Key result
The ACQUIRE-ICD trial is a planned randomized controlled trial that will evaluate the effectiveness of a comprehensive interactive eHealth intervention on device acceptance in 478 patients with a first-time ICD.
Why the study?
Does a comprehensive interactive eHealth intervention improve device acceptance in patients receiving a first-time ICD or CRT-D?
RCT (n=478)
Unblinded
1:1, stratified by center and heart failure symptom severity
Yes
Does a comprehensive interactive eHealth intervention improve device acceptance in patients receiving a first-time ICD or CRT-D?
This study protocol outlines a randomized controlled trial to evaluate whether a comprehensive eHealth intervention improves device acceptance and clinical outcomes in patients receiving their first ICD or CRT-D.
BACKGROUND: In Denmark and other countries, there has been a shift in the management of patients with an implantable cardioverter defibrillator (ICD) with remote device monitoring largely replacing in-hospital visits. Less patient-nurse and patient-physician interaction may lead to gaps in patients' quality of care and impede patients' adaptation to living successfully with the ICD. A comprehensive eHealth intervention that include goal-setting, monitoring of symptoms of depression, anxiety, and quality of life, psychological treatment, information provision, supportive tools, online dialogues with nursing staff and access to an online community network, may help fill these gaps and be particularly beneficial to patients who suffer from anxiety and depression. This study will evaluate the effectiveness of the ACQUIRE-ICD care innovation, a comprehensive and interactive eHealth intervention, on patient-reported and clinical outcomes. METHODS: The ACQUIRE-ICD study is a multicenter, prospective, two-arm, unblinded randomised controlled superiority trial that will enroll 478 patients implanted with a first-time ICD or ICD with cardiac synchronisation therapy (CRT-D) from the six implanting centers in Denmark. The trial will evaluate the clinical effectiveness and cost-effectiveness of the ACQUIRE-ICD care innovation, as add-on to usual care compared with usual care alone. The primary endpoint, device acceptance, assessed with the Florida Patient Acceptance Survey, is evaluated at 12 months' post implant. Secondary endpoints, evaluated at 12 and 24 months' post implant, include patient-reported outcomes, return to work, time to first ICD therapy and first hospitalisation, mortality and cost-effectiveness. DISCUSSION: The effectiveness of a comprehensive and interactive eHealth intervention that relies on patient-centred and personalised tools offered via a web-based platform targeted to patients with an ICD has not been assessed so far. The ACQUIRE-ICD care innovation promotes and facilitates that patients become active participants in the management of their disease, and as such addresses the need for a more patient-centered disease-management approach. If the care innovation proves to be beneficial to patients, it may not only increase patient empowerment and quality of life but also free up time for clinicians to care for more patients. TRIAL REGISTRATION: The trial has been registered on https://clinicaltrials.gov/ct2/show/NCT02976961 on November 30, 2016 with registration number [ NCT02976961 ].
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Pedersen et al. (2018) conducted an RCT in Implantable cardioverter defibrillator (ICD) or CRT-D (n=478). ACQUIRE-ICD comprehensive interactive eHealth intervention vs. Usual care was evaluated on Device acceptance (Florida Patient Acceptance Survey) at 12 months. The ACQUIRE-ICD trial is a planned randomized controlled trial that will evaluate the effectiveness of a comprehensive interactive eHealth intervention on device acceptance in 478 patients with a first-time ICD.
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