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临床试验/NCT04134416
NCT04134416已完成3 期

Effects of Combining Donepezil, Intensive Language Rehabilitation and Transcranial Direct Current Stimulation on Language Recovery and Brain Reorganization in Chronic Post-stroke Aphasia

University of Malaga1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2019年1月8日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
20
试验地点
1
主要终点
Communicative Activity Log (CAL)

研究概览

简要总结

Post-stroke aphasia (PSA), the partial or total loss of the ability to produce and/or understand language associated with stroke, is a highly prevalent and disabling disorder that negatively impacts the personal, social and working life of patients and families. Modern theory-based language therapies (LT) with proved efficacy in chronic PSA are brief (weeks), intensive, and oriented to specific domains (e.g., anomia). However, in order to maximize therapeutic benefits, it becomes essential to implement complementary strategies that boost gains in language, communication and behaviour and also to identify predictors of treatment response (demographics, anatomical) that enable to customize interventions adjusting them to each profile (linguistic deficits, brain structure and connectivity). Our group has repeatedly shown that LT combined with cognitive enhancing drugs (CED) (e.g., Donepezil and Memantine) are safe and promote better outcomes that when these interventions are administered separately. Moreover, non-invasive brain stimulation techniques (NIBS), such as transcranial direct current stimulation (tDCS), are also emerging as a promising treatment option for chronic PSA. However, is still unknown whether or not treatments that combine several biological strategies aid to improve outcomes further. Brain changes induced by these interventions and the premorbid characteristic of a "good responder" are also unknown. The aims of this clinical trial are: (1) Study the efficacy of combined treatments in a sample of patients with chronic PSA (n = 40); (2) Document with multimodal neuroimaging the functional and connectivity changes (neuroplasticity) promoted by these interventions; and (3) Identify linguistic, cognitive and behavioural variables that may predict outcomes for each intervention.

详细描述

Aphasia is a devastating disorder involving total or partial loss of language. It can affect all communicative, expressive, and receptive modalities, including language production, comprehension, reading, writing, and the ability to gesture. Stroke is the most common cause of aphasia and its incidence is very high in Europe, varying between 318 and 372 cases in men and between 195 and 240 in women per 100,000 inhabitants. In Spain it is the second cause of death and the first in women, affecting approximately 130,000 people every year. Between 21 and 38% of these cases present post-stroke aphasia (PSA) in the acute stage. PSA is associated with high morbidity and mortality, and only 20% of those affected recover spontaneously. Consequently, PSA is very frequent and evolves to chronicity in most patients. There are different subtypes of aphasia depending on the linguistic profile. A distinction is made between aphasia with preserved repetition and aphasia with altered repetition. The first group includes transcortical aphasias (sensory, motor and mixed) and anomic aphasias, and the second, in order of severity, global aphasias, Wernicke aphasias, Broca aphasias, and Conduction Aphasias (CA). The latter group is associated with perisylvian lesions and are most frequent (>80% of cases). Aphasias in the first 2-3 months tend to evolve into less severe profiles, so that Broca and Wernicke aphasias can, in chronic stages, progress to CA.

Aphasia has a negative impact on the affected person and their family members, reducing work, personal, affective and social life. It is accompanied by high health and social expenditure, since one third of patients are under 65 years of age and cannot return to work due to the inability to communicate. For this reason, the implementation of strategies aimed at improving aphasia, communication, associated emotional disorders and the quality of life of patients and carers is crucial to achieve autonomy, allowing them to return to work and prevent additional cognitive and affective impairment. Currently, the most popular PSA rehabilitation therapies are: speech rehabilitation therapies, drugs and, more recently, non-invasive neurostimulation techniques.

  1. Speech therapies Speech therapy is the treatment of choice in aphasia. The most commonly used is conventional or standard therapy where a specific strategy (description of pictures, repetition of words or phrases, answers to questions) is employed depending on the patient's deficits. They are usually applied 2 or 3 times a week with a duration of 30-45 minutes per session. However, some of the problems with these therapies are their prolonged duration (several years) and, consequently, their high cost, which limits their applicability in Public Health Services. In addition, the logistical limitations (difficulty of transport, shortage of staff) of the treatment centres prevent the administration of the minimum of 2 hours per week of therapy required to obtain clinically relevant benefits. On the other hand, the benefits obtained are insufficient and the progress made decreases once the treatment has been abandoned. For this reason, during the last two decades, speech therapies have been designed in which short (2 weeks) but very intensive (3 hours per day) rehabilitation exercises based on neuroscientific evidence are applied which effectively solve the limitations of traditional therapies. In this sense, Intensive Language-Action Therapy (ILAT) administered for two consecutive weeks (3 hours/day for 2 weeks - 30 hours of treatment -) has gained worldwide acceptance as it is significantly more effective than traditional rehabilitation techniques even when the total therapy time (2 hours/week for 15 weeks - 30 hours of treatment) is the same. In addition, the benefits achieved with ILAT in 2 weeks are maintained for 6 months after completion of treatment. ILAT is a group rehabilitation therapy (2 or 3 participants) that employs a play dynamic among participants, and its ILAT-plus modality also reinforces the training of specific language skills (e.g., repetition).
  2. Pharmacological interventions LT is effective in the PSA, even in chronic stages (> 6 months after stroke). However, in many patients with moderate and severe aphasia the benefits of LT are limited (e.g., partial recovery of verbal fluency and auditory comprehension).These limitations have led to the use of other, more effective interventions to treat PSA. Several clinical trials in patients with acute and chronic PSAs conducted in the last decade have shown that the benefits achieved with rehabilitation can be significantly increased when these therapies are combined with drugs. Several pharmacological agents (Levodopa, Bromocriptine, Piracetam, Amantadine, Dexamfetamine, and others) have been used with variable results. However, several controlled clinical trials have found significant improvements in production deficits, understanding, and in the overall severity of aphasia in patients with PSAs treated with Piracetam, Donepezil, Galantamine, or Memantine. In PSA rehabilitation, biological and behavioral treatments strengthen the activity of perilesional regions and brain areas that previously did not perform language functions, but that after stroke are recruited vicariously increasing the ability of language recovery in the patient. In the last decade, it has been shown that the acetylcholinesterase inhibitor (an enzyme that degrades acetylcholine) Donepezil, and the NMDA receptor antagonist Memantine (antidementia drugs with a good safety/tolerability profile) are more effective than placebo in the treatment of PSA, especially when these are prescribed in association with rehabilitation techniques based on neuroscientific evidence.
  3. Neurostimulation Transcranial direct current stimulation (tDCS) is a non-invasive brain stimulation technique that induces changes in the excitability of brain tissue by increasing (anodal stimulation, A-tDCS) or decreasing (cathodal stimulation, C-tDCS) the activity of nerve cells by applying weak electrical currents. The theoretical justification for the use of tDCS as an adjuvant technique in PSA rehabilitation is based on the fact that it modulates (increases or decreases) the rate of neuronal discharge, presumably through changes in the resting potential of the membrane, and thus facilitates or hinders the functioning of connections between neuronal groups. tDCS has been shown to be effective in a variety of neurological and psychiatric disorders and has several advantages over other stimulation techniques, e.g. transcranial magnetic stimulation: better safety profile, easy to use, well tolerated by patients and better cost-benefit ratio. Increasingly, studies indicate that tDCS has beneficial effects on language deficits (verbal fluency, naming, grammatical decision) in people with PSA. In addition, when applied in conjunction with ST, it enhances the benefits obtained in PSA. Benefits have been described in patients with PSA using varied stimulation parameters (intensity, type, duration, brain area), each with different theoretical justification. The main modalities are (1) anodal stimulation (A-tDCS; excitatory) of perilesional areas with the aim of promoting the recovery of brain tissue surrounding the lesion; (2) cathodal stimulation (C-tDCS inhibitory stimulation of healthy regions interfering with recovery); (3) A-tDCS on areas of the healthy hemisphere to increase activity and facilitate the reorganization of functions that previously depended on injured areas of the left hemisphere. tDCS is a technique that has been shown to be effective, although more studies are needed leading to the identification of the most suitable stimulation parameters, the location-extent of the lesion, the previous brain structure of each patient, and to determine the added value that this technique provides in combination therapies.

Justification and project contributions Intensive ST, neurostimulation and pharmacological interventions have independently been shown to be effective in the rehabilitation of PSA. Previous work indicates that combination therapies (ILAT and drug therapy) are superior to other treatment options as they enhance synergistic mechanisms that promote improved learning, language and functional communication in affected individuals. However, more research is needed to explore the benefits of combination therapies (e.g. Donepezil, ILAT and tDCS) and to identify the mechanisms and structures that are modulated by each of these rehabilitation therapies and that mediate recovery, with the aim of establishing response predictors.

The aim of the current project is to evaluate the efficacy of ILATplus (ILAT + repetition/imitation training) (3 hours/day for 2 consecutive weeks, total = 30 hours) combined with Donepezil and tDCS in the treatment of cognitive deficits in patients with chronic post-stroke aphasias, with a special emphasis on Conduction Aphasia (CA).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

This is an open label except for the tCDS treatment which is double blind (AtDCS vs shamtDCS).

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 18 and 70 years
  • Right handedness (80 point in the Edinburgh Handedness Inventory)
  • Spanish as native language
  • Single left-hemisphere stroke
  • Diagnosis of aphasia established by a score in the Aphasia Quotient of the Spanish version of the Western Aphasia Battery (WAB) < 93.8 points.

排除标准

  • Dysarthria without aphasia
  • Multiple or bilateral injuries
  • Increased risk of a new stroke or unstable neurological condition (e.g. transient ischemic attacks)
  • History of severe psychiatric illness (schizophrenia, major depression, bipolar disorder, anxiety disorders)
  • Alcohol and substance use or abuse
  • Coexistence of aphasia with dementia.

研究组 & 干预措施

Anodal transcranial direct current stimulation

Experimental

Transcortical direct current stimulation (tDCS) will be applied using a STARSTIM neurostimulation device (Neuroelectrics, Barcelona). Each participant will receive 10 20-minute sessions while receiving REGIAplus (online). Group 1 will receive active stimulation (anodal stimulation, A-tDCS).The active electrode will be placed in the region of the lower right frontal rotation and the reference electrode in the extraencephalic zone (left clavicle). Combined rehabilitation sessions (REGIAplus/tDCS) will be conducted, as indicated above, in weeks 9 and 10 of the trial.

干预措施: Donepezil (Drug)

Anodal transcranial direct current stimulation

Experimental

Transcortical direct current stimulation (tDCS) will be applied using a STARSTIM neurostimulation device (Neuroelectrics, Barcelona). Each participant will receive 10 20-minute sessions while receiving REGIAplus (online). Group 1 will receive active stimulation (anodal stimulation, A-tDCS).The active electrode will be placed in the region of the lower right frontal rotation and the reference electrode in the extraencephalic zone (left clavicle). Combined rehabilitation sessions (REGIAplus/tDCS) will be conducted, as indicated above, in weeks 9 and 10 of the trial.

干预措施: Intensive-Language Action Therapy (Behavioral)

Anodal transcranial direct current stimulation

Experimental

Transcortical direct current stimulation (tDCS) will be applied using a STARSTIM neurostimulation device (Neuroelectrics, Barcelona). Each participant will receive 10 20-minute sessions while receiving REGIAplus (online). Group 1 will receive active stimulation (anodal stimulation, A-tDCS).The active electrode will be placed in the region of the lower right frontal rotation and the reference electrode in the extraencephalic zone (left clavicle). Combined rehabilitation sessions (REGIAplus/tDCS) will be conducted, as indicated above, in weeks 9 and 10 of the trial.

干预措施: Transcranial direct current stimulation (Device)

Sham transcranial direct current stimulation

Sham Comparator

Group 2 will receive sham stimulation (S-tDCS). In the sham stimulation, the same helmet and electrode that is used in the active stimulation will be placed but, in this case, we will apply only a slight current at the beginning and end of the session with the objective of simulating the effects that are experienced with the active stimulation without producing significant cortical stimulation. The active electrode will be placed in the region of the lower right frontal rotation and the reference electrode in the extraencephalic zone (left clavicle). Combined rehabilitation sessions (REGIAplus/tDCS) will be conducted, as indicated above, in weeks 9 and 10 of the assay.

干预措施: Donepezil (Drug)

Sham transcranial direct current stimulation

Sham Comparator

Group 2 will receive sham stimulation (S-tDCS). In the sham stimulation, the same helmet and electrode that is used in the active stimulation will be placed but, in this case, we will apply only a slight current at the beginning and end of the session with the objective of simulating the effects that are experienced with the active stimulation without producing significant cortical stimulation. The active electrode will be placed in the region of the lower right frontal rotation and the reference electrode in the extraencephalic zone (left clavicle). Combined rehabilitation sessions (REGIAplus/tDCS) will be conducted, as indicated above, in weeks 9 and 10 of the assay.

干预措施: Intensive-Language Action Therapy (Behavioral)

Sham transcranial direct current stimulation

Sham Comparator

Group 2 will receive sham stimulation (S-tDCS). In the sham stimulation, the same helmet and electrode that is used in the active stimulation will be placed but, in this case, we will apply only a slight current at the beginning and end of the session with the objective of simulating the effects that are experienced with the active stimulation without producing significant cortical stimulation. The active electrode will be placed in the region of the lower right frontal rotation and the reference electrode in the extraencephalic zone (left clavicle). Combined rehabilitation sessions (REGIAplus/tDCS) will be conducted, as indicated above, in weeks 9 and 10 of the assay.

干预措施: Transcranial direct current stimulation (Device)

结局指标

主要结局

Communicative Activity Log (CAL)

时间窗: Each participant/ main carer will be evaluated at week 0 (baseline), 8, 10 and 26.

To assess communicative behavior in the everyday life of patients. Changes from Baseline in CAL scores at 8, 10 and 26 weeks. Minimum and maximum values: 0-90 points (0-40 points for quality of communication; 0-40 points for amount of communication). Higher values mean better outcome.

Western Aphasia Battery (WAB)

时间窗: Each participant will be evaluated at week 0 (baseline), 8, 10 and 26.

To assess major clinical aspects of language function: information content, fluency, auditory comprehension, repetition and naming. Changes from Baseline in Western Aphasia Battery scores at 8, 10 and 26 weeks. Minimum and maximum values: 0-100 points. Higher scores mean better outcome.

Stroke Aphasia Depression Questionnaire (SADQ-10)

时间窗: Each participant/ main carer will be evaluated at week 0 (baseline), 8, 10 and 26.

To assess depressive symptomatology in persons with post-stroke aphasia. Changes from Baseline in SADQ-10 scores at 8, 10 and 26 weeks. Minimum and maximum scores: 1-30 points. Lower values mean better outcome.

Stroke and Aphasia Quality of Life Scale 39 (SAQOL-39)

时间窗: Each participant/ main carer will be evaluated at week 0 (baseline), 8, 10 and 26.

To assess Quality of Life in persons with post-stroke aphasia. Changes from Baseline in SAQOL-39 scores at 8, 10 and 26 weeks. Minimum and maximum scores: 1-85 (Physical scale); 1-35 (Communication scale); 1-55 (Psychosocial scale); 1-20 (Vitality scale); 1-5 (Total mean scale). Higher values mean better outcome.

次要结局

  • Mini Mental State Examination (MMSE)(Each participant will be evaluated at week 0 (baseline).)
  • Raven´s Colored Progressive Matrices (RPM), set A, B & AB(Each participant will be evaluated at week 0 (baseline).)
  • Starkstein Apathy Scale (SAS).(Each participant/ main carer will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Catastrophic Reaction Scale (CRS)(Each participant/ main carer will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Trail-Making Test, parts A & B (TMT)(Each participant will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Cognitive Reserve Questionnaire.(Each participant will be evaluated at week 0 (baseline))
  • Hospital Anxiety and Depression Scale (HADS).(Each participant/ main carer will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Neuropsychiatric Inventory (NPI).(Each participant/ main carer will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Repetition of clichés and novel sentences (experimental test)(Each participant will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Visual Dynamic Analogue Scale (D-VAMS).(Each participant will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Visual-analogue test assessing anosognosia for language impairment (VATA-L)(Each participant/ main carer will be evaluated at week 0 (baseline), 8, 10 and 26)
  • Communicative Effectiveness Index (CETI)(Each participant/ main carer will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Queens List for the Naming of Stimuli (experimental test)(Each participant will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Non-Verbal Oral Apraxia Screening Test (experimental test)(Each participant will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Cognition test for Patients with Aphasia (experimental test)(Each participant will be evaluated at week 0 (baseline).)
  • Digit Span Test from the Wechsler Adult Intelligence Scale (WAIS)(Each participant will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Attention Network Test (ANT).(Each participant will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Neurobehavioral Change after Aphasia Scale (experimental test).(Each participant/ main carer will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Barthel Index (IB)(Each participant/ main carer will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE)(Each participant/ main carer will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • The Apraxia of Speech Rating Scale (ASRS).(Each participant will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Corsi Block Tapping Test from the Wechsler Adult Intelligence Scale (WAIS)(Each participant will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Batería para la Evaluación de los Trastornos Afásicos (BETA). Battery for the Evaluation of Aphasia Disorders. Subscale 1,2,6,13,14,21 & 26.(Each participant will be evaluated at week 0 (baseline), 8, 10 and 26.)
  • Queens List for the Repetition of Stimuli (experimental test)(Each participant will be evaluated at week 0 (baseline), 8, 10 and 26.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Marcelo Luis Berthier

Full Professor

University of Malaga

研究点 (1)

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