Actively Recruiting
Improving Participation After Stroke Self-Management-Rehabilitation
Led by University of Missouri-Columbia · Updated on 2026-04-28
100
Participants Needed
1
Research Sites
260 weeks
Total Duration
On this page
Sponsors
U
University of Missouri-Columbia
Lead Sponsor
U
University of Washington
Collaborating Sponsor
AI-Summary
What this Trial Is About
The overall goal of this proposed study is to evaluate the efficacy of a small-group, stroke-specific, self-management program delivered via telehealth to improve self-efficacy, activity performance, and quality of life in individuals with sub-acute stroke.
CONDITIONS
Official Title
Improving Participation After Stroke Self-Management-Rehabilitation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Less than 6 months post-stroke
- Age between 45 and 85 years
- Completed inpatient rehabilitation services if recommended
- Living in the community with or without caregiver support (not in a skilled nursing facility)
- Ability to read, write, and speak English
- Diagnosis of mild or moderate stroke (National Institutes of Health stroke score less than 16)
- Able to use videoconferencing independently or with caregiver support
You will not qualify if you...
- Severe depressive symptoms indicated by a score of 21 or higher on the Patient Health Questionnaire
- Dementia symptoms indicated by a score below 23 on the Montreal Cognitive Assessment
- Additional neurological diagnoses such as brain malignancy or previous severe stroke
- Moderate or severe aphasia indicated by an aphasia score of 2 or higher on the National Institutes of Health Stroke Scale
- Inability to provide informed consent
- Any other condition that the principal investigator determines would make participation unsafe
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Missouri
Columbia, Missouri, United States, 65211
Actively Recruiting
Research Team
A
Anna E Boone, PhD, OTR/L
CONTACT
J
Juliana H. Earwood, OTD, OTR/L
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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