NCT06679803
Feasibility of a First-Line Physical Activity Intervention After Stroke
Enrolling by Invitation
NAAges 18+InterventionalTreatmentUniversity of MinnesotaInvestigator-initiated
~25 participants
Updated 2026-02-12 on ClinicalTrials.gov
What's tested:Physical Activity Chats after Stroke (PA-ChatS)
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Adherence to PA-ChatS sessions
Measured over 6-weeks
+1 more outcome measured
Conditions
Where it's being run
1 sites across 1 statesMinnesota1
Study leadership
- Emily Kringle, PhD, OTR/L · PRINCIPAL_INVESTIGATOR · University of Minnesota
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
Stroke diagnosis confirmed by imaging
Admitted to Fairview Health System (Minnesota) at the time of study enrollment or discharged to a community-based setting from Fairview Health System within 3 months before study enrollment
Able and willing to participate fully in the study and provide informed consent or proxy consent with participant assent
Exclusion
Discharge anticipated to a transitional care unit, skilled nursing facility, or other non-community-based care setting
Severe cognitive or communication impairments (inability to respond accurately to complete study screening questions or to provide informed consent or assent
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 psychiatric condition and/or alcohol or substance abuse within the past 12 months
Current diagnosis of a terimnal illness and/or receiving hospice care
History of allergic reaction to adhesives that precludes the use of an adhesive necessary for adherence to activPAL measurement
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 metropolitan area
Investigator discretion for safety or adherence reasons
What this trial measures
- Adherence to PA-ChatS sessions6-weeks
Percentage of participants who complete 6 out of 6 (100%) of PA-ChatS sessions. Session completion will be documented by the study intervention therapist and total count of sessions completed will be computed after the last intervention session is delivered.
- Adherence to wearable activity tracker6-weeks
Percentage of participants who use the wearable activity tracker (Fitbit Inspire 3) an average of 5 of 7 days/week during the 6-week intervention period. Data will be exported from Fitbit to compute average number of days per week the Fitbit was used.