Spaced Retrieval as Treatment for Aphasia
Primary Purpose
Aphasia, Acquired, Aphasia Primary Progressive
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Spaced Retrieval Practice
Sponsored by
About this trial
This is an interventional treatment trial for Aphasia, Acquired focused on measuring Adaptive Spaced-Retrieval, Aphasia, Anomia, Anki
Eligibility Criteria
Inclusion Criteria:
- presence of a post-stroke word finding deficit (i.e. aphasia), or primary progressive aphasia.
- ability to evaluate the correctness of one's own responses when subsequently provided the with the correct answer
Exclusion Criteria:
- diagnosis of a neurological disorder other than post-stroke or primary progressive aphasia
- inability to evaluate the correctness of ones responses when subsequently provided with the correct answer
Sites / Locations
- Baycrest Health Sciences
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Spaced Repetition
Arm Description
Two weeks (10 sessions) of online picture-naming training with 60 words.
Outcomes
Primary Outcome Measures
Change in Picture Naming performance across conditions
Word retention assessed after treatment
Secondary Outcome Measures
Full Information
NCT ID
NCT04623125
First Posted
October 29, 2020
Last Updated
March 27, 2023
Sponsor
Rotman Research Institute at Baycrest
Collaborators
Heart and Stroke Foundation of Canada
1. Study Identification
Unique Protocol Identification Number
NCT04623125
Brief Title
Spaced Retrieval as Treatment for Aphasia
Official Title
Spaced Retrieval as Treatment for Aphasia: Does Adaptive Spacing Enhance Picture Naming Performance?
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
October 1, 2020 (Actual)
Primary Completion Date
January 1, 2022 (Actual)
Study Completion Date
January 1, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rotman Research Institute at Baycrest
Collaborators
Heart and Stroke Foundation of Canada
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Spaced Repetition training has been found to be more effective than massed repetition for individuals with aphasia. This study seeks to examine the relative efficiency of three kinds of spacing for picture-naming training: traditional random presentation, non-adaptive spaced repetition, and adaptive spaced repetition.
Detailed Description
Participants undergo a screening evaluation including the Quick Aphasia Battery (administered via teleconferencing software), and a preliminary picture naming test of approximately 300 pictures, used to select individual items for treatment. Participants then undertake online picture naming training for 30 minutes a day, over two weeks. Pictures are repeated according to three different schedules to be compared: random presentation, non-adaptive spaced repetition, and adaptive spaced repetition. We compare the number of pictures successfully learned and the verbal reaction time for the pictures assigned to the three conditions.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aphasia, Acquired, Aphasia Primary Progressive
Keywords
Adaptive Spaced-Retrieval, Aphasia, Anomia, Anki
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
21 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Spaced Repetition
Arm Type
Experimental
Arm Description
Two weeks (10 sessions) of online picture-naming training with 60 words.
Intervention Type
Behavioral
Intervention Name(s)
Spaced Retrieval Practice
Intervention Description
Online picture-naming training with 60 words which the participant experiences word-retrieval difficulties. Cards are shuffled arranged by the computerized training program.
Primary Outcome Measure Information:
Title
Change in Picture Naming performance across conditions
Description
Word retention assessed after treatment
Time Frame
Change from baseline to post-intervention immediately after two weeks of daily sessions, and one month followup.
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
presence of a post-stroke word finding deficit (i.e. aphasia), or primary progressive aphasia.
ability to evaluate the correctness of one's own responses when subsequently provided the with the correct answer
Exclusion Criteria:
diagnosis of a neurological disorder other than post-stroke or primary progressive aphasia
inability to evaluate the correctness of ones responses when subsequently provided with the correct answer
Facility Information:
Facility Name
Baycrest Health Sciences
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M6A 2E1
Country
Canada
12. IPD Sharing Statement
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Spaced Retrieval as Treatment for Aphasia
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