Improving Participation After Stroke Self-Management-Rehabilitation

Description

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

Stroke

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Study Overview

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Study Details

Study overview

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.

Efficacy of the Improving Participation After Stroke Self-Management-Rehabilitation (IPASS-R) Program in Sub-acute Stroke

Improving Participation After Stroke Self-Management-Rehabilitation

Condition
Stroke
Intervention / Treatment

-

Contacts and Locations

Columbia

University of Missouri, Columbia, Missouri, United States, 65211

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * 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)
  • * ability to read, write, and speak English
  • * diagnosis of mild or moderate stroke (National Institutes of Health stroke score \<16)
  • * able to use videoconferencing independently or with caregiver support
  • * 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
  • * inability to provide informed consent
  • * any other condition not otherwise specified that the PI determines would render participation in this study as unsafe for the participant

Ages Eligible for Study

45 Years to 85 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Missouri-Columbia,

Anna E Boone, PhD, OTR/L, PRINCIPAL_INVESTIGATOR, University of Missouri Occupational Therapy

Study Record Dates

2029-12-15