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Completed

NCT Number: NCT06608316

Intermittent Theta-burst Stimulation for Mild Cognitive Impairment

The objectives of this study are to:

1. Evaluating the Impact of iTBS on Cognitive and Physical Functions: The investigators will investigate the efficacy of intermittent theta burst stimulation (iTBS) in patients with mild cognitive impairment (MCI), focusing on its effects on dual-task walking abilities, balance abilities, and cognitive function. 2. Comparing Clinical Efficacy Based on Stimulation Sites: The investigators will compare the clinical efficacy of iTBS targeting the left dorsolateral prefrontal cortex (DLPFC) versus bilateral DLPFC stimulation. This comparison aims to directly examine potential differences in therapeutic outcomes based on the site of stimulation. 3. Investigating Neurophysiological Mechanisms: The investigators plan to elucidate the neurophysiological mechanisms underlying the improvements in cognitive functions and dual-task walking abilities in MCI patients facilitated by iTBS. This will be achieved using fNIRS neuroimaging of brain activity.

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Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Hong Kong Polytechnic University

Hong Kong, 000000

About this study

Mild cognitive impairment (MCI) is a syndrome characterized by cognitive decline that is greater than expected with normal aging; however, it is not severe enough to meet dementia criteria. Accordingly, MCI is considered a transitional state between normal aging and dementia, with a high risk of progression to Alzheimer's disease (AD). In MCI, memory and other cognitive domains such as executive function and visuospatial skills are typically affected. Furthermore, people with MCI have impaired dual-task walking function, decreased balance, and an increased risk of falls compared to cognitively normal older adults, thus affecting the ability to perform daily activities. Moreover, sleep disturbances, such as reduced efficiency and disruptions, are common in MCI, which exacerbates cognitive decline and accelerates the progression to dementia.

Non-invasive brain stimulation (NIBS) techniques have shown potential for enhancing both cognitive and functional outcomes in neuropsychiatric diseases. Transcranial magnetic stimulation (TMS) is the most common form of NIBS, which modulates cortical excitability and neuroplasticity by inducing electromagnetic pulses in targeted brain regions. TMS can be delivered in various forms based on frequency and intervals. Intermittent theta burst stimulation (iTBS) is a type of patterned TMS that mimics endogenous theta rhythms. It has shown cognitive benefits in healthy populations as well as those with AD, depression, and other conditions, but evidence regarding its efficacy in MCI is limited.

While interventions like dual-task training and non-invasive brain stimulation (e.g., tDCS) have shown promise in mitigating dual-task coordination impairments, research specifically focusing on the impact of iTBS on dual-task walking abilities in MCI patients remains scarce. Further research is needed to explore the potential of iTBS to improve dual-task walking ability, balance, and fall prevention in MCI populations.

Although the dorsolateral prefrontal cortex (DLPFC) is often targeted with NIBS due to its role in executive functions, comparisons of bilateral versus unilateral left DLPFC stimulation have not been conducted in MCI. Overall, there is a lack of empirical evidence supporting the use of iTBS protocols to improve cognition and functional activities in MCI. Elucidating the neurophysiological mechanisms underlying NIBS techniques like iTBS remains imperative.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Aged≥65 years;
  • Patient-reported subjective cognitive decline and the total score of the Hong Kong version of Montreal Cognitive Assessment (HK-MoCA) was between 19 and 25;
  • Intact daily functioning in ADL scales and being independent in daily living, and ability to walk at least for 1 minute independently without an assistive device;
  • No serious visual or hearing impairment and can complete relevant assessment and testing;
  • Signed informed consent of patients and their families for iTBS treatment.

Exclusion criteria

  • Identified with contraindications in the rTMS screening questionnaire;
  • Cognitive dysfunction due to craniocerebral trauma or neurological diseases;
  • Presence of severe physical illnesses such as speech disorders or unstable cardiac arrhythmias;
  • Currently in a critical condition such as fever, infection, or organ failure;
  • Significant damage to the left frontal lobe cortex;
  • Currently taking antidepressants or psychostimulants;
  • Unstable vital signs or organ failure;
  • Neuropsychiatric comorbidity or affective disorder that could affect the test results;
  • Patients with dementia.

Treatment and study plan

Intermittent Theta Burst Stimulation

Device

A novel transcranial magnetic stimulation protocol called intermittent theta pulse stimulation (iTBS) effectively mimics the brain's naturally occurring theta rhythms and promotes significant synaptic changes. Compared to traditional stimulation methods, iTBS is more effective at initiating long-term potential (LTP) and produces significant excitatory effects in a shorter period of time.

Primary outcomes

  1. Dual-task cost in cognition (Reaction time)

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    Reaction time will be measured during dual-task conditions

  2. Dual-task cost in gait (gait speed)

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    Gait speed under dual-task condition will be recorded

  3. Dual-task cost in cognition (Accuracy)

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    Accuracy will be measured during dual-task conditions

Secondary outcomes

  1. Blood oxygenation level changes of the brain

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    Blood oxygenation level changes will be measured using Functional Near-Infrared Spectroscopy during dual-task conditions

  2. Dual-task gait performance 1 (gait variability)

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    Gait variability will be measured during dual-task walking

  3. Dual-task gait performance 2 (stride length)

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    Stride length will be measured during dual-task walking

  4. Dual-task gait performance 3 (walking distance)

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    Walking distance will be measured during dual-task walking

  5. Dual-task gait performance 4 (gait cadence)

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    Gait cadence will be measured during dual-task walking

  6. Dual-task gait performance 5 (trunk stability)

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    Trunk stability will be measured during dual-task walking

Other outcomes

  1. Hong Kong Montreal Cognitive Assessment (HK-MoCA)

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    Hong Kong Montreal Cognitive Assessment (HK-MoCA) will be used to global cognitive function, with total points from 0-30. Higher points indicate better performance.

  2. N-back test

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    N-back test will be used to assess executive function.

  3. Modified-Wisconsin Card Sorting Test

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    Modified-Wisconsin Card Sorting Test will be used to assess executive function.

  4. Hong Kong List Learning Test (HKLLT)

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    The Hong Kong List Learning Test (HKLLT) will be used to assess memory function.

  5. Brief assessment of prospective memory (short form).

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    A brief assessment of prospective memory (short form) will be used to assess memory function.

  6. Timed Up and Go test

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    Timed Up and Go test will be used used to assess mobility.

  7. Single Leg Stance test

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    Single Leg Stance test will be used used to assess balance ability.

  8. Pittsburgh Sleep Quality Index

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    The Pittsburgh Sleep Quality Index will be used to assess sleep quality. Each item is scored from 0 to 3, with a total score of 0 to 21. A higher total score indicates poorer sleep quality.

  9. Depression, Anxiety, and Stress Scale (DASS-21)

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    The Depression, Anxiety, and Stress Scale (DASS-21) will be used to assess mental health. It contains 21 items divided into three dimensions, with seven items in each dimension. Scores for each dimension range from 0 to 42, with higher scores representing higher levels of depression, anxiety, and stress.

  10. Physical Activity Scale for the Elderly (PASE)

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    The Physical Activity Scale for the Elderly (PASE) will be used to assess physical activity. There is no set range for the total PASE score; usually a higher score represents a higher level of physical activity.

  11. Fall incidence

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    Monthly telephone interviews for recording fall incidence.

  12. Hong Kong Lawton Instrumental Activities of Daily Living Scale (HKLIADL)

    Time frame: before the initiation of treatment, after 3 weeks of treatment, 4 weeks after termination of the treatment

    Hong Kong Lawton Instrumental Activities of Daily Living Scale (HKLIADL) will be used to assess the ability of Instrumental Activities of Daily Living, with total points from 0-27. Higher points indicate better performance.

Sponsors and collaborators

Lead sponsor

The Hong Kong Polytechnic University

Other

Registry information

Official study title

Optimizing Intermittent Theta-burst Stimulation for Enhancing Dual-Task Walking, Cognitive, and Physical Function in Mild Cognitive Impairment: A Randomized Double-Blind Controlled Trial

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Sep 23, 2024
Registry last updated
Sep 17, 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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