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OptiCogs: A Multicomponent Intervention to Rehabilitate Cognitive Impairment in People Post-stroke

Primary Purpose

Stroke, Cardiovascular, Cognitive Impairment

Status
Completed
Phase
Not Applicable
Locations
Ireland
Study Type
Interventional
Intervention
OptiCogs Online
Sponsored by
University of Limerick
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Stroke, Cardiovascular focused on measuring Feasibility, Stroke, Cognitive impairment, Multicomponent rehabilitation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • People with a physician-confirmed diagnosis of stroke. Stroke may be ischaemic or haemorrhagic in nature.
  • People aged ≥18 years old; with confirmed mild to moderate cognitive impairment using the Oxford Cognitive Screen (OCS) (in accordance with cut-offs for impairment for OCS-plus subtasks (Demeyere et al. 2021a) and the Addenbroke's Examination III (ACE III) with a cut-off score of 88/100 (Takenoshita et al. 2019).
  • People post-stroke who have a Modified Rankin Scale (MRS) score of 0-3
  • Capacity to provide informed consent
  • People post-stroke who are able to express their basic needs, verbally or not
  • Have access to a smartphone, laptop or tablet with an internet connection
  • Willingness/ interest in participating in an online intervention
  • Physician-confirmed suitability to partake in this intervention

Exclusion Criteria:

  • Physician-confirmed contraindications for undertaking physical activity e.g., safety, presence of unstable heart disease
  • People with diagnosed TIA will be excluded
  • People post-stroke with known active delirium or dementia will be excluded
  • People post-stroke with a diagnosis of known pre-stroke cognitive impairment
  • People post-stroke with moderate or severe visuospatial neglect

Sites / Locations

  • University of Limerick

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Intervention group

Arm Description

OptiCogs Online is a 6-week telehealth intervention consisting of cognitive, physical activity and educational components. Cognitive component of the intervention: Throughout the six-week intervention period, there will be three individualised one-to-one cognitive sessions (occurring on week one, week three and week five), delivered by an occupational therapist. Physical activity: The physical activity component will be delivered via telehealth by a physiotherapist. Aerobic: Progressions from Week 1-Week 6 will result in individual achieving 60 mins moderate intensity aerobic activity @ frequency of 3 times per week as tolerated. Muscular strengthening: Progressions from Week 1-Week 6 will result in the person post-stroke achieving 10 strengthening exercises x 10 reps x 3 sets @ frequency of 3 times per week as tolerated. Cognitive education: The cognitive education component is underpinned by the Bridges stroke self-management package and based on self-efficacy principles.

Outcomes

Primary Outcome Measures

Recruitment rate
The proportion of participants who are recruited to the study.
Adherence rate
The proportion of participants who adhere to the treatment protocol of 6 weeks. We will determine the level of adherence to the intervention protocol using the self-report diary.
Adverse events
Number of participants with adverse events as a measure of safety. Adverse events include a fall, illness, medical complication etc.
Acceptability of OptiCogs Online
The proportion of participants reporting that OptiCogs Online is acceptable. Acceptability (satisfaction) of the OptiCogs intervention will be assessed using a self-report questionnaire developed by the researchers containing 5-point Likert scales: 1= "strongly disagree"; 2= "disagree"; 3= "neutral"; 4= "agree"; 5= "strongly agree".
Retention rate
The proportion of participants who are lost to follow-up

Secondary Outcome Measures

Oxford Cognitive Screen-plus (OCS-plus)
Changes in cognitive function from pre-intervention to post-intervention in accordance with the cut-offs for impairment for OCS-Plus subtasks.
Addenbrooke's Cognitive Assessment (III) ACE (III)
Changes in cognitive function from pre-intervention to post-intervention in accordance with ACE III score out of 100.
Fatigue severity scale (FSS)
). The FSS is a 9-item scale which measures the severity of fatigue and its effect on ADLs on a 7-point scale. The FSS is shown as a valid and reliable measure of fatigue in people post-stroke
PROMIS-10 Physical Functioning
• Physical function (PF) will be assessed using a physical functioning subset of the patient reported outcomes measurement information system (PROMIS) scale.
Stroke Specific Quality of Life Scale
• Mood and social participation will be assessed using the relevant subscales of the Stroke-Specific Quality of Life Scale-12 (SSQoL-12).

Full Information

First Posted
February 21, 2022
Last Updated
November 1, 2022
Sponsor
University of Limerick
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1. Study Identification

Unique Protocol Identification Number
NCT05414539
Brief Title
OptiCogs: A Multicomponent Intervention to Rehabilitate Cognitive Impairment in People Post-stroke
Official Title
A Multicomponent Intervention to Rehabilitate Cognitive Impairment in People Post-stroke: Single-arm Feasibility Study
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
May 9, 2022 (Actual)
Primary Completion Date
June 24, 2022 (Actual)
Study Completion Date
June 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Limerick

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
OptiCogs Online is a complex multicomponent intervention comprising of cognitive, physical activity and educational components.
Detailed Description
OptiCogs Online was developed in accordance with the MRC framework for the development and evaluation of complex interventions. Given the known interactions and interconnectivity of cognitive domains required for optimal cognitive functioning post-stroke, a systematic review of 64 studies addressing all types of non-pharmacological rehabilitation interventions which may improve multiple cognitive domains in people post-stroke was conducted. Within this review, rehabilitation interventions were categorised as multicomponent interventions, physical activity interventions, cognitive rehabilitation interventions, NIBS protocols, occupational-based interventions and other interventions. The most consistent evidence in our systematic review and meta-analysis supported multicomponent interventions, with significant improvement demonstrated for general cognitive function and memory outcomes. Specifically, multicomponent interventions wherein a form of cognitive rehabilitation was conducted in conjunction with a form of physical activity were shown to improve cognitive functioning in people post-stroke. As well as meta-analytic evidence, we drew from qualitative findings which explored the perspectives of PpS, caregivers and healthcare professionals on the design and delivery of an intervention to improve cognitive functioning in PpS. Qualitative findings and input from clinical experts emphasised the importance of information provision, peer support and meaningful engagement. As such, each component of OptiCogs Online is supplemented with an educational or 'cognitive education' session wherein group discussion covers different aspects of cognitive functioning. As well as drawing on findings from our qualitative study, this 'cognitive education' component is underpinned by the Bridges stroke self-management package and based on self-efficacy principles. To this end, a complex multicomponent intervention comprising of cognitive, physical activity and educational components was developed in line with the MRC framework.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Cardiovascular, Cognitive Impairment
Keywords
Feasibility, Stroke, Cognitive impairment, Multicomponent rehabilitation

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
A non-randomised single-arm feasibility study using a pre-test: post-test design.
Masking
None (Open Label)
Allocation
N/A
Enrollment
9 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention group
Arm Type
Experimental
Arm Description
OptiCogs Online is a 6-week telehealth intervention consisting of cognitive, physical activity and educational components. Cognitive component of the intervention: Throughout the six-week intervention period, there will be three individualised one-to-one cognitive sessions (occurring on week one, week three and week five), delivered by an occupational therapist. Physical activity: The physical activity component will be delivered via telehealth by a physiotherapist. Aerobic: Progressions from Week 1-Week 6 will result in individual achieving 60 mins moderate intensity aerobic activity @ frequency of 3 times per week as tolerated. Muscular strengthening: Progressions from Week 1-Week 6 will result in the person post-stroke achieving 10 strengthening exercises x 10 reps x 3 sets @ frequency of 3 times per week as tolerated. Cognitive education: The cognitive education component is underpinned by the Bridges stroke self-management package and based on self-efficacy principles.
Intervention Type
Other
Intervention Name(s)
OptiCogs Online
Intervention Description
A multicomponent intervention to rehabilitate cognitive deficits in people post-stroke
Primary Outcome Measure Information:
Title
Recruitment rate
Description
The proportion of participants who are recruited to the study.
Time Frame
6 weeks
Title
Adherence rate
Description
The proportion of participants who adhere to the treatment protocol of 6 weeks. We will determine the level of adherence to the intervention protocol using the self-report diary.
Time Frame
6 weeks
Title
Adverse events
Description
Number of participants with adverse events as a measure of safety. Adverse events include a fall, illness, medical complication etc.
Time Frame
6 weeks
Title
Acceptability of OptiCogs Online
Description
The proportion of participants reporting that OptiCogs Online is acceptable. Acceptability (satisfaction) of the OptiCogs intervention will be assessed using a self-report questionnaire developed by the researchers containing 5-point Likert scales: 1= "strongly disagree"; 2= "disagree"; 3= "neutral"; 4= "agree"; 5= "strongly agree".
Time Frame
6 weeks
Title
Retention rate
Description
The proportion of participants who are lost to follow-up
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Oxford Cognitive Screen-plus (OCS-plus)
Description
Changes in cognitive function from pre-intervention to post-intervention in accordance with the cut-offs for impairment for OCS-Plus subtasks.
Time Frame
6 weeks
Title
Addenbrooke's Cognitive Assessment (III) ACE (III)
Description
Changes in cognitive function from pre-intervention to post-intervention in accordance with ACE III score out of 100.
Time Frame
6 weeks
Title
Fatigue severity scale (FSS)
Description
). The FSS is a 9-item scale which measures the severity of fatigue and its effect on ADLs on a 7-point scale. The FSS is shown as a valid and reliable measure of fatigue in people post-stroke
Time Frame
6 weeks
Title
PROMIS-10 Physical Functioning
Description
• Physical function (PF) will be assessed using a physical functioning subset of the patient reported outcomes measurement information system (PROMIS) scale.
Time Frame
6 weeks
Title
Stroke Specific Quality of Life Scale
Description
• Mood and social participation will be assessed using the relevant subscales of the Stroke-Specific Quality of Life Scale-12 (SSQoL-12).
Time Frame
6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: People with a physician-confirmed diagnosis of stroke. Stroke may be ischaemic or haemorrhagic in nature. People aged ≥18 years old; with confirmed mild to moderate cognitive impairment using the Oxford Cognitive Screen (OCS) (in accordance with cut-offs for impairment for OCS-plus subtasks (Demeyere et al. 2021a) and the Addenbroke's Examination III (ACE III) with a cut-off score of 88/100 (Takenoshita et al. 2019). People post-stroke who have a Modified Rankin Scale (MRS) score of 0-3 Capacity to provide informed consent People post-stroke who are able to express their basic needs, verbally or not Have access to a smartphone, laptop or tablet with an internet connection Willingness/ interest in participating in an online intervention Physician-confirmed suitability to partake in this intervention Exclusion Criteria: Physician-confirmed contraindications for undertaking physical activity e.g., safety, presence of unstable heart disease People with diagnosed TIA will be excluded People post-stroke with known active delirium or dementia will be excluded People post-stroke with a diagnosis of known pre-stroke cognitive impairment People post-stroke with moderate or severe visuospatial neglect
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sara Hayes, PhD
Organizational Affiliation
University of Limerick
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Limerick
City
Limerick
Country
Ireland

12. IPD Sharing Statement

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OptiCogs: A Multicomponent Intervention to Rehabilitate Cognitive Impairment in People Post-stroke

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