- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04042779
Development of a Model-based Working Memory Training and Investigation of Its Comparative Efficacy (sMarT)
June 30, 2020 updated by: University Hospital, Basel, Switzerland
Development of a Model-based Working Memory Training and Investigation of Its Comparative Efficacy: A Randomized, Double-blind Study on Healthy Adults
This study is to investigate the efficacy of model-based Working Memory (WM) training using an appropriate control condition.
The interventions are a model-based, a single-task and a multiple-task training on WM in order to compare the efficacies of these different training approaches for WM.
A sham intervention acts as active control group.
Each intervention will be presented on a tablet device.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
131
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 Locations
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Basel, Switzerland, 4031
- Department of Neurology, University Hospital Basel
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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
50 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Informed consent as documented by signature
Exclusion Criteria:
- Medical history of neurological or psychiatric disorders
- Any history of substance abuse
- Color vision deficiency
- Inability to used table devices
- Montreal Cognitive Assessment < 26
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: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: model-based WM training
In order to build the model-based WM training, existing tasks used to assess the different component of the Baddeley's model will be reviewed on their findings according to test-retest reliability and construct validity.
For each component - phonological loop, visuospatial sketchpad, episodic buffer and central executive - the task with the highest reliability and validity will be chosen and then build the basis for the computerized training program.
This procedure results in a model-based, adaptive, computerized training program for WM.
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model-based WM training program: four sessions a week, 45 minutes each; lasting for three weeks
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Active Comparator: single-task WM training
The basis for the single-task training administered to the second group will be the widely used "dual-n-back training paradigm" suggested by Jaeggi et al. (2008).
A complex dual n-back task including a visual and an auditory WM task will be implemented for tablet devices.
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single-task WM training program: four sessions a week, 45 minutes each; lasting for three weeks
|
|
Active Comparator: multiple-task WM training
Verbal WM tasks - particularly letter span and digit span tasks - and a visuospatial WM task are most commonly used (e.g.
Dahlin et al., 2008; Klingberg et al., 2005; Westerberg et al., 2007).
Therefore, a multiple-task training including these tasks will be administered to the third group.
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multiple-task WM training program: four sessions a week, 45 minutes each; lasting for three weeks
|
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Sham Comparator: sham intervention
Active control group that as well performs a training, however not based on WM.
To exclude the involvement of WM, a motor training will be administered to the control group.
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motor training program: four sessions a week, 45 minutes each; lasting for three weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Rotation Span Task Score
Time Frame: assessment at baseline (=T2) and 3 weeks after baseline (=T3)
|
First, the distractor task is judging whether a rotated letter is presented correctly, or is a mirrored image of the letter.
Second, the to-be-remembered items are arrows of either short or long length and pointing in one of eight different directions.
Finally, the rotation-arrow sequence is repeated from two to five times per trial.
Scores are calculated by summing the number of arrows correctly recalled in the correct order.
|
assessment at baseline (=T2) and 3 weeks after baseline (=T3)
|
|
Change in Symmetry Span Task Score
Time Frame: assessment at baseline (=T2) and 3 weeks after baseline (=T3)
|
First, the distractor task is judging whether a displayed shape is symmetrical along its vertical axis.
Second, the to-be-remembered items are locations of red squares in a 4×4 grid of potential locations.
Finally, the number of symmetry-location pairs varied from two to five times per trial.
Scores are calculated by summing the number of red square locations correctly recalled in the correct order.
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assessment at baseline (=T2) and 3 weeks after baseline (=T3)
|
|
Change in Operation Span Task Score
Time Frame: assessment at baseline (=T2) and 3 weeks after baseline (=T3)
|
Subjects first solve a math problem, and then see a letter, and then solve another math problem, and see another letter.
This math-letter sequence is repeated from three to seven times for each trial with an unpredictable length each time.
After each math-letter sequence, subjects are asked to recall, in order, the preceding letters.
Scores are calculated by summing the number of letters correctly recalled in the correct order.
|
assessment at baseline (=T2) and 3 weeks after baseline (=T3)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Rotation Span Task Score
Time Frame: assessment at baseline (=T2) and 12 weeks after baseline (=T4)
|
First, the distractor task is judging whether a rotated letter is presented correctly, or is a mirrored image of the letter.
Second, the to-be-remembered items are arrows of either short or long length and pointing in one of eight different directions.
Finally, the rotation-arrow sequence is repeated from two to five times per trial.
Scores are calculated by summing the number of arrows correctly recalled in the correct order.
|
assessment at baseline (=T2) and 12 weeks after baseline (=T4)
|
|
Change in Symmetry Span Task Score
Time Frame: assessment at baseline (=T2) and 12 weeks after baseline (=T4)
|
First, the distractor task is judging whether a displayed shape is symmetrical along its vertical axis.
Second, the to-be-remembered items are locations of red squares in a 4×4 grid of potential locations.
Finally, the number of symmetry-location pairs varied from two to five times per trial.
Scores are calculated by summing the number of red square locations correctly recalled in the correct order.
|
assessment at baseline (=T2) and 12 weeks after baseline (=T4)
|
|
Change in Operation Span Task Score
Time Frame: assessment at baseline (=T2) and 12 weeks after baseline (=T4)
|
Subjects first solve a math problem, and then see a letter, and then solve another math problem, and see another letter.
This math-letter sequence is repeated from three to seven times for each trial with an unpredictable length each time.
After each math-letter sequence, subjects are asked to recall, in order, the preceding letters.
Scores are calculated by summing the number of letters correctly recalled in the correct order.
|
assessment at baseline (=T2) and 12 weeks after baseline (=T4)
|
|
Change in Trail making Test A/B
Time Frame: assessment at baseline (=T2) and 3 weeks after baseline (=T3) and 12 weeks after baseline (=T4)
|
The Trail making Test A/B consists of two parts in which the subject is instructed to connect a set of 25 dots as quickly as possible while still maintaining accuracy with the time taken to complete the test being used as the primary performance metric
|
assessment at baseline (=T2) and 3 weeks after baseline (=T3) and 12 weeks after baseline (=T4)
|
|
Change in Rey Auditory Verbal Learning test
Time Frame: assessment at baseline (=T2) and 3 weeks after baseline (=T3) and 12 weeks after baseline (=T4)
|
Participants are read a list of 15 words aloud by the person administering the test.
The entire test takes 10-15 minutes to administer and includes five presentations of a 15 word list (list A), followed by a free recall of a second word list (list B).
Finally there is a sixth recall trial of the first list (List A).
Recognition is tested by asking which of 30 words wre read aloud from list A and which were not.
The words are read at a rate of one word per second.
The overall goal of the task is to repeat all of the words the participant can remember in any order.
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assessment at baseline (=T2) and 3 weeks after baseline (=T3) and 12 weeks after baseline (=T4)
|
|
Change in Rey Osterrieth Complex Figure Test
Time Frame: assessment at baseline (=T2) and 3 weeks after baseline (=T3) and 12 weeks after baseline (=T
|
The Rey-Osterrieth complex figure test (ROCF) is a neuropsychological assessment in which examinees are asked to reproduce a complicated line drawing, first by copying it freehand (recognition), and then drawing from memory (recall).
Each copy is scored for the accurate reproduction and placement of 18 specific design elements.
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assessment at baseline (=T2) and 3 weeks after baseline (=T3) and 12 weeks after baseline (=T
|
|
Change in Raven's Progressive Matrices
Time Frame: assessment at baseline (=T2) and 3 weeks after baseline (=T3) and 12 weeks after baseline (=T
|
The Raven's Progressive Matrices is administered as a nonverbal group test.
It is typically a 60-item test used in measuring abstract reasoning and regarded as a non-verbal estimate of fluid intelligence.
Many patterns are presented in the form of a 6×6, 4×4, 3×3, or 2×2 matrix, giving the test its name.
All of the questions on the Raven's progressives consist of visual geometric design with a missing piece.
The test taker is given six to eight choices to pick from before filling in the missing piece.
Scoring on the Raven's Progressive Matrices is based on two factors: How many out of 60 matrices problems the tester correctly solved and the age of the tester.
For each age group, N number of correct answers corresponds to a certain percentile score.
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assessment at baseline (=T2) and 3 weeks after baseline (=T3) and 12 weeks after baseline (=T
|
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Change in Depression Anxiety Stress Scales
Time Frame: assessment at baseline (=T2) and 3 weeks after baseline (=T3) and 12 weeks after baseline (=T
|
The Depression Anxiety Stress Scales is made up of 42 self-report items to be completed over five to ten minutes, each reflecting a negative emotional symptom.
Each of these is rated on a four-point Likert scale of frequency or severity of the participants' experiences over the last week with the intention of emphasising states over traits.
These scores ranged from 0, meaning that the client believed the item "did not apply to them at all", to 3 meaning that the client considered the item to "apply to them very much, or most of the time".
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assessment at baseline (=T2) and 3 weeks after baseline (=T3) and 12 weeks after baseline (=T
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Stefano Magon, Dr. phil., Department of Neurology, University Hospital Basel
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)
July 2, 2019
Primary Completion (Actual)
March 13, 2020
Study Completion (Actual)
March 13, 2020
Study Registration Dates
First Submitted
July 31, 2019
First Submitted That Met QC Criteria
July 31, 2019
First Posted (Actual)
August 2, 2019
Study Record Updates
Last Update Posted (Actual)
July 1, 2020
Last Update Submitted That Met QC Criteria
June 30, 2020
Last Verified
June 1, 2020
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2018-01226; me19Magon
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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