A Personalized, Digital Coaching Program After Stroke

NCT03038685 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 148

Last updated 2021-01-14

No results posted yet for this study

Summary

The Belgian Stroke Council initiated a project to improve risk factor control and medication adherence in ischemic stroke patients by developing an individualized in-hospital initiated and post- discharge, digital coaching program addition to standard practice (strokecoach.be).

Conditions

  • Stroke, Ischemic

Interventions

BEHAVIORAL

Strokecoach.be - digital coaching program for stroke patients

The stroke coach gives patients two education sessions during hospitalization (risk factor management, review of medications and clinical evolution). During these sessions, study participation will be proposed. Eligibility will partially depend on their historical use of the internet and e-mail. The aim is to have the digital platform personalized for his/her individual needs, risk factors and remaining neurologic signs/symptoms. Tips and tricks to deal with lifestyle modification will be delivered on regular basis. Meanwhile, patients will be asked to complete on a pre-specified frequency their data regarding their cardiovascular risk profile. Additionally, participants will be contacted at 0.5-1-2 and 6 months by phone calls or videoconsultancy. To standardize, an adapted, digital version of the standardized WSO Post-Stroke Checklist shall be used as a decision-support flowchart. A report of the consultation will be derived after the videoconsultancy.

Sponsors & Collaborators

  • Sint-Lucashospital, Bruges, Belgium

    collaborator UNKNOWN
  • AZ Sint-Jan AV

    collaborator OTHER
  • Groeningehospital, Kortrijk, Belgium

    collaborator UNKNOWN
  • Belgian Stroke Council

    collaborator UNKNOWN
  • Interuniversity Centre For Health Economics Research, VUB, Brussels, Belgium

    collaborator UNKNOWN
  • University Hospital, Antwerp

    lead OTHER

Principal Investigators

  • Peter Vanacker, MD PhD · University Hospital, Antwerp

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-05-01
Primary Completion
2018-02-28
Completion
2018-02-28

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03038685 on ClinicalTrials.gov