StrokeNo acronymsNCT07759791
Supporting Re-engagement in Life: Coaching to Enhance Participation in Valued Activities Following Stroke
A study testing Occupational Performance Coaching (OPC) and computer cognitive training program (CogniFit) in people with Stroke, run by Queen's University at 2 sites in Canada.
Trial summary
The goal of this clinical trial is to determine whether Occupational Performance Coaching (OPC), a person-centered, strength-based intervention, can improve participation in valued activities among adults who have experienced a stroke and recently completed community- or clinic-based stroke rehabilitation. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Stroke
- What is being tested?
- Occupational Performance Coaching (OPC) and computer cognitive training program (CogniFit)
- Type of treatment
- Medical device, Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 118 participants
- Where
- 2 sitesCanada
- Study dates
- 10 Nov 2025to 30 Jun 2028
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Be living in the community (home, retirement home)
- Have completed publicly funded rehabilitation
- Are 3 to 12 months post-first stroke.
- Be able to communicate in English
- Have adequate comprehension and memory to participate in the coaching process. (Must have FIM scores of at least 3 (needs assistance less than 50% of the time) for comprehension and memory at the time of discharge from inpatient rehabilitation).
Who cannot join
- We will exclude individuals with unstable major psychiatric conditions or neurodegenerative conditions.
Trial locations and contacts
2 sites in 1 country. Contact the study team or a site near you to ask about taking part.
Canada2 sites, 2 recruiting
- Recruiting
Providence care Hospital
Kingston, Ontario
Esther Chang, 613-533-3170, keslab@queensu.ca
Benjamin Ritsma
- Not yet recruiting
Bruyere Health
Ottawa, Ontario, K1N 5C8
Dorothy Kessler, 6135336551, dk75@queensu.ca
Hhillel Finestone
About this study
The goal of this clinical trial is to determine whether Occupational Performance Coaching (OPC), a person-centered, strength-based intervention, can improve participation in valued activities among adults who have experienced a stroke and recently completed community- or clinic-based stroke rehabilitation.
The main questions it aims to answer are:
Read more
Does OPC improve performance and satisfaction with participation in personally valued activities?
Does OPC improve participation self-efficacy, physical activity, cognition, and emotional well-being compared to an active attention control intervention?
Researchers will compare the OPC group to an active attention control group to see if OPC leads to greater improvements in participation and secondary outcomes.
Participants will:
Be randomized to receive either OPC (delivered virtually, including collaborative goal-setting and problem-solving) or an active attention control intervention.
Complete assessments of participation in valued activties, physical activity (using movement sensors), self-efficacy, cognition, and mood immediately after treatment and at 3 months.
A subset of 20 participants from intervention group will take part in interviews to share their experiences.
Read the detailed description
Most stroke survivors, access of all levels of impairment, have difficulty returning to valued activities and social roles, leading to loss of sense of self and purpose in life and impacting both physical and mental health. Occupational Performance Coaching (OPC) shows promise in quickly returning people to their valued activities, thereby offering hope and improving well-being. This project asks, "Will OPC, an innovative adaptive approach to returning people quickly to their valued activities, lead to increased participation for individuals with stroke?"
The experience of stroke is devastating for both stroke survivors and their families. The process of picking up the pieces, adjusting, and finding ways to engage in activities that provide meaning and purpose is complex, requiring emotional and practical support, access to information, and opportunities to test abilities and try new ways of doing. With much of the focus of rehabilitation practice and guidelines being on reducing impairment, it is not surprising that stroke survivors feel lost and ill-prepared to participate in their valued activities when formal rehabilitation ends. Effective adaptive interventions are needed to return people quickly to activities to prevent negative outcomes associated with decreased participation.
OPC is a person-centred, strengths-based, adaptive approach that focuses on providing emotional support, collaborative goal setting, solution-focused problem-solving, and experimentation to build knowledge, skills, and self-efficacy for participation. OPC capitalizes on modifiable factors influencing participation after stroke. and builds the skills needed for stroke survivors to continue setting and achieving goals on their own.
OPC is the most widely researched coaching intervention in occupational therapy and stroke rehabilitation. PI Kessler the lead international researcher testing OPC with adults with neurological conditions, namely stroke and multiple sclerosis. Pilot feasibility studies demonstrated the potential of OPC, delivered in person or virtually, to return individuals living with stroke to valued activities within 8-10 sessions.
Based on previous participation research, through enhancing participation in personally valued activities, OPC may enhance self-efficacy, physical activity, cognitive abilities, and emotional well-being.
The proposed study will establish the efficacy of OPC for improving participation in valued activities (Canadian Occupational Performance Measure), self-efficacy (Participation Strategeis Self-Efficacy Scale), physical activity (AcivPal activity monitor), cognition (CogniFit computerized assessments : a)Trail Making Test measures processing speed, shifting and visual attention; b) the Stroop test measures inhibition, updating, visual perception, naming, processing speed and response time; and c) the Visual Working Memory Span Test measures spatial perception, short-term memory, visual short-term memory, non-verbal memory, working memory, planning, processing speed, and response time), and emotional well-being (Generalized Anxiety Disorders Scale-7 and Brief Patient Health Questionnaire ). In addition, wthe investigators will conduct a process evaluation to examine characteristics of participants that act as mediators or moderators to improve participation in valued activity goals and to explore how OPC works with different subgroups of stroke participants (e.g., stroke severity, age, sex, and gender).
The investigators will conduct a double-blind randomized controlled trial to test whether OPC delivered virtually enhances participation in valued activities among people with stroke compared to an active control condition.
The investigators will recruit 118 patients from inpatient stroke rehabilitation and randomly assign them (stratified by stroke severity) to OPC (intervention group) or computerized cognitive therapy with check-ins (active control group) at the end of publicly funded rehabilitation. Participants will be 3 to 12 months post-stroke. A blinded research assistant will administer outcomes at baseline, post-intervention, and at 3-month follow-up. The primary outcome will be participation in valued activities. Secondary outcomes will be participation self-efficacy, physical activity, cognition, and emotional well-being. The investigators will examine mediators and moderators that impact the outcome of OPC and interview a subsample of 20 participants who receive OPC to better understand how OPC works with people of different stroke severity, age, sex, and gender.
Participants, blinded to study purposes, will receive 10 one-hour sessions of either OPC or an active control delivered virtually using Zoom over 15 weeks.
Between-group differences across the three timepoints for each outcome will be tested using repeated measures ANOVA. Interview transcripts will be analyzed using content analysis.
This project addresses an important knowledge gap related to improving participation among patients with stroke. The investigators will establish the efficacy of OPC, an established adaptive intervention, and expand our understanding of how it works. Without evidence-based interventions to promote participation, stroke survivors will continue to struggle to return to valued activities and miss out on associated health benefits (physical, cognitive, emotional). This work will also build on evidence for virtual approaches to stroke rehabilitation; these approaches have the potential to improve accessibility to rehabilitation for stroke survivors.
- Conditions
- Stroke
- Being tested
- Occupational Performance Coaching (OPC), computer cognitive training program (CogniFit)
- Keywords
- Stroke rehabilitation, Participation, Occupational Performance Coaching
- Medical subject headings
- Stroke
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Occupational Performance Coaching (OPC)Behavioural
Occupational Performance Coaching (OPC) is an innovative, person-centered, strengths-based intervention designed to enhance participation in valued activities after stroke. OPC targets modifiable factors such as goal setting, self-efficacy, emotional support, problem-solving, and individualized education. Through a collaborative process, therapists partner with stroke survivors to identify challenges, set meaningful goals, and experiment with tailored solutions, refining them until successful strategies are found. Research shows OPC is feasible, acceptable, and effective, with participants demonstrating significant improvements in performance, satisfaction, and re-engagement in valued activities within 8-10 sessions, both in-person and via telerehabilitation. By fostering physical, cognitive, and emotional well-being, OPC addresses barriers like social isolation, physical inactivity, and low self-efficacy. Delivered virtually, OPC overcomes challenges in accessing rehabilitation, parti
computer cognitive training program (CogniFit)Device
Active control (AC) group will receive access to the CogniFit computer-based cognitive training program, a personalized brain training tool designed to target perception, attention, memory, and reasoning.While cognitive training can improve global cognition, working memory, attention, and executive function, it has not shown effects on daily activities or depression.
| Study group | Role | What they receive |
|---|---|---|
| OPC Intervention Group (occupational performance couching groups | Experimental | Participants will receive 10 one-hour telerehabilitation sessions delivered via Zoom (Zoom Video Communications Inc., San Jose, CA) over a 15-week period. Sessions will be delivered by an Occupational Therapist trained in the Occupational Performance Coaching (OPC) approach and in telerehabilitation service delivery. The 15-week period allows flexibility for scheduling (e.g., to accommodate appointments or vacations). Receives: Behavioral: Occupational Performance Coaching (OPC) |
| Active Control (AC) Group | Active comparator | Participants will receive access to the CogniFit (computer cognitive training program (CogniFit Inc. © 2024) for 15 weeks. There will be 10 virtual contacts via Zoom. The AC interventionist will be trained in telerehabilitation service delivery. The program is designed to train perception, attention, memory, and reasoning. Receives: Device: computer cognitive training program (CogniFit) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Canadian Occupational Performance Measure (COPM)
The Canadian Occupational Performance Measure (COPM) is a reliable, valid, and responsive tool frequently used in stroke rehabilitation outcome studies. Using the COPM, participants identify problems related to participation in valued activities that are then rated by participants for performance and satisfaction with current status on a scale of 1-10, where 10 indicates optimal performance or satisfaction. Numbers are summed and divided by the number of goals.
Measured: Baseline, periprocedural, and 3-months after periprocedural assessment
Secondary outcomes (5)
Participation Strategies Self-Efficacy Scale (PS-SES)
The Participation Strategies Self-Efficacy Scale (PS-SES) is a 35-item scale that measures self-efficacy in using strategies for participation in home, community, work, and social activities. Each item is scored on a scale of 1 (not at all confident) to 10 (totally confident) total score ranges from 35 to 350 with higher scores indicating higher self-efficacy.
Measured: Baseline, periprocedural, and 3-months after periprocedural assessment
Time spent in active veruss sedentary activity
Time spent in active (i.e., standing, walking) versus sedentary (i.e., sitting, lying) activites willk be measured using the ActivPal 4 activity monitor (PAL Technologies Ltd., Glasgow, UK). The ActivPal is a small, lightweight wearable device that measures movement with a triaxial accelerometer and body posture with a gyroscope. Consistent with recommendations for obtaining a good representation of typical physical activity, it will be worn for seven consecutive days ateach data colleciton timepoint. An average of active versus sedentary time will be calculated.
Measured: Baseline, periprocedural, and 3-months after periprocedural assessment
Generalized Anxiety Disorders Scale-7 (GAD-7)
The Generalized Anxiety Disorders Scale-7 (GAD-7) is a brief 7-item screening tool for anxiety that captures the frequency of anxiety-related symptoms. The GAD-7 is a valid, reliable, and responsive measure commonly used in stroke rehabilitation research. Items are socred on a scale of 0 (not at all) to 3 (nearly everyday). Total score ranges from 0-21 with higher scores indicating higher anxiety.
Measured: Baseline, periprocedural, and 3-months after periprocedural assessment
Executive Functioning
Executive functioning will be measured using the following CogniFit computerized assessments : a) the Trail Making Test (TMT) measures processing speed, shifting and visual attention; b) the Stroop test measures inhibition, updating, visual perception, naming, processing speed and response time; and c) the Visual Working Memory Span Test measures spatial perception, short-term memory, visual short-term memory, non-verbal memory, working memory, planning, processing speed, and response time. These tests have demonstrated reliability and validity with older adults.
Overall executive functioning will be represented using Z scores.
Measured: Baseline, periprocedural, and 3-months after periprocedural assessment
Brief Patient Health Questionnaire (PhQ-9)
The Brief Patient Health Questionnaire (PHQ-9) is a brief 9-item screening tool for depression. PhQ-9 is a valid, reliable, and responsive measure commonly used in stroke rehabilitation research. Items are scored on a scale of 0 (not at all) to 3 (nearly every day). Total score ranges form 0 to 27 with higher scores indicating higher depression.
Measured: Baseline, periprocedural, and 3-months after periprocedural assessment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Aug 2026
- Study start10 Nov 2025
- Primary completion27 Nov 2027 (estimated)
- Study completion30 Jun 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for StrokeStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 118 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Queen's University
- Sponsor type
- University, hospital or other
- Collaborators
- Providence Care Hospital, Bruyère Health Research Institute.
- Responsible party
- Principal investigator, Dorothy Kessler, Queen's University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07759791
- Sponsor's protocol ID
- G-25-0040433
- Other IDs
- G-24-0036389
- Acronym
- No acronyms
- Status last verified
- Nov 2025
- First submitted
- 31 Jul 2026
- Last updated
- 12 Aug 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Anonymized data will be deopsited in the Queen's University research data repository
Study at a glance
From the registry record, last updated by the sponsor on 12 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Supporting Re-engagement in Life: Coaching to Enhance Participation in Valued Activities Following Stroke
- ClinicalTrials.gov ID
- NCT07759791
- Acronym / sponsor ID
- No acronyms / G-25-0040433
- Conditions
- Stroke
- Keywords
- Stroke rehabilitation, Participation, Occupational Performance Coaching
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 118 participants (estimated)
- Lead sponsor
- Queen's UniversityUniversity, hospital or other
- Collaborators
- Providence Care Hospital, Bruyère Health Research Institute.
- Study start
- 10 Nov 2025 (actual)
- Primary completion
- 27 Nov 2027 (estimated)
- Study completion
- 30 Jun 2028 (estimated)
- First posted
- 12 Aug 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this clinical trial is to determine whether Occupational Performance Coaching (OPC), a person-centered, strength-based intervention, can improve participation in valued activities among adults who have experienced a stroke and recently completed community- or clinic-based stroke rehabilitation.
The main questions it aims to answer are:
Does OPC improve performance and satisfaction with participation in personally valued activities?
Does OPC improve participation self-efficacy, physical activity, cognition, and emotional well-being compared to an active attention control intervention?
Researchers will compare the OPC group to an active attention control group to see if OPC leads to greater improvements in participation and secondary outcomes.
Participants will:
Be randomized to receive either OPC (delivered virtually, including collaborative goal-setting and problem-solving) or an active attention control intervention.
Complete assessments of participation in valued activties, physical activity (using movement sensors), self-efficacy, cognition, and mood immediately after treatment and at 3 months.
A subset of 20 participants from intervention group will take part in interviews to share their experiences.
Detailed description
Most stroke survivors, access of all levels of impairment, have difficulty returning to valued activities and social roles, leading to loss of sense of self and purpose in life and impacting both physical and mental health. Occupational Performance Coaching (OPC) shows promise in quickly returning people to their valued activities, thereby offering hope and improving well-being. This project asks, "Will OPC, an innovative adaptive approach to returning people quickly to their valued activities, lead to increased participation for individuals with stroke?"
The experience of stroke is devastating for both stroke survivors and their families. The process of picking up the pieces, adjusting, and finding ways to engage in activities that provide meaning and purpose is complex, requiring emotional and practical support, access to information, and opportunities to test abilities and try new ways of doing. With much of the focus of rehabilitation practice and guidelines being on reducing impairment, it is not surprising that stroke survivors feel lost and ill-prepared to participate in their valued activities when formal rehabilitation ends. Effective adaptive interventions are needed to return people quickly to activities to prevent negative outcomes associated with decreased participation.
OPC is a person-centred, strengths-based, adaptive approach that focuses on providing emotional support, collaborative goal setting, solution-focused problem-solving, and experimentation to build knowledge, skills, and self-efficacy for participation. OPC capitalizes on modifiable factors influencing participation after stroke. and builds the skills needed for stroke survivors to continue setting and achieving goals on their own.
OPC is the most widely researched coaching intervention in occupational therapy and stroke rehabilitation. PI Kessler the lead international researcher testing OPC with adults with neurological conditions, namely stroke and multiple sclerosis. Pilot feasibility studies demonstrated the potential of OPC, delivered in person or virtually, to return individuals living with stroke to valued activities within 8-10 sessions.
Based on previous participation research, through enhancing participation in personally valued activities, OPC may enhance self-efficacy, physical activity, cognitive abilities, and emotional well-being.
The proposed study will establish the efficacy of OPC for improving participation in valued activities (Canadian Occupational Performance Measure), self-efficacy (Participation Strategeis Self-Efficacy Scale), physical activity (AcivPal activity monitor), cognition (CogniFit computerized assessments : a)Trail Making Test measures processing speed, shifting and visual attention; b) the Stroop test measures inhibition, updating, visual perception, naming, processing speed and response time; and c) the Visual Working Memory Span Test measures spatial perception, short-term memory, visual short-term memory, non-verbal memory, working memory, planning, processing speed, and response time), and emotional well-being (Generalized Anxiety Disorders Scale-7 and Brief Patient Health Questionnaire ). In addition, wthe investigators will conduct a process evaluation to examine characteristics of participants that act as mediators or moderators to improve participation in valued activity goals and to explore how OPC works with different subgroups of stroke participants (e.g., stroke severity, age, sex, and gender).
The investigators will conduct a double-blind randomized controlled trial to test whether OPC delivered virtually enhances participation in valued activities among people with stroke compared to an active control condition.
The investigators will recruit 118 patients from inpatient stroke rehabilitation and randomly assign them (stratified by stroke severity) to OPC (intervention group) or computerized cognitive therapy with check-ins (active control group) at the end of publicly funded rehabilitation. Participants will be 3 to 12 months post-stroke. A blinded research assistant will administer outcomes at baseline, post-intervention, and at 3-month follow-up. The primary outcome will be participation in valued activities. Secondary outcomes will be participation self-efficacy, physical activity, cognition, and emotional well-being. The investigators will examine mediators and moderators that impact the outcome of OPC and interview a subsample of 20 participants who receive OPC to better understand how OPC works with people of different stroke severity, age, sex, and gender.
Participants, blinded to study purposes, will receive 10 one-hour sessions of either OPC or an active control delivered virtually using Zoom over 15 weeks.
Between-group differences across the three timepoints for each outcome will be tested using repeated measures ANOVA. Interview transcripts will be analyzed using content analysis.
This project addresses an important knowledge gap related to improving participation among patients with stroke. The investigators will establish the efficacy of OPC, an established adaptive intervention, and expand our understanding of how it works. Without evidence-based interventions to promote participation, stroke survivors will continue to struggle to return to valued activities and miss out on associated health benefits (physical, cognitive, emotional). This work will also build on evidence for virtual approaches to stroke rehabilitation; these approaches have the potential to improve accessibility to rehabilitation for stroke survivors.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| OPC Intervention Group (occupational performance couching groups | Experimental | Behavioral: Occupational Performance Coaching (OPC)Participants will receive 10 one-hour telerehabilitation sessions delivered via Zoom (Zoom Video Communications Inc., San Jose, CA) over a 15-week period. Sessions will be delivered by an Occupational Therapist trained in the Occupational Performance Coaching (OPC) approach and in telerehabilitation service delivery. The 15-week period allows flexibility for scheduling (e.g., to accommodate appointments or vacations). |
| Active Control (AC) Group | Active comparator | Device: computer cognitive training program (CogniFit)Participants will receive access to the CogniFit (computer cognitive training program (CogniFit Inc. © 2024) for 15 weeks. There will be 10 virtual contacts via Zoom. The AC interventionist will be trained in telerehabilitation service delivery. The program is designed to train perception, attention, memory, and reasoning. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Be living in the community (home, retirement home)
- Have completed publicly funded rehabilitation
- Are 3 to 12 months post-first stroke.
- Be able to communicate in English
- Have adequate comprehension and memory to participate in the coaching process. (Must have FIM scores of at least 3 (needs assistance less than 50% of the time) for comprehension and memory at the time of discharge from inpatient rehabilitation).
Key exclusion criteria (1 listed)
- We will exclude individuals with unstable major psychiatric conditions or neurodegenerative conditions.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Occupational Performance Coaching (OPC)Occupational Performance Coaching (OPC) is an innovative, person-centered, strengths-based intervention designed to enhance participation in valued activities after stroke. OPC targets modifiable factors such as goal setting, self-efficacy, emotional support, problem-solving, and individualized education. Through a collaborative process, therapists partner with stroke survivors to identify challenges, set meaningful goals, and experiment with tailored solutions, refining them until successful strategies are found. Research shows OPC is feasible, acceptable, and effective, with participants demonstrating significant improvements in performance, satisfaction, and re-engagement in valued activities within 8-10 sessions, both in-person and via telerehabilitation. By fostering physical, cognitive, and emotional well-being, OPC addresses barriers like social isolation, physical inactivity, and low self-efficacy. Delivered virtually, OPC overcomes challenges in accessing rehabilitation, parti | Behavioural | OPC Intervention Group (occupational performance couching groups |
| computer cognitive training program (CogniFit)Active control (AC) group will receive access to the CogniFit computer-based cognitive training program, a personalized brain training tool designed to target perception, attention, memory, and reasoning.While cognitive training can improve global cognition, working memory, attention, and executive function, it has not shown effects on daily activities or depression. | Device | Active Control (AC) Group |
Primary outcome
Canadian Occupational Performance Measure (COPM)
Time frame: Baseline, periprocedural, and 3-months after periprocedural assessment
The Canadian Occupational Performance Measure (COPM) is a reliable, valid, and responsive tool frequently used in stroke rehabilitation outcome studies. Using the COPM, participants identify problems related to participation in valued activities that are then rated by participants for performance and satisfaction with current status on a scale of 1-10, where 10 indicates optimal performance or satisfaction. Numbers are summed and divided by the number of goals.
5 secondary outcomes
Participation Strategies Self-Efficacy Scale (PS-SES)
Time frame: Baseline, periprocedural, and 3-months after periprocedural assessment
Time spent in active veruss sedentary activity
Time frame: Baseline, periprocedural, and 3-months after periprocedural assessment
Generalized Anxiety Disorders Scale-7 (GAD-7)
Time frame: Baseline, periprocedural, and 3-months after periprocedural assessment
Executive Functioning
Time frame: Baseline, periprocedural, and 3-months after periprocedural assessment
Brief Patient Health Questionnaire (PhQ-9)
Time frame: Baseline, periprocedural, and 3-months after periprocedural assessment
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Aug 2026.
- Individual participant dataSharing planned: Yes. Anonymized data will be deopsited in the Queen's University research data repository
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Occupational Performance Coaching (OPC) and computer cognitive training program (CogniFit) in people with Stroke, run by Queen's University at 2 sites in Canada.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 12 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Dorothy Kessler, PhD (613-533-6551, dk75@queensu.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Canadian Occupational Performance Measure (COPM) (time frame: Baseline, periprocedural, and 3-months after periprocedural assessment). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Aug 2026.