RECRUITING

Improving Participation After Stroke Self-Management-Rehabilitation

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Conditions

StrokeSelf-ManagementTelehealthActivities of daily livingCommunity engagement

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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.

Official Title

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

Quick Facts

Study Start:2024-12-16
Study Completion:2029-12-15
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06588647

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.

Ages Eligible for Study:45 Years to 85 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * less than 6 months post-stroke
  2. * age 45-85 years
  3. * completed inpatient rehabilitation services (if recommended)
  4. * living in the community with or without caregiver support (i.e., not living in a skilled nursing facility)
  5. * ability to read, write, and speak English
  6. * diagnosis of mild or moderate stroke (National Institutes of Health stroke score \<16)
  7. * able to use videoconferencing independently or with caregiver support
  1. * severe depressive symptoms as indicated by a score ≥21 on the Patient Health Questionnaire
  2. * dementia symptoms as indicated by a score of \<23 on the Montreal Cognitive Assessment
  3. * additional neurological diagnoses (e.g., brain malignancy, previous severe stroke)
  4. * (4) moderate or severe aphasia as indicated by a National Institutes of Health Stroke Scale aphasia score of ≥ 2
  5. * inability to provide informed consent
  6. * any other condition not otherwise specified that the PI determines would render participation in this study as unsafe for the participant

Contacts and Locations

Study Contact

Anna E Boone, PhD, OTR/L
CONTACT
5738827023
booneae@umsystem.edu
Juliana H. Earwood, OTD, OTR/L
CONTACT
5738846681
jmhudson@health.missouri.edu

Principal Investigator

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

Study Locations (Sites)

University of Missouri
Columbia, Missouri, 65211
United States

Collaborators and Investigators

Sponsor: University of Missouri-Columbia

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

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-12-16
Study Completion Date2029-12-15

Study Record Updates

Study Start Date2024-12-16
Study Completion Date2029-12-15

Terms related to this study

Keywords Provided by Researchers

  • Stroke
  • Self-Management
  • Telehealth
  • Activities of daily living
  • Community engagement

Additional Relevant MeSH Terms

  • Stroke