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Clinical Trials/NCT04204356
NCT04204356
Completed
N/A

The Effect of Speech and Language Therapy With and Without Transcranial Direct-current Stimulation on Discourse Production in People With Post-stroke Aphasia: a Pilot Randomised Controlled Trial

King's College London1 site in 1 country6 target enrollmentNovember 25, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Aphasia
Sponsor
King's College London
Enrollment
6
Locations
1
Primary Endpoint
Verb token total
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Aphasia is a language impairment caused by brain injury such as stroke that affects the ability to understand and express language, read and write due to damage in the language regions of the brain. Non-invasive brain stimulation (NIBS) techniques like transcranial direct-current stimulation (tDCS) have been found to improve aphasia treatment effects in post stroke patient populations such as improved naming abilities.

However, the effect of tDCS on more functional, higher level language skills such as discourse production (i.e. story telling, giving instructions) has yet to be understood.Therefore the aim of this study is to determine the potential effectiveness of tDCS as an adjunct to speech and language therapy (SLT) to improve discourse speech production in people with post-stroke aphasia. It is hypothesised that SLT combined with tDCS will result in greater improvements in discourse language production compared to SLT on its own.

Registry
clinicaltrials.gov
Start Date
November 25, 2019
End Date
November 5, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • aphasia caused by a single stroke
  • at least 6 months post stroke
  • at least 18 years old
  • competent English speaker prior to stroke
  • right handed prior to stroke
  • normal aided or unaided visual acuity
  • willing to participate and to comply with the proposed block of intervention and testing regime.

Exclusion Criteria

  • Persons with
  • neurological symptoms or history of a neurological event other than their stroke
  • contraindications to tDCS including history of epilepsy or seizures and pacemakers
  • global/severe aphasia
  • cognitive impairment identified by a score less than 20/30 in the Montreal Cognitive Assessment
  • left-handed dominance prior to stroke
  • visual problems which interfere with persons' ability to access visual materials (i.e. pictures)
  • inability to attend sessions

Outcomes

Primary Outcomes

Verb token total

Time Frame: 30 minutes

The number of all verb occurrences in a language sample

Verb type total

Time Frame: 30 minutes

The number of distinct verbs in a sample

Secondary Outcomes

  • Total number of utterances(30 minutes)
  • Communicative Effectiveness Index (CETI)(10 minutes)
  • Total number of words(30 minutes)
  • Hospital Anxiety and Depression Scale (HADS)(10 minutes)
  • Montreal Cognitive Assessment (MoCA)(15 minutes)
  • Aphasia Impact Questionnaire-21 (AIQ)(15 minutes)
  • Predicate argument structure (PAS)(30 minutes)

Study Sites (1)

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