Abstract

Background Traditionally, people with aphasia (PWA) are treated with impairment-based language therapy to improve receptive and expressive language skills. In addition to language deficits, PWA are often affected by some level of working memory (WM) impairments. Both language and working memory impairments combined have a negative impact on PWA's quality of life. The aim of this study was to investigate whether the application of intermittent theta-burst stimulation (iTBS) combined with computerized WM training will result in near-ransfer effects (i.e., trained WM) and far-transfer effects (i.e., untrained language tasks) and have a positive effect on the quality of life of PWA. Methods The participant was a 63-year-old Greek-Cypriot male who presented with mild receptive aphasia and short-term memory difficulties. Treatment was carried out using a multiple baseline (MB) design composed of a pretherapy or baseline testing phase, a therapy phase, and a posttherapy/follow-up phase. The treatment program involved iTBS application to the left dorsolateral prefrontal cortex (DLPFC), an area responsible for WM, for 10 consecutive sessions. The participant received a 3-minute iTBS application followed by 30-minute computer-assisted WM training. Outcome measures included a WM screening test, a standardized aphasia test, a nonverbal intelligence test, story-telling speech samples, a procedural discourse task, and a questionnaire addressing quality of life. These measures were performed three times before the treatment, immediately upon completion of the treatment, and once during follow-up testing at 3 months posttreatment. Results We found a beneficial effect of iTBS and WM training on naming, reading, WM, reasoning, narrative, communication efficiency, and quality of life (QoL). Implications for Rehabilitation. Noninvasive brain stimulation combined with computerized WM training may be used in aphasia rehabilitation to improve WM and generalize to language improvement.

Highlights

  • Transcranial magnetic stimulation (TMS) is a noninvasive technique of brain neuromodulation and neurostimulation [1] which produces a brief electric current in the coil to generate a magnetic field, and in turn, it activates neurons in the vicinity of the coil

  • These studies reported significant improvements in global cognition and memory when measured with the following neuropsychological tests: Alzheimer’s Disease Assessment Scale-cognitive (ADAS-Cog), Mini Mental State Exam (MMSE), Addenbrooke Cognitive Examination (ACE), Apathy Evaluation Scale (AES-C), Blessed Dementia Scale (BDS), Clinical Global Impression (CGI), Clinical Global Impression of Change (CGIC), Digit Symbol Substitution Test (DSST), Montreal Cognitive Assessment (MOCA), Neuropsychiatric Inventory (NPI), Rey Auditory Verbal Learning Test (RAVLT), Trail Making Test (TMT), and Zarit Burden Scale (ZBS)

  • We report improvement in memory, fluid intelligence, language, and quality of life (QoL) after 10 sessions of intermittent theta-burst stimulation (iTBS) combined with computerized working memory (WM) training in a single case study with no adverse effects during treatment and at follow-up periods

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Summary

Introduction

Transcranial magnetic stimulation (TMS) is a noninvasive technique of brain neuromodulation and neurostimulation [1] which produces a brief electric current in the coil to generate a magnetic field, and in turn, it activates neurons in the vicinity of the coil. The aim of this study was to investigate whether the application of intermittent theta-burst stimulation (iTBS) combined with computerized WM training will result in near-ransfer effects (i.e., trained WM) and far-transfer effects (i.e., untrained language tasks) and have a positive effect on the quality of life of PWA. Outcome measures included a WM screening test, a standardized aphasia test, a nonverbal intelligence test, story-telling speech samples, a procedural discourse task, and a questionnaire addressing quality of life. These measures were performed three times before the treatment, immediately upon completion of the treatment, and once during follow-up testing at 3 months posttreatment.

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