Efficacy and Sustainability of a Carepartner-Integrated Telerehabilitation Program for Persons With Stroke
Emory University · with Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) · NCT06655402
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 220
- US sites recruiting
- 1
- Study start
- March 25, 2025
- Record last updated
- April 29, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: CARE-CITE; Attention Control Group; Actigraph GT3X+
Conditions: Stroke; Caregiver Burden
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
CarePartners (CP):
Inclusion Criteria
- Must be at least18 years old,
- Able to read and write English,
- Mini-mental test score greater than 24
- Individuals who are a spouse/partner or family member dwelling in the same household and self-identify as the primary caregiver of the SS.
Stroke Survivors (SS):
Inclusion Criteria
- Must be at least18 years old
- More than 3 months and less than 2yrs post-ischemic or hemorrhagic event
- Discharged home from the hospital with minimal to moderate UE deficits (can actively initiate 20 degrees of wrist and 10 degrees of finger extension)
- Mini-mental test greater than 24
- No physician determined medical problems that would limit participation,
- Must have CP living in the home
Exclusion Criteria for CP and SS
- Significant cognitive deficits
Recruiting US locations
Emory Rehabilitation Hospital
Atlanta, GA 30322
Study contacts (from the official record)
- Sarah R Blanton, PT, DPT · (404) 712-2222 · sblanto@emory.edu
Similar studies in Georgia
All neurology studies in Georgia →- RecruitingHealthy volunteersPhase 1/Phase 2
Digital STEADI Efficacy
Friendi.fi Corporation
- Location
- Atlanta, GA
- Eligibility basics
- Ages 50+
- RecruitingHealthy volunteersPhase 1
A Study of LY4006895 in Healthy Participants With Early Symptomatic Alzheimer's Disease (AD)
Eli Lilly and Company
- Location
- Atlanta, GA + 5 other US sites
- Eligibility basics
- Ages 45–85
- RecruitingPhase 3
Study to Evaluate Safety, Efficacy and Pharmacokinetics (PK) of a Modified Regimen of Ublituximab
TG Therapeutics, Inc.
- Location
- Atlanta, GA + 35 other US sites
- Eligibility basics
- Ages 18–65
- Recruiting
Thrombectomy Using Pulsed Aspiration for Reperfusion of Brain Occlusions
RapidPulse, Inc
- Location
- Atlanta, GA + 12 other US sites
- Eligibility basics
- Ages 18–85