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临床试验/NCT05443633
NCT05443633招募中不适用

Enhancing Language Function in Aphasia Using Behavioral Language Intervention

University of Arizona1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2022年10月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
30
试验地点
1
主要终点
Mean change from baseline scores on the naming task

研究概览

简要总结

Aphasia is an acquired impairment of language, that commonly results from damage to language areas in the brain (typically the left side of the brain). This impairment is seen in many aspects of language, including understanding, speaking, reading and writing. It is estimated that about 2 million individuals are currently living with aphasia in the United States. Further, about 200,000 Americans acquire aphasia every year (National Aphasia Association, 2020). Aphasia poses significant impact on the affected individuals and their families. Behavioral treatments that target language deficits have been shown to enhance overall communication skills and life satisfaction among individuals with aphasia. Although there is evidence that suggests that treatment is efficacious for individuals with aphasia, the extent of improvement long-term coupled with the neural patterns among those individuals are largely unknown. The current study aims to investigate the efficacy of language-based treatment and its corresponding neural patterns.

详细描述

The purpose of this study is to develop semantic-based treatment to address language deficits in individuals with acquired language disorders. We propose to develop an individually optimized semantic-based protocol for strategy implementation and word finding facilitation among individuals with language disorders.

Phase 1: Following screening, participants who fulfill the inclusion criteria and have consented to participate in the study will undergo baseline cognitive and language assessment, electroencephalography (EEG) recording and the magnetic resonance imaging (MRI) scan. Participants with language disorders will proceed to the following phases.

Phase 2: After baseline assessment, participants will undergo individualized language treatment in which they will learn semantically- or phonologically based strategies to facilitate word finding difficulties, sentence formulation, or challenges in their narration and discourse. The level at which the treatment will be administered will depend on the participants' level of performance determined by the results of the language and cognitive testing done at baseline. Treatment will be administered twice a week for 10 weeks.

Phase 3: Directly following treatment, patients will undergo cognitive and language assessment, EEG recording, and an MRI scan. This is done to test for short-term changes in behavioral abilities and neural patterns.

Phase 4: After 2 months after the treatment, participants will undergo cognitive and language assessment, EEG recording, and an MRI scan. This final phase of testing is done to test for long-term changes in behavioral abilities and neural responses.

研究设计

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

盲法说明

The subject codes will be used for blinding of the participants, care-providers, and assessors

入排标准

年龄范围
21 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Present with speech-language impairment (aphasia) caused by stroke or dementia
  • •A medical diagnosis of primary progressive aphasia (PPA) by a neurologist or physician
  • •Are native speakers of English
  • •Present with no contraindications for MRI
  • •Have adequate (normal or corrected to normal) vision and hearing

排除标准

  • •Individuals diagnosed with mood, anxiety, psychotic or substance abuse disorders.
  • •Individuals with highly magnetizable metallic implants, including certain dental work, may be excluded due to image quality in MRI.
  • •Individuals with other neurological disorders besides the ones of interest for the study (e.g., epilepsy, Multiple Sclerosis, Parkinson's Disease)
  • •Individuals with contraindications for MRI. This includes but is not limited to pacemakers, metallic cardiac pumps, valves, magnetic materials such as surgical clips, implanted electronic perfusion pumps, or any other condition that would preclude proximity to a strong magnetic field.
  • •Individuals suffering from clinically significant claustrophobia
  • •Severe systemic disease (e.g., renal failure)
  • •Poor overall health
  • •Individuals who are pregnant
  • •Individuals with a history of epileptic activity in the past 12 months
  • •Individuals with a personal or family history of epilepsy or other seizure disorders will not be included in the study.
  • •Individuals who have had a brain surgery in the past
  • •Individuals with implanted metallic skull plates or intracranial implants
  • •Individuals with skin lesions or skull damage
  • •Individuals who have a history of excessive use of alcohol or drugs
  • •Individuals with premorbid psychiatric disease affecting communication
  • •Individuals with severe non-linguistic cognitive disturbances impeding language therapy

研究组 & 干预措施

Active therapy group

Experimental

Participants will undergo individualized language treatment in which they will learn semantically- or phonologically based strategies to facilitate word finding difficulties, sentence formulation difficulties, or challenges in their narration and discourse. The level at which the treatment will be administered will depend on the participants' level of performance determined by the results of the language and cognitive testing done at baseline. Treatment will be administered twice a week for 10 weeks.

干预措施: individualized speech-language training (Behavioral)

control group

Active Comparator

control group will undergo standard speech-language intervention

干预措施: standard language intervention (Behavioral)

结局指标

主要结局

Mean change from baseline scores on the naming task

时间窗: through study completion, an average of 1 year

Mean change from baseline scores on the Boston Naming Test: Min score = 0; Max = 60; higher scores indicate better outcome

Mean change from baseline scores in aphasia severity

时间窗: through study completion, an average of 1 year

Mean change from baseline scores on the Western Aphasia Battery: Min score = 0; Max = 100; higher scores indicate better outcome

Mean change from baseline scores on the language probe task before and after each session

时间窗: through study completion, an average of 1 year

change on on the probe task from before the session; Min =0; Max = 100%; higher scores indicate better outcome

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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