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Study identifier: NCT06667505 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

To Test an e-Health Educational Intervention Patients With an ICD

Condition: Implantable Cardioverter Defibrillator (ICD)  ·  Sponsor: University of Ulster

PhaseNA
Planned participants256
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Role of the implantable cardioverter defibrillator (ICD) is to monitor heart rate and discharge a small electrical discharge or shock if the heart rate becomes life threatening. Patients and family members have requested more information about their ICD, how it works and how to live well with the device. This study will build on previous research by designing, in collaboration with patients, family members and professionals, an online resource to provide important information that can lower anxiety and concerns, and improve quality of life. The CHOICE-ICD resource will be easy to use, incorporating games and quizzes to encourage engagement, up to date information appropriate to each patient's needs, as well as animation clips, virtual reality, and short patient videos. CHOICE-ICD will be made available to 64 patients, in addition to normal care, awaiting or with a recently implanted ICD in Belfast and Glasgow. Patients will use the resource for 3 months. Patients and family members will then be asked to complete questionnaires and participate in semi-structured interviews. This study will develop 1st UK online resource providing information to enable patients to have greater choice and control in their care.

This description comes directly from the study's public registry record.

Talk to the study team

Loreena M Prof Loreena M Hill, PhD  ·  +44 7841037404  ·  l.hill@ulster.ac.uk

Lana Dr Lana Dixon, MD  ·  lana.dixon@belfasttrust.hscni.net

Always discuss trial participation with your own doctor first.

Locations (2)

Belfast Health and Social Care TrustBelfast, County Antrim, United KingdomNot Yet Recruiting
Golden Jubilee National HospitalGlasgow, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT06667505