Clinical trial Recruiting at 1 site Interventional Ages 18 and up

A program to help stroke survivors and their caregivers through telehealth

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

Run by Emory University · NCT06655402 · Data updated 2026-11-12

This study is testing a new online program to see if it can help stroke survivors and their caregivers improve daily activities and quality of life through virtual support.

More Stroke trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment220 (estimated)
SponsorEmory University
Academic / other
Locations1 site (Atlanta, Georgia)
StatusRecruiting
StartedMarch 25, 2025
Main results expectedFebruary 2029
Study endsMarch 2029
Registry record updatedApril 29, 2026
Trial IDNCT06655402 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include stroke survivors aged 18 or older, living at home with a primary caregiver, and experiencing minimal to moderate upper extremity deficits.

Probably not a fit

Patients with significant cognitive deficits or those who do not have a caregiver living in the home may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial evaluates a novel web-based intervention called CARE-CITE, which integrates care partners into the rehabilitation process for stroke survivors. The study uses a fully virtual, two-group randomized design to compare the efficacy of CARE-CITE against an attention control group. It aims to assess improvements in upper extremity functional capacity, daily activity performance, and social participation for stroke survivors, while also evaluating the impact on care partner strain and quality of life. Participants will be recruited from the Emory Healthcare system and will engage in virtual sessions over a 29-week period.

Why it matters

Potential benefit: If successful, this program could enhance recovery outcomes for stroke survivors and reduce caregiver burden.

How similar studies have gone: Other studies have shown promise in integrating caregiver support into rehabilitation, making this approach both relevant and potentially impactful.

Who can join: the full rules

Show full inclusion / exclusion 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

Where it's running

  • Emory Rehabilitation Hospital
    Atlanta, Georgia, United States
    Recruiting

Study contacts

  • Principal investigator: Sarah Blanton, PT, DPT — Emory University
  • Study coordinator: Sarah R Blanton, PT, DPT
  • Email: sblanto@emory.edu
  • Phone: (404) 712-2222

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.