RECRUITING

Efficacy and Sustainability of a Carepartner-Integrated Telerehabilitation Program for Persons With Stroke

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

Stroke is a leading cause of long-term disability. Research has placed little emphasis on integrating care partners (CP) (family members) into the rehabilitation process without increasing negative care partner outcomes. The research team has developed and implemented a novel, web-based care partner-focused intervention (CARE-CITE) designed to foster problem-solving and skill building while facilitating care partner engagement during stroke survivor (SS) upper extremity practice of daily activities in the home setting. By providing a family-focused approach to rehabilitation interventions, this project will help develop more effective treatments that improve CP and outcomes after stroke.

Official Title

Efficacy and Sustainability of a Carepartner-Integrated Telerehabilitation Program for Persons With Stroke

Quick Facts

Study Start:2025-03-25
Study Completion:2029-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06655402

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:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Must be at least18 years old,
  2. * Able to read and write English,
  3. * Mini-mental test score greater than 24
  4. * Individuals who are a spouse/partner or family member dwelling in the same household and self-identify as the primary caregiver of the SS.
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Sarah R Blanton, PT, DPT
CONTACT
(404) 712-2222
sblanto@emory.edu

Principal Investigator

Sarah Blanton, PT, DPT
PRINCIPAL_INVESTIGATOR
Emory University

Study Locations (Sites)

Emory Rehabilitation Hospital
Atlanta, Georgia, 30322
United States

Collaborators and Investigators

Sponsor: Emory University

  • Sarah Blanton, PT, DPT, PRINCIPAL_INVESTIGATOR, Emory University

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 Date2025-03-25
Study Completion Date2029-03

Study Record Updates

Study Start Date2025-03-25
Study Completion Date2029-03

Terms related to this study

Keywords Provided by Researchers

  • Stroke Survivors
  • Carepartners
  • Caregivers
  • Post-Stroke Recovery
  • Telehealth
  • Rehabilitation

Additional Relevant MeSH Terms

  • Stroke
  • Caregiver Burden