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NCT Number: NCT07332169

The Efficacy of Non-invasive Brain Stimulation on Cognitive Functions in Patients With Chronic Obstructive Pulmonary Disease: Double-Blinded Randomised Controlled Trial

The goal of this clinical trial is to examine if non-invasive brain stimulation (NIBS) can enhance cognitive function with chronic obstructive pulmonary disease (COPD) population. The main questions it aims to answer are:

* What is the possibility effect of using the NIBS on cognitive functions as well as the cardiopulmonary parameters in COPD population? * What is the relation between cognitive function parameters and cardiopulmonary parameters in COPD population who suffer from cognitive impairment (CI)? Researchers will compare NIBS to a sham-NIBS to see if NIBS works to improve cognitive function in COPD population.

Participants will:

Receive NIBS or a sham-NIBS 5 sessions/week for 3 weeks for 20 min each session.

Visit the clinic at the beginning for baseline assessment then after the completion of the 3 weeks to reassess them.

Outcome measures for cognitive parameters and pulmonary parameters will be taken pre and post NIBS intervention

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Key information

About this study

  • With over 3.2 million fatalities worldwide, chronic obstructive pulmonary disease (COPD) is considered the third most common cause of mortality and a potentially fatal illness.
  • Due to anomalies in the lung architecture, COPD is characterised by a variety of respiratory symptoms.
  • Cognitive impairment (CI) is one of the problems caused by COPD that extends beyond the respiratory system.
  • The quality of life, treatment compliance, and declines in the condition of COPD patients were all negatively impacted by CI.
  • As of right now, no intervention has been promised to improve CI in patients with COPD.

Objective:

To find out how well non-invasive brain stimulation (NIBS), a novel technique, affects cognitive performance in COPD patients

Methods:

  • Both the participants and the outcome assessor will be in a double-blind RCT.
  • King Fahad University Hospital will be the source of the entirely voluntary participants.
  • The IRB of the Imam Abdulrahman bin Faisal institutions accepted the study protocol.
  • Following an evaluation using the Montreal Cognitive Assessment Test (MoCA), participants will be divided into four groups based on GOLD: mild GOLD 1, moderate GOLD 2, severe GOLD 3, and very severe GOLD 4.
  • For three weeks, both groups will participate in five NIBS sessions per week. While the control group will receive sham brain stimulation, the experimental group will receive active brain stimulation.
  • Both groups will undergo the evaluation before and after the treatment sessions.
  • Primary outcome measurements are battery cognition tests; secondary measures include ABGs, ultrasonography, and cardiopulmonary exercise tests.
  • Independent t-tests will be applied to evaluate the differences between the two groups.
  • The study will use a two-way repeated measures Analysis of Variance (ANOVA) to determine the intervention's efficacy.
  • The association between the improvement of cognitive function and certain factors will be ascertained via the Pearson correlation coefficient.
  • The significance level will be set at a p-value of less than 0.05.

Significant:

  • We hope that the findings of this study will serve as a helpful guide when deciding how to improve CI in patients with COPD and enhance the treatment strategy for this group.
  • The findings of this study will investigate whether NIBS, which is beneficial in another population, can enhance cognitive function in individuals with COPD.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult age from eighteen years old and above.
  • Patients with confirmed COPD via pulmonary function test (PFT) according to the classifications of GOLD.
  • All stages of GOLD will be included
  • Stable patients, which means they were not admitted to the hospital in the last 3 months
  • Patients with COPD with confirmed cognitive impairment by MoCA test.
  • All MoCA stages will be included.

Exclusion criteria

  • Patients without COPD
  • Unstable patients with several admission in the last 3 months
  • Patients with COPD but without cognitive impairment.
  • COPD patients who suffered from any neurological problems
  • COPD patients who are contraindicated for using brain stimulation like psychiatric disorders.

Treatment and study plan

Non-invasive brain stimulation

Device

Non-invasive brain stimulation (NIBS) modifies brain activity without surgery using electric currents. - Transcranial alternating current stimulation (tACS) is one type of NIBS that modifies neuronal oscillations in the brain by applying alternating electrical currents to the scalp through electrodes. - This method can enhance motor abilities, improve cognitive functions, and be used in rehabilitation. - It does this by entraining neurones, which synchronise their firing to the applied sinusoidal frequency. Gamma-Transcranial Alternating Current Stimulation (tACS) of 2 mA at 40 Hz will be given to the experimental group.

Other names: NIBS

Sham Non-Invasive brain stimulation

Device

Non-invasive brain stimulation (NIBS) modifies brain activity without surgery using electric currents. - Transcranial alternating current stimulation (tACS) is one type of NIBS that modifies neuronal oscillations in the brain by applying alternating electrical currents to the scalp through electrodes. - This method can enhance motor abilities, improve cognitive functions, and be used in rehabilitation. - It does this by entraining neurones, which synchronise their firing to the applied sinusoidal frequency. The electric current used as ramps down 60 seconds after the stimulation begins.

Other names: NIBS

Primary outcomes

  1. The battery of neurocognitive tests

    Time frame: At enrolment as baseline assessment and at the end of treatment at 3 weeks

    • Neuropsychological tests are going to be utilised to evaluate cognitive function. • The two key domains to be evaluated are memory and attention. • The Flanker Task will test the attention domain by examining how well the executive control network can be modulated by focusing on one stimulus while concurrently preventing the detection of another stimulus. • The Memory Automaticity Task will be used to evaluate working memory, requiring participants to complete Sternberg-style memory searches in order to attain automaticity; Recalling the existence of a specific letter in the memory set and accurately classifying it are prerequisites for this task. - The previously trained researcher will administer the test.

Secondary outcomes

  1. Cardiopulmonary exercise test (CPET)

    Time frame: At enrolment as baseline assessment and at the end of treatment at 3 weeks

    • The gold standard exercise test for calculating VO2 max is the cardiopulmonary exercise (CPET). • It will be used to evaluate COPD patients' functional capacity and VO2max. Each subject will be assessed using incremental CPET at maximal effort. • The modified Bruce procedure will be used to conduct the test on a treadmill. • Breath-by-breath analysis will be used to evaluate the following gas-exchange and ventilation measurements: VO2, end-tidal pressures for carbon dioxide and oxygen (PETCO2 and PETO2), ventilatory equivalents for carbon dioxide (VE/VCO2), and minute ventilation (VE). - The previously trained researcher will administer the test.
  2. Transcranial Doppler (TCD) ultrasound

    Time frame: At enrolment as baseline assessment and at the end of treatment at 3 weeks

    • Transcranial Doppler (TCD) ultrasound allows for the real-time monitoring of cerebrovascular haemodynamic and blood flow parameters throughout the brain's basal arteries. - Taking into account both the end-diastolic and peak systolic flow velocities, the mean flow velocity (MFV) is calculated, and a few important intracranial arteries are evaluated using the temporal bone window. - Qualified neurologists and vascular technologists will conduct the exam.
  3. Arterial blood gas analysis (ABGs)

    Time frame: At enrolment as baseline assessment and at the end of treatment at 3 weeks

    • The acid-base balance and arterial blood oxygenation are measured by arterial blood gas analysis (ABGs), which uses blood drawn from an artery. • We shall test the arterial carbon dioxide tension (PCO2), arterial blood gas oxygen tension (PO2), and pH. • Patients requiring oxygen will be assessed while using their typical inspiratory oxygen fraction. * The test will be done as part of a hospital's routine.

Other outcomes

  1. Montreal Cognitive Assessment (MoCA) Test

    Time frame: Stratification outcome measure only at the beginning of the study

    • MoCA was employed as a stratification result measure at the start of the enrolment process. * MoCA is used to examine various cognitive areas to detect participants' cognitive impairment (CI). * MoCA test scores range from zero to 30, with a score of more than 26 considered CI. * The previously trained researcher will administer the test.

Study contacts

Contact information is provided by the study sponsor or research team.

Shahad Alkandari, Master's degree

CONTACT

[email protected]

+96597533309

Sponsors and collaborators

Lead sponsor

Shahad Abdulrahman Alkandari

Other Gov

Collaborators

  • Imam Abdulrahman Bin Faisal University

Registry information

Acronym: NIBS COPD

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Jan 12, 2026
Registry last updated
Jan 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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