- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04604444
Changes in Neuroplasticity Following Intensive Rehabilitation of Aphasia and/or Apraxia of Speech
October 30, 2024 updated by: Ellika Schalling, Karolinska Institutet
Evaluating the Effects of Intensive Speech and Language Rehabilitation Regarding Neuroplasticity, Speech, Language, Communication Skills and Quality of Life for People With Acquired Aphasia and/or Apraxia of Speech in the Chronic Phase
The present study aims to investigate the short- and long-term effects of two weeks of intensive speech-language pathology intervention with additional physiotherapy, on aphasia and apraxia of speech (AOS) and their neural correlates in thirty persons with chronic stroke.
Changes are studied following intensive treatment of aphasia and AOS with standardised speech-language testing and testing of communication and with voxel-based morphometry (VBM) analysis and resting state functional connectivity (rsFC).
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
This study explores structural and functional brain changes in relation to effects on speech, language, communication and quality of life following an intensive speech-language program with additional physiotherapy for persons with chronic aphasia and/or apraxia of speech.
The participants are consecutively recruited from a rehabilitation centre providing intensive treatment for chronic conditions following stroke or other neurological injuries.
The speech-language pathologists (SLPs) involved in the rehabilitation programs perform the testing directly before and after intensive intervention with an additional follow up after 16 weeks (+-2) with testing of speech-language, communication and quality of life.
The SLPs have more than five years of experience of working with aphasia and are specialised in working with intensive treatment, they have acquired in-depth knowledge on how to evaluate and treat aphasia and apraxia of speech in lectures and workshops.
The test procedure is recorded with camcorder and voice recorder to provide the opportunity to access data retrospectively and to minimize bias by including an external SLP who makes a second blinded evaluation on randomized participants' performance in ASRS, BNT and CAT by studying the video and voice material.
Structural and functional neuroplasticity is also investigated with voxel-based morphometry (VBM) analysis, resting state functional connectivity (rsFC) in domain-specific (language processing) and domain-general (executive and attention processing).
This intensive neuro-rehabilitation program for speech and language deficits named Multimodal Intensive Rehabilitation for Aphasia and Apraxia of Speech (MIRAA) is defined as an ICAP (Intensive Comprehensive Aphasia Program) with focus on both speech and language function and communicative activity and participation.
The program is intensive: consisting of ten days of training (5 hours/day), with a minimum of three hours dedicated to speech and language rehabilitation with additional physical therapy.
The program includes both individual treatment, group therapy and computer-based therapy.
The therapy is individually set up after the participant's goals together with the team including SLPs, physiotherapists and a board-certified neurologist and/or specialist in rehabilitation medicine.
The goals are set by the participants, family members and clinicians the first day of the program.
The participant and their significant other are offered education with the aim to enhance the knowledge on communication, the key concepts of neuroplasticity and other functions and strategies important in everyday life.
The treatment methods being used are evidence-based and/or widely used multimodal programs covering the need for extensive training programs targeting both impairment-based therapy and functional communication.
The specific questions are: Does ten days of with an intensive comprehensive aphasia/AOS program result in any clinical significant improvements in speech and/or language function and other cognitive skills for participants with chronic aphasia and/or apraxia of speech?
Does the intensive intervention have any effect on the quality of everyday life concerning speech and language functions, activity and communicative participation for people with chronic aphasia and apraxia of speech?
Can functional and anatomical brain changes be detected following ten days of intensive speech and language intervention for these participants?
Study Type
Interventional
Enrollment (Estimated)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Marika J Schütz, Ph.D student
- Phone Number: 0046737570430
- Email: marika.schutz@uu.se
Study Locations
-
-
-
Uppsala, Sweden, 141 86
- Recruiting
- Uppsala Universitet
-
Contact:
- Marika Schütz, Ph.D student
- Phone Number: 0046737570430
- Email: marika.schutz@uu.se
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Aphasia 7 months post stroke diagnosed by SLP
- Apraxia of Speech 7 months post stroke diagnosed by SLP
Exclusion Criteria:
- Dementia
- Severe loss of sight
- Severe loss of hearing
- Metal implants (preventing fMRI)
- Claustrophobia (preventing fMRI)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Multimodal Intensive Rehabilitation of Aphasia/AOS (MIRAA)
A minimum of 3 hour speech-language training daily during 10 days.
|
Intensive Comprehensive Aphasia (ICAP) and Apraxia of Speech Program
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Comprehensive Aphasia Test (CAT) language battery, in pilot Swedish test A-ning.
Time Frame: Changes from baseline in language battery scores at 2 and 18 weeks.
|
Comprehension of spoken language: minimum score 0, maximum score 66; Comprehension of written langugage: minimum score 0, maximum score 62; Repetition: minimum score 0, maximum score 74; Naming: minimum score 0, maximum score no limit; Reading: minimum score 0, maximum score 70; Writing: minimum score 0, maximum score 76.
Higher scores mean better outcome in language functions.
|
Changes from baseline in language battery scores at 2 and 18 weeks.
|
|
Rating scale for apraxia of speech (SkaFTA, Swedish version of ASRS)
Time Frame: Changes from baseline scores at 2 and 18 weeks.
|
Minimum score 0, maximum score 52.
Lower scores mean better outcome in speech functions.
|
Changes from baseline scores at 2 and 18 weeks.
|
|
Communication Outcome After Stroke (COAST)
Time Frame: Changes from baseline scores at 2 and 18 weeks.
|
Minimum score 0, maximum score 100.
Higher scores mean better outcome in communication.
|
Changes from baseline scores at 2 and 18 weeks.
|
|
Goal Attainment Scaling (GAS), International Classification of Functioning, Disability and Health (ICF). Aphasia adapted GAS scales for self-evaluation of communication functions, participation and activity.
Time Frame: Changes from baseline at week 18.
|
Minimum score -2, maximum score +2.
Higher scores mean better outcome in quality of life.
|
Changes from baseline at week 18.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Barrow Neurological Institute Screening for Higher Cerebral Function (BNIS)
Time Frame: Changes from baseline at week 2
|
Minimum score 0, maximum score 50.
Higher scores mean better outcome in cognition.
|
Changes from baseline at week 2
|
|
Boston Naming Test (BNT)
Time Frame: Changes from baseline at week 2 and week 18.
|
Minimum score 0, maximum score 60.
Higher scores mean better outcome in naming ability.
|
Changes from baseline at week 2 and week 18.
|
|
Protocol for Apraxia of Speech (TAX)
Time Frame: Changes from baseline at week 2 and week 18.
|
Minimum score 0, maximum score 30.
Lower scores mean mean better outcome in speech functions and non verbal oral apraxia.
|
Changes from baseline at week 2 and week 18.
|
|
Comprehensive Aphasia Test (CAT), subtest cognitive screening
Time Frame: Changes from baseline in Comprehensive Aphasia Test cognitive screening scores at 2 and 18 weeks.
|
Minimum score 0, maximum score 38.
Higher scores mean better outcome in cognitive functions.
|
Changes from baseline in Comprehensive Aphasia Test cognitive screening scores at 2 and 18 weeks.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Ellika Schalling, Professor, Uppsala University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 2, 2017
Primary Completion (Estimated)
December 31, 2026
Study Completion (Estimated)
December 31, 2027
Study Registration Dates
First Submitted
September 11, 2020
First Submitted That Met QC Criteria
October 23, 2020
First Posted (Actual)
October 27, 2020
Study Record Updates
Last Update Posted (Actual)
October 31, 2024
Last Update Submitted That Met QC Criteria
October 30, 2024
Last Verified
October 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2016/1651-31
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
All individual patient data (IPD) that underlie results in a publication.
IPD Sharing Time Frame
2020-2030
IPD Sharing Access Criteria
Swedish National Data Service open source http://snd.gu.se/sv/dashboard/data-description/0a1f0ee0-454e-4d66-b43f-b235bfe821a6#publications
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ICF
- ANALYTIC_CODE
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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