Telerehabilitation coaching program for people after ischemic stroke
Official title: The Effect of Telerehabilitation-Based Coaching Interventions (TeleSCoP) on Self-Efficacy, Modifiable Risk Factors, and Repeated Hospitalizations in Patients With Ischemic Stroke
Run by Akdeniz University · NCT05940350 · Data updated 2026-11-12
This program tests whether discharge education plus a three-month telerehabilitation coaching package helps adults 45+ who had an ischemic stroke improve self-management, lower modifiable risk factors, and reduce repeat hospital visits.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 45 Years and up |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Akdeniz University Academic / other |
| Locations | 1 site (Antalya) |
| Status | Recruiting |
| Started | February 1, 2025 |
| Main results expected | December 31, 2025 |
| Study ends | March 1, 2026 |
| Registry record updated | December 18, 2025 |
| Trial ID | NCT05940350 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are Turkish-speaking adults aged 45 or older with an ischemic stroke, oriented to place/time/person, a Modified Rankin Scale score of 0–3 at discharge, no major communication or cognitive barriers, and access to a phone/email and caregiver support as needed.
✕Probably not a fit
Patients with severe aphasia, dementia or major cognitive impairment, non-vascular or cryptogenic stroke etiologies, severe comorbid or terminal illness, or without phone/internet or caregiver support are unlikely to benefit from this telerehabilitation coaching.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized controlled trial compares usual post-stroke care with a telerehabilitation-based coaching intervention (TeleSCoP). Participants receive an education booklet and one-on-one face-to-face teaching in clinic on day 4–5, set individual goals using motivational interviewing, and are sent educational videos; the intervention includes seven remote coaching sessions over three months with weekly and monthly monitoring and monthly follow-up. Outcomes measured include patient self-efficacy, modifiable vascular risk factors (blood pressure, lipids, triglycerides, HbA1c, BMI, smoking, alcohol) and repeat hospitalizations. The program is delivered in Turkish and requires phone or email access for remote contacts.
Why it matters
Potential benefit: If successful, the program could boost patients' confidence in managing recovery, improve cardiovascular risk factors, and reduce the likelihood of rehospitalization.
How similar studies have gone: Prior telerehabilitation and coaching studies after stroke have shown promising gains in function and self-management, but evidence for durable risk-factor control and reductions in rehospitalization is mixed.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients aged 45 years and older who had a stroke (the etiology of ischemic stroke can be seen at an earlier age due to hematological conditions, such as sickle cell anemia, polycythemia vera, factor deficiencies, vasculitis, and arterial dissection). * Comply with TOAST classification criteria * A score of "0,1,2,3" according to the Modified Rankin Scale at discharge * Place, time, person orientation * No communication barrier * Turkish-speaking writer * Having a contact phone (for phone calls) * Support can be obtained from first-degree situations) * Having no barriers to answering questions physically and mentally Exclusion Criteria: * Stroke of cryptogenic (etiology unknown) or non-vascular origin (tumor) * Have a diagnosed mental or psychiatric illness\* * With dementia and cognitive deficit\* * Clinically musculoskeletal or other neurological diseases\* * With severe aphasia and dysarthria\* * With terminal illness\* * Those who score ≥ 10 according to the LACE index * Patients whose information cannot be accessed will not be included in the study.
Where it's running
-
Akdeniz University Hospital
Antalya, Turkey (Türkiye) Recruiting
Study contacts
- Principal investigator: Hicran Bektas, PhD, RN — Akdeniz University
- Study coordinator: Kamile Topcu, MSc
- Email: kamile-m@hotmail.com
- Phone: +905418651989
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
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.
-
Remote ischemic conditioning for post-stroke insomnia
A 136-person, randomized study will test whether a non-invasive arm-cuff procedure done twice daily for 90 days can improve sleep after a first ischemic stroke in adults 18–80.
-
Ear-based nerve stimulation to help sleep after a stroke
A device that delivers vagal nerve stimulation through the ear is tested to see if it helps stroke patients in rehab sleep better.
-
Theta Burst Stimulation to Help Stroke Recovery (Upper and Lower Limbs)
This trial tests whether applying theta burst stimulation to the motor cortex, in combination with standard rehabilitation, helps people over 45 who recently had a first ischemic stroke recover arm and leg movement.
-
Preventing another ischemic stroke with a smart bracelet and app
This study tests whether a digital prevention program using a wearable and a mobile app can help people who recently had an ischemic stroke reduce the chance of another stroke and improve risk-factor control.
-
Photon-counting CT to check intracranial stents
This study tests whether ultra-high-resolution photon-counting CT can reliably visualize intracranial stents and detect in-stent restenosis during follow-up of patients with prior stents.
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.