RECRUITING

Emotional Recovery Post-Stroke

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StrokeMental Health Wellness 1Rehabilitation StudiesStroke Recovery

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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 purpose of this study is to evaluate whether adding an emotional wellness component to occupational therapy (OT) and/or speech therapy (ST) telerehabilitation improves overall emotional well-being and activity participation for people with stroke.

Official Title

Centering Emotional Recovery Post-Stroke

Quick Facts

Study Start:2025-05-01
Study Completion:2027-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06782321

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:21 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Self-reported stroke-related deficits in emotional wellness such as anxiety, sleep disturbance, dread, fear, loss of hope, sadness.
  2. * Have experienced ischemic or hemorrhagic stroke at least 30 days prior
  3. * Stroke-related aphasia and/or upper extremity hemiparesis
  4. * Aged 21 years or older
  5. * English as primary language
  6. * Have corrected vision to be able to read text on a screen
  7. * Able to participate fully in the study's tele-rehabilitation (Aim 1) and/or virtual group programing (Aim 2) with personally owned device (i.e., phone, tablet, or laptop) and personal Wi-Fi connection or cellular service
  8. * Cognitive, language, and motor capacity to participate fully in the study's assessment session as per the judgment of the licensed, experienced stroke tele-rehabilitation occupational or speech therapist
  1. * Unable to follow 1-2 step instructions given by the study team member during the informed consent procedures.
  2. * Pain that interferes with ability to participate in the study's upper extremity movement tasks.
  3. * Have impaired decision making capacity as determined by the U-ARE protocol for assessing capacity to provide informed consent.

Contacts and Locations

Study Contact

Kelly Rishe
CONTACT
843-985-1810
callahk@musc.edu

Principal Investigator

Michelle Woodbury, PhD
PRINCIPAL_INVESTIGATOR
Medical University of South Carolina
Lisa McTeague, PhD
PRINCIPAL_INVESTIGATOR
Medical University of South Carolina
Deena Blackett, PhD
PRINCIPAL_INVESTIGATOR
University of Central Florida

Study Locations (Sites)

Medical University of South Carolina
Charleston, South Carolina, 29425
United States

Collaborators and Investigators

Sponsor: Medical University of South Carolina

  • Michelle Woodbury, PhD, PRINCIPAL_INVESTIGATOR, Medical University of South Carolina
  • Lisa McTeague, PhD, PRINCIPAL_INVESTIGATOR, Medical University of South Carolina
  • Deena Blackett, PhD, PRINCIPAL_INVESTIGATOR, University of Central Florida

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 Date2025-05-01
Study Completion Date2027-12

Study Record Updates

Study Start Date2025-05-01
Study Completion Date2027-12

Terms related to this study

Keywords Provided by Researchers

  • Rehabilitation Studies
  • Stroke
  • Stroke Recovery

Additional Relevant MeSH Terms

  • Stroke
  • Mental Health Wellness 1