Status:

COMPLETED

duoABLE for People With Stroke and Their Caregivers

Lead Sponsor:

University of Minnesota

Collaborating Sponsors:

American Occupational Therapy Foundation

Conditions:

Stroke

Stroke Ischemic

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The goal of this intervention study is to test whether a behavioral program that involves people with stroke and their caregivers is acceptable, safe, and can promote physically active lifestyles usin...

Eligibility Criteria

Inclusion

  • Inclusion Criteria (Stroke Participants):
  • Stroke diagnosed more than 6 months ago
  • Are 18 years of age or older
  • Report ≥6 hours of sedentary behavior on a typical day OR report engagement in ≤90 minutes of moderate-to-vigorous physical activity in the past week
  • Reside in a community-based setting
  • Are mobile within their home, with or without an assistive device and without physical assistance
  • Are able to identify an eligible caregiver who will engage in assessments and intervention.
  • Inclusion Criteria (Caregiver Participants):
  • Are 18 years of age or older
  • Report ≥6 hours of sedentary behavior on a typical day OR report engagement in ≤90 minutes of moderate-to-vigorous physical activity in the past week
  • Reside in a community-based setting
  • Are mobile within their home, with or without an assistive device and without physical assistance
  • Exclusion Criteria (Stroke Participants):
  • Severe aphasia
  • Are currently receiving chemotherapy or radiation treatments for cancer
  • Have a medical diagnosis of neurodegenerative disorder (i.e., dementia, Parkinson's disease, multiple sclerosis, amyotrophic lateral sclerosis, glioblastoma)
  • Received inpatient treatment for substance use disorder or psychiatric condition within the past 12 months
  • Have a history of skin sensitivity related to adhesives
  • Are pregnant or expecting to become pregnant in the next 2 months
  • Reside in an institutional setting
  • Are currently incarcerated
  • Exclusion Criteria (Caregiver Participants):
  • Have a history of skin sensitivity related to adhesives
  • Are currently receiving chemotherapy or radiation treatments for cancer
  • Have a medical diagnosis of neurodegenerative disorder (i.e., dementia, Parkinson's disease, multiple sclerosis, amyotrophic lateral sclerosis, glioblastoma)
  • Received inpatient treatment for substance use disorder or psychiatric condition within the past 12 months
  • Are pregnant or expecting to become pregnant in the next 2 months
  • Reside in an institutional setting
  • Are currently incarcerated

Exclusion

    Key Trial Info

    Start Date :

    September 1 2023

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    August 24 2024

    Estimated Enrollment :

    16 Patients enrolled

    Trial Details

    Trial ID

    NCT05964400

    Start Date

    September 1 2023

    End Date

    August 24 2024

    Last Update

    October 21 2024

    Active Locations (1)

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    1

    School of Kinesiology, University of Minnesota

    Minneapolis, Minnesota, United States, 55455