About this trial
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.
Eligibility criteria
Qualifiers
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
Disqualifiers
We will exclude individuals with unstable major psychiatric conditions or neurodegenerative conditions.
Trial design
Treatments tested in this trial
- Occupational Performance Coaching (OPC)
- computer cognitive training program (CogniFit)
Treatment groups
Sponsors and collaborators
Queen's University
Lead sponsor
Providence Care Hospital
Collaborator
Bruyère Health Research Institute.
Collaborator