Improving Participation After Stroke Self-Management-Rehabilitation
ConditionStroke
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age45-85
SponsorUniversity of Missouri-Columbia
About this trial
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.
Eligibility criteria
Qualifiers
less than 6 months post-stroke
age 45-85 years
completed inpatient rehabilitation services (if recommended)
living in the community with or without caregiver support (i.e., not living in a skilled nursing facility)
Disqualifiers
severe depressive symptoms as indicated by a score ≥21 on the Patient Health Questionnaire
dementia symptoms as indicated by a score of <23 on the Montreal Cognitive Assessment
additional neurological diagnoses (e.g., brain malignancy, previous severe stroke)
(4) moderate or severe aphasia as indicated by a National Institutes of Health Stroke Scale aphasia score of ≥ 2
Trial design
Treatments tested in this trial
- Improving Participation after Stroke Self-Management Program (IPASS)
- Chronic Disease Self-Management Program (CDSMP)
Treatment groups
100 Participants
are divided into 2 treatment groupsSponsors and collaborators
University of Missouri-Columbia
Lead sponsor
University of Washington
Collaborator
National Institutes of Health (NIH)
Collaborator
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborator
University of Illinois at Chicago
Collaborator
Source ClinicalTrials.gov