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Accepted for/Published in: JMIR Formative Research

Date Submitted: Feb 21, 2024
Date Accepted: Sep 5, 2024

The final, peer-reviewed published version of this preprint can be found here:

Implementation and User Satisfaction of a Comprehensive Telemedicine Approach for SARS-CoV-2 Self-Sampling: Monocentric, Prospective, Interventional, Open-Label, Controlled, Two-Arm Feasibility Study

Voit F, Erber J, Egert-Schwender S, Hanselmann M, Laxy M, Kehl V, Hoffmann D, Michler T, Protzer U, Jeske SD, Kohlmayer F, Schmid RM, Spinner CD, Weidlich S

Implementation and User Satisfaction of a Comprehensive Telemedicine Approach for SARS-CoV-2 Self-Sampling: Monocentric, Prospective, Interventional, Open-Label, Controlled, Two-Arm Feasibility Study

JMIR Form Res 2024;8:e57608

DOI: 10.2196/57608

PMID: 39661941

PMCID: 11655044

Implementation and user satisfaction of a comprehensive telemedicine approach for severe acute respiratory syndrome coronavirus 2 self-sampling: a monocentric, prospective, interventional, open-label, controlled, two-arm feasibility study

  • Florian Voit; 
  • Johanna Erber; 
  • Silvia Egert-Schwender; 
  • Michael Hanselmann; 
  • Michael Laxy; 
  • Victoria Kehl; 
  • Dieter Hoffmann; 
  • Thomas Michler; 
  • Ulrike Protzer; 
  • Samuel D. Jeske; 
  • Florian Kohlmayer; 
  • Roland M. Schmid; 
  • Christoph D. Spinner; 
  • Simon Weidlich

ABSTRACT

Background:

The universal availability of smartphones has created new opportunities for innovative telemedicine applications in healthcare. The coronavirus disease 2019 (COVID-19) pandemic has heightened the demand for contactless healthcare services, making severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) polymerase chain reaction (PCR) testing a crucial component of pandemic containment.

Objective:

This feasibility study aimed to examine a comprehensive telemedicine approach for SARS-CoV-2 testing.

Methods:

The study process involved shipping self-sampling kits, providing instructions for at-home sample collection, processing biomaterials (swabs, capillary blood), communicating test results, and providing interoperable data for clinical routine and research through a medical mobile app. One hundred individuals were randomly assigned to either the conventional healthcare professional (HCP)-performed SARS-CoV-2 testing group (conventional testing group, CG) or the telemedicine-guided SARS-CoV-2 self-sampling approach (telemedicine group, TG). Feasibility of the TG approach, user satisfaction, user-centered outcomes, and economic aspects were assessed and compared between the groups.

Results:

In the TG group, 47 individuals (95%) received a self-sampling kit via mail. Thirty-seven (76%) individuals successfully returned at least one sample for diagnostics. SARS-CoV-2 PCR tests were conducted in 35 (95%) of TG cases compared to 44 (88%) in the CG. Users in the TG reported high satisfaction levels with ease of use (5.2/7), interface satisfaction (5.2/7), and usefulness (4.3/7). A micro-costing model indicated a slightly higher cost for the TG approach than the CG approach. The TG facilitated interoperable data transmission by providing anonymized, standardized data sets for extraction using health level7-Fast Healthcare Interoperability Resources. This supports the national COVID-19 data exchange platform and facilitates epidemiological evaluation based on the German COVID Consensus dataset.

Conclusions:

Integrating a telemedicine-based approach to SARS-CoV-2 testing into an existing hospital data infrastructure is feasible, creating possibilities for broader use of mobile apps in medical care and potentially promoting future user satisfaction and treatment quality. Clinical Trial: drks.de DRKS00027093


 Citation

Please cite as:

Voit F, Erber J, Egert-Schwender S, Hanselmann M, Laxy M, Kehl V, Hoffmann D, Michler T, Protzer U, Jeske SD, Kohlmayer F, Schmid RM, Spinner CD, Weidlich S

Implementation and User Satisfaction of a Comprehensive Telemedicine Approach for SARS-CoV-2 Self-Sampling: Monocentric, Prospective, Interventional, Open-Label, Controlled, Two-Arm Feasibility Study

JMIR Form Res 2024;8:e57608

DOI: 10.2196/57608

PMID: 39661941

PMCID: 11655044

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