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.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 220 (estimated) |
| Sponsor | Emory University Academic / other |
| Locations | 1 site (Atlanta, Georgia) |
| Status | Recruiting |
| Started | March 25, 2025 |
| Main results expected | February 2029 |
| Study ends | March 2029 |
| Registry record updated | April 29, 2026 |
| Trial ID | NCT06655402 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
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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.
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Deep phenotyping to explore recovery in young adults after stroke
This project will test whether a detailed health and sample-collection approach (deep phenotyping) is practical and acceptable for people aged 18–55 who have had a stroke.
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Stem cell therapy for chronic stroke recovery
This study is testing whether using a patient's own stem cells can help people with long-term stroke recovery feel better and improve their daily functioning.
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AI-based tools to help diagnose, treat and predict stroke outcomes across multiple hospitals
This study tests AI-powered tools on real-world stroke patients to see if they can improve pre-hospital triage, diagnosis, and outcome prediction while data stay securely within each hospital.
-
Web-based therapy using action observation and mirror therapy for arm weakness after stroke
This trial tests whether a mobile telerehabilitation app delivering action observation therapy (AOT) alone or combined AOT with mirror therapy (AOT-MT) can improve upper limb function in people with subacute stroke.
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Remote Ischaemic Conditioning for Fatigue After Stroke 2
Aat least 12 weeks after stroke, adults with post-stroke fatigue will try a simple hand-arm cuff treatment at home to see if it helps reduce fatigue.
-
Dual-task balance training plus computer-based cognitive training after stroke
In adults who recently had a stroke, the study tests whether adding computerized cognitive exercises to balance training improves balance and other recovery outcomes.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.