Behavioral Activation for Post-Stroke Sedentary Behavior Using Telehealth

Part of paid clinical trials in Minneapolis, Minnesota.

Sponsor
University of Minnesota
Study ID
NCT05029284
Status
Completed

Conditions

  • Stroke
  • Stroke Hemorrhagic
  • Stroke, Ischemic

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • teleABLE — BEHAVIORAL
    Participants will be guided to self-monitor their daily activities, schedule personally meaningful non-sedentary activities, collaboratively problem solve to overcome barriers to the activity, and self-assess their progress. Participants may be asked to self-monitor their activity levels and complete planned activities between sessions.

Study Details

Adults with stroke-related disability spend more time sedentary than adults without stroke-related disability, which places them at risk for poor cardiovascular health outcomes. Few interventions are designed to reduce post-stroke sedentary time. The purpose of this research is to test whether the teleABLE (Activating Behavior for Lasting Engagement) Intervention is feasible and acceptable to adults within the first 12 months post-stroke. The hypothesis is that teleABLE can be feasibly delivered using videoconferencing within the first 12 months post-stroke. 10 participants will complete assessments and activity monitoring (activPAL micro3) at 0 (baseline) and 8 (post-intervention)-weeks. Participants will complete 12 sessions of the teleABLE intervention. Findings from this study will be used to guide the intervention protocol in the planned next phase of this research.

Key Dates

Start date
Dec 20, 2021
Status verified
Jun 2025
Primary completion
Mar 18, 2024
Completion
Mar 18, 2024

Study Design

Enrollment
11 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: teleABLE
    Participants will complete 12 teleABLE sessions via videoconferencing, guided by an intervention therapist and participant workbook.

Primary Outcome Measure

Incidence of Treatment-Emergent Adverse Events [ Time Frame: week 2 through week 7 ]

Locations (1)

FacilityCityStateZIPSite coordinators
University of MinnesotaMinneapolisMinnesota55455-

Find similar trials in Minneapolis, MN

By condition
Stroke
By specialty
NeurologyBrain disorders
By research site
University of Minnesota· Minneapolis, MN

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