No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
24 (estimated)
Sponsor
University of Minnesota · Other
Who this trial is looking for
This trial is looking for people who have had a stroke at least 6 months ago. Participants will join 6 sessions over 6 weeks with an occupational therapist and track their steps.
Are You a Good Fit for This Trial?
Rules you outParkinson's diseaseAlzheimer's diseaseMultiple sclerosisDementiaCancer
You may be able to join if
I have been diagnosed with a stroke confirmed by imaging.
I had my stroke 6 or more months ago.
I am considered inactive based on a specific activity questionnaire.
I have a support person I see in person at least once a week.
I can participate fully in the study and provide consent.
You may not be able to join if
I am currently receiving care in a nursing home or similar facility.
I am receiving outpatient rehabilitation services like physical therapy.
I have severe cognitive or communication problems.
I am currently pregnant or expect to be pregnant in the next 8 weeks.
I have another serious neurological condition like Parkinson's or dementia.
I have cancer and am receiving chemotherapy or radiation.
I was treated for a psychiatric condition or substance abuse in the last year.
I cannot speak, read, or understand English.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
The goal of this study is to explore the feasibility of a new approach to rehabilitation that focuses on step count. Participants will complete 6 telephone or Zoom-based sessions with an occupational therapist over 6 weeks and use a step count tracker during that time. They will also complete questionnaires, assessments, surveys, and physical activity measurements during study weeks 0 (baseline), …
The goal of this study is to explore the feasibility of a new approach to rehabilitation that focuses on step count. Participants will complete 6 telephone or Zoom-based sessions with an occupational therapist over 6 weeks and use a step count tracker during that time. They will also complete questionnaires, assessments, surveys, and physical activity measurements during study weeks 0 (baseline), 3 (mid-point), 7 (post-intervention) and 12 (follow-up).
Trial Locations
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Facility
City
State
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Status
Eligibility Criteria
Inclusion Criteria:
* Stroke diagnosis confirmed by imaging
* Stroke occurred 6 or more months before study enrollment
* Meet criteria for "inactive" on the International Physical Activity Questionnaire-Short Form
* Able to identify a support person that they interact with in-person at least once p…
Inclusion Criteria:
* Stroke diagnosis confirmed by imaging
* Stroke occurred 6 or more months before study enrollment
* Meet criteria for "inactive" on the International Physical Activity Questionnaire-Short Form
* Able to identify a support person that they interact with in-person at least once per week
* Able and willing to participate fully in the study and provide informed consent or proxy consent with participant assent
Exclusion Criteria:
* Currently receiving care in a transitional care unit, skilled nursing facility, or other institutional care setting
* Currently receiving outpatient neurorehabilitation services (e.g., physical therapy, occupational therapy, speech therapy)
* Severe cognitive or communication impairments (inability to respond accurately to complete study screening questions or to provide informed consent or assent)
* Currently pregnant or expecting to become pregnant in the next 8 weeks Comorbid neurological disorder (Parkinson's disease, multiple sclerosis, amyotrophic lateral sclerosis, myasthenia gravis, dementia, Alzheimer's disease, Huntington's disease, glioblastoma, spinal cord injury, cerebral palsy)
* Comorbid cancer, currently undergoing chemotherapy or radiation treatment
* Received inpatient treatment or was hospitalized for a psychiatric condition and/or alcohol or substance abuse within the past 12 months
* Current diagnosis of a terminal illness and/or currently receiving hospice care
* History of allergic reaction to adhesives that precludes the use of an adhesive necessary for adherence to activPAL measurement
* Uses wheelchair as primary mobility aid outside of home setting
* Inability to speak, read, or understand English
* Concurrent participation in another rehabilitation intervention research study
* Resides more than 50 miles outside of the Twin Cities, Minnesota metropolitan area
* Investigator discretion for safety or adherence reasons
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