Clinical Trials Logo

Clinical Trial Summary

In 2020 an independent evaluation of the Zio service as part of the Digital Health Technologies programme at NICE was conducted. From the available clinical and economic evidence, the evaluation concluded that further evidence is needed to estimate the resource use associated with Zio compared with standard care, particularly the number of outpatient visits and repeat testing needed. Additionally it recommended further evidence is needed for the longer-term clinical consequences such as anticoagulant uptake and other changes to treatment related to the results from monitoring. (MTG52) Therefore, this study aims to address these uncertainties and identify whether the Zio service could be used in the health and social care system in England. This will be assessed using a multicentre, cohort study design consisting of two cohorts. The data for the existing standard of care cohort using Holter monitor (cohort 1) will be collected from 6-month retrospective pre-covid data, and, for the Zio service cohort (cohort 2), data will be collected retrospectively over a 6-month period. Each cohort will include two separate populations recruited from cardiology clinics and stroke/TIA clinics. The main objective of this study is to analyse quantitative data collected from participating sites and complementary qualitative data on Zio utilisation from questionnaires


Clinical Trial Description

The proposed study is a multi-centre, cohort study that will collect 6-month control data from a cohort of participants wearing Holter devices (2018-2019) and match this data to a 6-month cohort of patients wearing Zio patches (2021 - 2022). An additional cohort of patients using the Zio patch from both the cardiology and stroke/TIA population will be included for the patient experience aspect of the study. Other designs have been considered but from a pragmatic point of view and the need for a "real-world" evaluation this is the preferred alternative with the caveat that there may not be an exact match between the two patient groups. The proposed study is a multi-centre, cohort study that will collect 6-month baseline data from a retrospective cohort of participants wearing Holter devices and match this data to a 6-month retrospective cohort of patients wearing Zio patches. Zio is standard of care at the NHS sites participating in this study, but it is not standard of care across the NHS. The standard of care received by patients involved in this study will not be affected by their participation in the study. However, should Zio be adopted more widely by the NHS, a change in pathway will be required. The Zio device is CE marked as a Class IIa and will be used within its intended purpose. Two separate populations will be considered for this study: cardiology outpatients and patients at risk of (or who have had a previous) stroke or TIA. Each of these populations will comprise a control cohort for Holter monitor and a cohort for Zio service, which will be analysed separately. A separate cohort comprising of participants prescribed Zio will be included in a qualitative analysis to assess their experience of using Zio and previous experience of using Holter monitor within the past 2 years, where applicable. This will allow for a comparative analysis of patient experience. For patients in the cohort who have not had prior experience of using Holter monitor, a questionnaire will be administered to assess their experience of using Zio only. Given the potential for a shift in the spectrum of the population that may be expected when Zio is implemented, propensity score matching will be utilised to compare the Holter and Zio cohorts for both the stroke/TIA and cardiology arms. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05560828
Study type Observational
Source King's College London
Contact Anna Barnes
Phone 020 784 89527
Email anna.barnes@kcl.ac.uk
Status Not yet recruiting
Phase
Start date October 31, 2022
Completion date December 31, 2022

See also
  Status Clinical Trial Phase
Completed NCT01212978 - Overcoming Inactivity in Older Adults: Impact on Vascular Homeostasis N/A
Recruiting NCT05885113 - Developmental Intervention for Hospitalized Newborns With Congenital Heart Disease N/A
Not yet recruiting NCT05369728 - Screening Of CoRonary ArTEry diSease N/A
Not yet recruiting NCT05306730 - Echocardiography by Non-cardiologist in Early Management of Patients With Chest Pain N/A
Terminated NCT03800862 - The Evaluation of the Roles of New Cardiac Imaging in Patients With Chest Pain
Completed NCT06265610 - A Comparison Of The Effect Of Target-Controlled Infusion Anesthesia And Inhalation Anesthesia
Completed NCT02906423 - Results From a Health System-wide Implementation of a Quality of Life Questionnaire N/A
Completed NCT03523247 - A Whole Food Plant Diet and Its Lipidemic Effects on Primary Prevention in a Free-range Population N/A
Active, not recruiting NCT06277323 - UCLA Health Patient Cardiology Care Gaps N/A
Active, not recruiting NCT04806204 - Music Therapy in Coronary Angiography N/A
Recruiting NCT02778724 - France PCI Registry : National Observatory of Interventional Cardiology
Recruiting NCT04243226 - Effects of Aerobic Exercise on Cognition,Cerebral Brain Flow and Mental Health Among Traumatic Brain Injury Patients N/A
Terminated NCT05461599 - Digital Therapeutic for Adolescent Depressive Symptoms in Cardiology and Gastroenterology N/A
Not yet recruiting NCT01682122 - Frequency and Persistence of Wide Pulse Pressure in the Neonatal Population N/A
Completed NCT00503126 - Bivalirudin as a Procedural Anticoagulant in Pediatrics Phase 2
Completed NCT04967261 - The Evaluation of Optimal Observation Period for Neurological Recovery in Post-arrest Survivors
Recruiting NCT04913207 - Comprehensive CT-guided vs Echo-fluoroscopy-guided Strategy in the Left Atrial Appendage Occlusion N/A