NCT07649135Recruiting
Feasibility of a Remotely Delivered Step Count Intervention in Chronic Stroke
Feasibility of Engaging Stroke Survivors in a Brief Step Count Intervention During Chronic Stroke
Source: ClinicalTrials.gov · Last updated 10 Jul 2026
Brief summary (registry, in English)
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).
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 24 (estimated)
- First submitted
- 9 Jun 2026
- Start date
- 8 Jul 2026
- Primary completion date
- 30 Nov 2026
- Lead sponsor
- University of Minnesota
- Diseases
- Stroke
- NCT number
- NCT07649135
What you commit to
- Study type: Interventional
- Planned participants: 24
- From 8 Jul 2026 to the primary completion date, 30 Nov 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- 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)
- 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
- Concurrent participation in another rehabilitation intervention research study
Other illness
- 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
- History of allergic reaction to adhesives that precludes the use of an adhesive necessary for adherence to activPAL measurement
Other
- Severe cognitive or communication impairments (inability to respond accurately to complete study screening questions or to provide informed consent or assent)
- Uses wheelchair as primary mobility aid outside of home setting
- Inability to speak, read, or understand English
- Resides more than 50 miles outside of the Twin Cities, Minnesota metropolitan area
- Investigator discretion for safety or adherence reasons
Who the study is looking for
- 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
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of Minnesota Coordinator of this site? Confirm its status | Minneapolis | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.