standard treatment. Randomization will be performed using computer randomization by doctors who do not participate in the testing and preoperative preparation of the patient. Patients included in the first group will be subjected to psychological testing and preoperative training to receive tasks to improve cognitive functions. This technique, known as presurgical cognitive optimization, involves several standardized tests of cognitive stimulation through the cognitive training application (Cognifit) on a phone or tablet that patients use three times a week for 20 minutes for a month (from inclusion in the study to scheduled surgery). Also, after consultation with a physiatrist and testing for the presence of weakness syndrome as well as other tests related to the mobility and physical condition of patients, preoperative physical therapy (breathing exercises, walking, climbing stairs) will be carried out in this group of patients. Patients from this group, in addition to the exercise program they carry out for physical preparation before surgery, receive preoperative education on techniques and exercises that they will do immediately postoperatively in bed. Patients will keep a diary of preoperative activities that will be controlled by researchers. Patients from the second group will be tested perioperatively with cognitive and weakness syndrome tests and other physiatry tests, but without cognitive intervention and physical therapy, they will be referred for surgery.

Interventions

BEHAVIORALCognitive training, CogniFit App

A patient will receive preoperative cognitive stimulation and physical therapy for one month before surgical treatment.

Sponsors

Military Medical Academy, Belgrade, Serbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

After setting the indication for operative treatment, patients who meet the criteria for inclusion in the study, after signing the informed consent, will be randomized into two groups: 1. The first group (intervention) where the patient will receive preoperative cognitive stimulation and physical therapy for one month before surgical treatment. 2. The second group (control) where patients receive standard treatment.

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Postoperative recoveryFrom 1st til 5th postoperative dayAssessment of the speed of recovery - A test of functional recovery: 10 items for assessing basic activities by a six-level ordinal scale 0 (activity not achieved) -5 (fully independent and secure). Total scores can range from 0 to 50 (from inability to perform any activity to complete independence.) Speed of recovery will be assessed with a comparison of the scores during the first 5 postoperative days.
Perioperative depression and anxietyFrom 1 month preoperatively (schedulling patient for surgery) until 30th postoperative dayPerioperative assessment of depression, anxiety, and stress: DAS - depression and anxiety assessment scale (42-item self-report scale measures the negative emotional states of depression, anxiety, and stress) Scoring Guide DASS (42) Scoring Depression Anxiety Stress Normal 0-9 0-7 0-14 Mild 10-13 8-9 15-18 Moderate 14-20 10-14 19-25 Severe 21-27 15-19 26-33 Extremely Severe 28+ 20+ 34+ Results are assessed between the intervention group and control
Postoperative deliriumFirst postoperative dayIncidence of newly diagnosed postoperative delirium: CAM-ICU (Confusion Assessment Method for the ICU) using CAM-ICU Flowsheet: Step 1. Acute Change or Fluctuating Course of Mental Status: yes (delirium positive) or no (CAM-ICU negative) Step 2. Inattention: 0 - 2 errors (CAM-ICU negative) or \> 2 errors go to next step Step 3. Altered Level of Consciousness (the Richmond Agitation-Sedation Scale - RASS): from -5 (unarousable - no response to voice or physical stimulation) to +4 (combative). Anything other than 0 (alert and calm) goes to the next step. Step 4. Disorganized thinking: 0-1 errors (not delirious) or \> 1 error (delirious) Feature 1 plus 2 and either 3 or 4 present = CAM-ICU positive
Functional status and postoperative recoveryFrom 1 month preoperatively (schedulling patient for surgery) until 30th postoperative dayAssessment of the functional status and speed of recovery - Clinical frailty scale: from 1 (very fit) to 9 (terminally Ill). Only patients marked as less than 6 are included in the study. Any change in the assessment score is marked as significant
Postoperative cognitive dysfunctionFrom 1 month preoperatively (schedulling patient for surgery) until 30th postoperative dayIncidence of newly diagnosed or worsening of the existing postoperative cognitive decline assessed by change in score of MMSE - Mini-Mental State Examination (an 11-question measure that tests five areas of cognitive function: orientation, registration, attention, and calculation, recall, and language). On a scale from 0-30 points: ≥ 25 points normal cognitive function 19-24 points minor cognitive dysfunction 10-18 points medium cognitive dysfunction ≤ 9 points major cognitive dysfunction In this study change of 3 or more points in MMSE between two tests ( pre and postoperative) or between individual participants will be marked as significant

Secondary

MeasureTime frameDescription
Overall outcome: MorbidityFrom surgery until 30th postoperative dayMorbidity will be presented as % of patients within the groups who develop any kind of complication or illness postoperatively during the period of follow-up
Overall outcome: MortalityFrom surgery until 30th postoperative dayMortality will be presented as overall and % of deaths in the study population and both groups
Overall outcome: Complication rateFrom surgery until 30th postoperative dayComplication rate will be presented as % of patients within the groups who develop: * Respiratory failure * Pneumonia * Atelectasis * Bronchospasm * Bronchopleural fistula * Air leak * Pulmonary edema

Countries

Serbia

Contacts

Primary ContactVojislava Neskovic, PhD
vojkan43@gmail.com+381641775320
Backup ContactMarija Markovic, MD
markovicmarija@hotmail.com+38162666653

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026