Integrated PRocess and StrategieS Training: I-PRESS Training (I-PRESS)
Primary Purpose
Acquired Brain Injury
Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
GMT combined with WMU Training
Sponsored by
About this trial
This is an interventional basic science trial for Acquired Brain Injury focused on measuring Traumatic Brain Injury, Stroke, executive dysfunction
Eligibility Criteria
Inclusion Criteria:
- Only those able to give informed consent and able to comply with the training protocol will be included.
- ≥ 6 months post-ABI at time of recruitment (expression of interest to participate either verbally or in writing)
- Adults over the age of 18.
- English language fluency (speaking)
- a combination of self/relative/friend/carer reports of everyday organisation/memory problems
Exclusion Criteria:
- Individuals with contra-indications to MRI (e.g. heart pacemaker)
- Comorbid progressive neurological disorder or neurodegenerative condition (e.g. dementia)
- Major psychiatric disorder considered likely to prevent engagement in the intervention programme (pre-ABI history of mood disorder or stable antidepressant medication will not lead to exclusion)
- History of major substance abuse problems likely to prevent engagement in the intervention programme
- Unable to give informed consent
- Unable to cooperate with the study protocol (e.g. severe impairment of hearing, vision or language)
Sites / Locations
- Lead Communirty Brain Injury Team NHS Lanarkshire Law House Airdrie RoadRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Adaptive Training (AT)
Non Adaptive Training (NA)
Arm Description
For AT participants, difficulty of the training tasks is progressively increased in response to task performance.
For NA participants, task difficulty is fixed at a relatively low level across all sessions.
Outcomes
Primary Outcome Measures
Feasibility of recruitment process.
Number of people referred from NHS eligible for screening and those entering the intervention. This will be continuously monitored throughout the study period.
Participants' drop-out rates
Number of people completing the intervention to assess drop-out rates. This will be continuously monitored throughout the study period.
Participants' coherence and adherence to the intervention.
Number of sessions attended and homework completion. This will be continuously monitored throughout the study period.
Participant evaluation of the intervention using a study-specific questionnaire.
This is a study-specific questionnaire including 8 Likert-scale items.
Secondary Outcome Measures
Changes in visuospatial working memory using the visuospatial Matrix Updating Task.
Proportion of correct responses at 0, 4 and 7 update trials.
Changes in spatial working memory using the spatial n-back task.
Proportion of correct responses at 0, 2 and 3 back trials.
Changes in visual episodic memory using the Object-location association task.
Proportion of correct responses at 6 and 8 associate trials.
Changes in fMRI data
Changes in task-related brain activity.
Changes in shifting attention using the Intra-Extra dimensional set shift test variant from CANTAB connect research web-testing.
Number of trials for which the outcome was an incorrect response (subject pressed the incorrect button within the response window), calculated across all assessed trials.
Changes in spatial planning and problem solving using the Stockings of Cambridge test variant from CANTAB connect research web-testing.
Number of assessed problems that the participant successfully completed in the minimum possible number of moves. Calculated over all assessed trials.
Changes in spatial working memory using the Spatial Working Memory test variant from CANTAB connect research web-testing.
The number of times the subject incorrectly revisits a box in which a token has previously been found. Calculated across all assessed four, six and eight token trials.
Changes in visuospatial working memory using the Spatial Span forward test variant from CANTAB connect research web-testing.
The longest sequence of boxes successfully recalled by the participant.
Changes in visuospatial working memory using the Spatial Span reverse test variant from CANTAB connect research web-testing.
The longest sequence of boxes successfully recalled by the participant.
Full Information
NCT ID
NCT04882215
First Posted
April 26, 2021
Last Updated
May 19, 2021
Sponsor
NHS Greater Glasgow and Clyde
Collaborators
University of Glasgow
1. Study Identification
Unique Protocol Identification Number
NCT04882215
Brief Title
Integrated PRocess and StrategieS Training: I-PRESS Training
Acronym
I-PRESS
Official Title
Development and Evaluation of a Novel Treatment Intervention for People With Acquired Brain Injury
Study Type
Interventional
2. Study Status
Record Verification Date
May 2021
Overall Recruitment Status
Unknown status
Study Start Date
May 18, 2021 (Actual)
Primary Completion Date
October 30, 2021 (Anticipated)
Study Completion Date
December 30, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NHS Greater Glasgow and Clyde
Collaborators
University of Glasgow
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
There is a pressing need to develop more effective interventions to remediate cognitive deficits in highly prevalent disabling conditions such as stroke, head injury and other forms of acquired brain injury (ABI). Neuropsychological rehabilitation interventions developed in a clinical setting have shown some beneficial effects, but the effectiveness of clinical interventions have potential to be enhanced if informed by findings from cognitive neuroscience. Research into cognitive training using methods such as functional magnetic resonance imaging (fMRI) has contributed to an understanding of factors that promote changes in brain function, but this approach seldom includes individuals with brain damage or cognitive deficits. Its potential for application with clinical populations is therefore uncertain, meaning that people who may benefit do not have access to interventions that may improve their health and wellbeing.
The proposed research brings together methods from neuropsychological rehabilitation and cognitive neuroscience to investigate 1) the feasibility of, and effect sizes arising from, combining an existing clinical intervention targeting mental strategies with an adaptive training programme targeting core cognitive processes, and 2) whether the novel treatment combination promotes changes in brain function that are detectable using fMRI.
This project will develop and evaluate a training intervention that aims to improve outcomes from a strategy-based rehabilitation intervention, Goal Management Training (GMT), by adding process-based cognitive training with adaptive difficulty to enhance the executive function of working memory updating (WMU). People with ABI (n=32) will complete 9 sessions of GMT, a recommended treatment for deficits in frontal-lobe executive functions, with the addition of 8 WMU training sessions with or without adaptive training. Measures of feasibility, acceptability, and fidelity will be taken, and effect sizes of differences in pre- to post-training changes on neural, cognitive, and functional measurements will be determined by comparing two experimental groups in which difficulty of the WMU training tasks either adaptively increases in response to performance or is fixed.
Detailed Description
Globally, stroke and head injury are leading causes of disability. Deficits in cognitive functions are common in these conditions, including impairment in frontal-lobe 'executive' functions such as working memory and the ability to solve problems, plan, and regulate actions in order to achieve intended goals. These deficits affect individuals' ability to live independently, work, and maintain social relationships. We propose that improving outcomes for people with acquired brain injury (ABI) requires an interdisciplinary approach in which neuropsychological rehabilitation and cognitive neuroscience complement one another.
In neuropsychological rehabilitation, interventions are classified as 'restorative' (restoration of underlying core cognitive processes including executive functions) or 'compensatory' (compensation of function through the use of external aids or learned strategies). Clinical guidelines recommend the use of 'meta-cognitive strategy training' for the treatment of deficits in frontal-lobe executive functions. Goal Management Training (GMT) is one such validated meta-cognitive strategy. GMT trains compensatory mental strategies to manage attention during multi-step tasks. GMT has been evaluated behaviourally in randomised controlled trials with positive, albeit modest, outcomes in individuals with ABI.
In cognitive neuroscience, an emerging research area concerns experience-induced neural changes referred to as neural plasticity. These may involve neural changes in: 1) task-based functional activation patterns, i.e. activity increases, decreases, or reorganisation, 2) brain structure, i.e., grey matter and white matter volume changes and 3) functional connectivity, i.e. changes in connectivity between brain regions that are recruited for a mental procedure as well as changes in the strength and magnitude.
Neuroimaging studies have demonstrated that programmes to train core cognitive processes including working memory (WM) executive functions can drive changes both in behavioural and neural measures. Performance gains after process-based training have been observed by several authors employing different training tasks and including both younger and older populations. In addition, generalisation to broad cognitive abilities such as reasoning, episodic memory, after process-based training, has been observed in both young and older adults although this area is under debate. This work has primarily involved healthy adults and whether the same findings apply to those with ABI needs to be investigated.
This research study aims to develop and evaluate a novel treatment intervention for people with ABI that combines a process-based cognitive training with a strategy-based GMT rehabilitation intervention, and to acquire functional magnetic resonance imaging (fMRI) data before and after the intervention to measure patterns of brain activity associated with a task requiring executive functions. We propose that outcomes from GMT might be improved by an adaptive, process-based intervention aimed at enhancing working memory processes. Adaptive task difficulty involves dynamic adjustment of training task demands so that the individual remains within an optimal range of performance.
i. Aims
The primary aim of the study is to investigate whether it is feasible and acceptable to deliver a novel intervention combining GMT with WMU training, within a randomised controlled trial (RCT) context in a sample of ABI individuals. A further aim is to examine the behavioural and neural changes related to the novel intervention as well as the effect sizes.
ii. Research Question
This project will combine methods from neuropsychological rehabilitation and cognitive neuroscience to answer the following: 1) Is it feasible to combine an existing treatment for executive dysfunction, GMT, with an adaptive WMU training and how much benefit is gained? 2) Does the novel treatment combination promote neural plasticity that is detectable using fMRI?
iii. Outcomes
Primary outcomes will be measures of feasibility, acceptability, and fidelity.
Secondary outcomes will be pre- to post-training change in behavioural data (i.e., neuro-psychological assessment battery, measures of cognitive task performance and everyday functioning) and fMRI data (i.e., task-related brain activity), analysed by training condition. In addition, exploratory analyses of individual differences in responsiveness to WMU training will be performed, by calculating correlations between amount of adaptive training task improvement and pre- to post-training change on neural, cognitive, and functional measurements.
iv. Design
Randomised controlled trial methodology; specifically stratified randomisation in conjunction with permuted block random allocation, using an active control group will compare two conditions: (1) GMT combined with adaptive training [AT]; (2) GMT combined with non-adaptive [NA] training. Thirty-two adults with non-progressive ABI sustained in adulthood will be recruited from the NHS.. Participants will complete a combination of standard GMT (9 sessions) and 8 WMU (AT or NA) training sessions, delivered in small groups. Neuropsychological and functional assessments will be performed before and after the intervention. In addition, fMRI scanning sessions will be conducted pre- and post-training
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acquired Brain Injury
Keywords
Traumatic Brain Injury, Stroke, executive dysfunction
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
32 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Adaptive Training (AT)
Arm Type
Experimental
Arm Description
For AT participants, difficulty of the training tasks is progressively increased in response to task performance.
Arm Title
Non Adaptive Training (NA)
Arm Type
Active Comparator
Arm Description
For NA participants, task difficulty is fixed at a relatively low level across all sessions.
Intervention Type
Behavioral
Intervention Name(s)
GMT combined with WMU Training
Intervention Description
GMT teaches the use of mental strategies to support sustained attention during complex (multi-step) task performance following an interactive programme. GMT is structured into nine modules, with interactive discussions and homework assignments. It will be conducted on a group basis.
WMU training consists of computerised working memory updating tasks in which trial accuracy and response time are recorded. Two tasks will be trained: 1. a visuo-spatial Matrix Updating (MU) and 2. a verbal Keep Track (KT). For both training tasks, level of difficulty can be modulated by increasing or decreasing the update level, i.e., the number of updates on each trial.
Primary Outcome Measure Information:
Title
Feasibility of recruitment process.
Description
Number of people referred from NHS eligible for screening and those entering the intervention. This will be continuously monitored throughout the study period.
Time Frame
From baseline to 12 weeks.
Title
Participants' drop-out rates
Description
Number of people completing the intervention to assess drop-out rates. This will be continuously monitored throughout the study period.
Time Frame
From baseline to 12 weeks.
Title
Participants' coherence and adherence to the intervention.
Description
Number of sessions attended and homework completion. This will be continuously monitored throughout the study period.
Time Frame
From baseline to 12 weeks.
Title
Participant evaluation of the intervention using a study-specific questionnaire.
Description
This is a study-specific questionnaire including 8 Likert-scale items.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Changes in visuospatial working memory using the visuospatial Matrix Updating Task.
Description
Proportion of correct responses at 0, 4 and 7 update trials.
Time Frame
Baseline and 12 weeks
Title
Changes in spatial working memory using the spatial n-back task.
Description
Proportion of correct responses at 0, 2 and 3 back trials.
Time Frame
Baseline and 12 weeks
Title
Changes in visual episodic memory using the Object-location association task.
Description
Proportion of correct responses at 6 and 8 associate trials.
Time Frame
Baseline and 12 weeks
Title
Changes in fMRI data
Description
Changes in task-related brain activity.
Time Frame
Baseline and 12 weeks
Title
Changes in shifting attention using the Intra-Extra dimensional set shift test variant from CANTAB connect research web-testing.
Description
Number of trials for which the outcome was an incorrect response (subject pressed the incorrect button within the response window), calculated across all assessed trials.
Time Frame
Baseline and 12 weeks
Title
Changes in spatial planning and problem solving using the Stockings of Cambridge test variant from CANTAB connect research web-testing.
Description
Number of assessed problems that the participant successfully completed in the minimum possible number of moves. Calculated over all assessed trials.
Time Frame
Baseline and 12 weeks
Title
Changes in spatial working memory using the Spatial Working Memory test variant from CANTAB connect research web-testing.
Description
The number of times the subject incorrectly revisits a box in which a token has previously been found. Calculated across all assessed four, six and eight token trials.
Time Frame
Baseline and 12 weeks
Title
Changes in visuospatial working memory using the Spatial Span forward test variant from CANTAB connect research web-testing.
Description
The longest sequence of boxes successfully recalled by the participant.
Time Frame
Baseline and 12 weeks
Title
Changes in visuospatial working memory using the Spatial Span reverse test variant from CANTAB connect research web-testing.
Description
The longest sequence of boxes successfully recalled by the participant.
Time Frame
Baseline and 12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Only those able to give informed consent and able to comply with the training protocol will be included.
≥ 6 months post-ABI at time of recruitment (expression of interest to participate either verbally or in writing)
Adults over the age of 18.
English language fluency (speaking)
a combination of self/relative/friend/carer reports of everyday organisation/memory problems
Exclusion Criteria:
Individuals with contra-indications to MRI (e.g. heart pacemaker)
Comorbid progressive neurological disorder or neurodegenerative condition (e.g. dementia)
Major psychiatric disorder considered likely to prevent engagement in the intervention programme (pre-ABI history of mood disorder or stable antidepressant medication will not lead to exclusion)
History of major substance abuse problems likely to prevent engagement in the intervention programme
Unable to give informed consent
Unable to cooperate with the study protocol (e.g. severe impairment of hearing, vision or language)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Katerina Pappa, BSc, MSc
Phone
01414516863
Email
a.pappa.1@research.gla.ac.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Jonathan Evans, PhD, DClin
Phone
01412113978
Email
jonathan.evans@glasgow.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jonathan Evans, PhD, DClin
Organizational Affiliation
University of Glasgow
Official's Role
Principal Investigator
Facility Information:
Facility Name
Lead Communirty Brain Injury Team NHS Lanarkshire Law House Airdrie Road
City
Carluke
State/Province
Lanarkshire
ZIP/Postal Code
ML8 5EP
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jane Moir, DClin Psy
Email
jane.moir@lanarkshire.scot.nhs.uk
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
21440699
Citation
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Results Reference
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Citation
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