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Clinical Trials/NCT02549560
NCT02549560CompletedNot Applicable

Effects of the Transcranial Direct Current Stimulation on Prevention of Cognitive Dysfunction in Elderly Patients Submitted to Cardiac Surgeries: Prospective, Randomized and Double-blind Study

University of Sao Paulo1 site in 1 country138 target enrollmentStarted: July 8, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
138
Locations
1
Primary Endpoint
tDCS as a cognitive enhancer for patients with postoperative cognitive dysfunction after cardiac surgery

Study Overview

Brief Summary

Postoperative cognitive dysfunction (POCD) is a contrary event observed between 20 to 83%, especially on elderly and patients submitted to cardiac surgery. The prevention and rehabilitation on cases of POCD can improve the quality of life and decrease the mortality in surgical patients. The effect of the noninvasive cerebral stimulation, also known as transcranial Direct Current Stimulation (tDCS) has been studied to be used in the treatment of brain injuries and depression, and also in the cognitive rehabilitation. The hypothesis is that the use of the tDCS technique can decrease the occurrence of POCD and cognitively rehabilitate patients submitted to cardiac surgeries.

Detailed Description

SUMMARY Postoperative cognitive dysfunction (POCD) is a contrary event observed between 20 to 83%, especially on elderly, patients submitted to cardiac surgery. Besides the difficult diagnosis, the limitations of prevention and rehabilitation on cases of POCD may compromise the quality of life and increase the mortality in surgical patients. The neuromodulator effect of the noninvasive cerebral stimulation, also known as transcranial stimulation, with a low intensity electric current (tDCS) has been studied to be used in the treatment of brain injuries and depression, and also in the cognitive rehabilitation. The hypothesis is that the use of the tDCS technique in sessions can decrease the occurrence of POCD and cognitively rehabilitate patients submitted to cardiac surgeries. The objective of this study is to evaluate the effect of the tDCS over the occurrence of POCD on patient submitted to cardiac surgeries with cardiopulmonary bypass (CPB)

After the approval by the constitutional ethics commission, will be included in the study 138 adult patients submitted to a cardiac surgery. After the subscription of the consent form by the responsible the patients will be randomly allocated in two groups:

tDCS GROUP: These patients will be submitted to 2 daily sessions of cerebral stimulation, starting from the first day after the surgery, for 4 consecutive days, with each session having 20 minutes, and a minimum break of 8 hours between them. Will be applied a direct current stimulus of 2 milliampere (mA) in the right anode and in the left cathode on the prefrontal right region.

CONTROL GROUP: In these patients will be applied, with the same equipment used in tDCS, a simulated stimulus similar to the active one. They will also be submitted to some psychological test to evaluate theirs mnemonics, attentional, executive and global functions. The volunteers will be evaluated in a model with the intention to treat (ITT) of recovering the cognitive functions evaluated by scores on the test based on normative tables, this is the primary outcome. The secondary outcome will be improvements on the response of these cognitive tests, the admission of these patients will last 15 days in the intensive treatment unity and in the hospital. There will also be evaluated data relative to the surgery, the cognitive evolution and the quality of life in postoperative period.

Will also be applied neuropsychological tests to evaluate memory, attention, and executive functions as well as another tests to assess specifics contents useful to describe the sample and research' results.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Adult patients over 18 years candidates do cardiac surgeries with extracorporeal circulation. Patients that signed the Free and Clarified Consent Form

Exclusion Criteria

  • •Historic of progressive mental disease or dementia
  • •Psychiatric disease that affects cognition
  • •Lack of fluency of the Portuguese language
  • •Historic of epilepsies, convulsions, fainting and syncope
  • •With serious cranial traumas, carriers of ventriculoperitoneal derivation valves or metallic objects implanted in the brain
  • •With hearing problems or cochlear implants
  • •With cardiac pacemaker or any metallic implants in the body; Use of neuropsychiatric medications on the preoperative period
  • •Already submitted to the stimulation of the tDCS

Arms & Interventions

tDCS GROUP

Active Comparator

These patients will be submitted to 2 daily sessions of cerebral stimulation, starting from the first day after the surgery, for 4 consecutive days, with each session having 20 minutes, and a minimum break of 8 hours between them. Will be applied a direct current stimulus of 2 milliampere (mA) in the right anode and in the left cathode on the prefrontal right region.

Intervention: tDCS (Device)

CONTROL GROUP

Sham Comparator

In these patients will be applied, with the same equipment used in tDCS, a simulated stimulus similar to the active one. They will also be submitted to some psychological test to evaluate theirs mnemonics, attentional, executive and global functions.

Intervention: tDCS (Device)

Outcomes

Primary Outcomes

tDCS as a cognitive enhancer for patients with postoperative cognitive dysfunction after cardiac surgery

Time Frame: 18 months

Evaluate if tDCS sessions decrease the occurrence of POCD in patients submitted to extracorporeal circulation on cardiac surgery. Neuropsychological testing: Changes in results from neuropsychological assessment pre (before the first stimulation) to post treatment (after the last stimulation). There will be a eight days time frame from pre assessment to post assessment. The improvement of the skills and cognitive functions will be compare with results of tests for evaluation of quality of life, depressive symptoms and neuropsychological battery to assess, attention, visuospatial perception, immediate memory, operational, long-term memory and executive skills and recall, including processing speed.

Secondary Outcomes

  • Changes in results from neuropsychological assessment pre (before the first stimulation) to post treatment (after the last stimulation).(15 days)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Livia Stocco Sanches Valentin

Ph.D.

University of Sao Paulo

Study Sites (1)

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