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A 'digital-first' approach is currently under implementation in several Swedish regions.
The principles behind implementing an online service as an access way to primary care are based on an expectation that it can make access easier, direct people to appropriate levels of care, and increase both availability of heath care and cost efficiency. However, a recent Swedish report concluded that digital triage in primary care has not been investigated in a clinical real-world setting, including real patients, meaning that the benefits and risks for patients as well as on a system level remain unclear.
The aim of this trial is to study the feasibility of a larger trial that will compare digital triage and traditional telephone triage on adherence to triaged health care level, in a randomized controlled study (feasibility study, RCT). The study will recruit a total of 120 patients, of which half will be randomized to telephone triage and half to digital triage.
Full description
Ten regions in Sweden are currently collaborating in the implementation of a new digital platform for digital symptom assessment and triage.
The patient's path is as following:
Study design
Design: Feasibility study, randomized controlled study Patients: Patients referred by the online symptom checker to digital triage with a nurse and patients receiving traditional telephone triage. This study is planned to be carried out at one or more health centers where both traditional telephone triage and digital triage are used. The study will be conducted initially as a feasibility study with 30 participants in each arm and the inclusion period will continue until this number is met. A larger RCT is planned in the future, based on the feasibility study. The consent to participate will be filled in electronically by the participants in the digital triage group, and by the nurse in the telephone group (and documented in the electronic medical record).
Enrollment
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Inclusion criteria
Exclusion criteria
Patients <18 years or parents seeking advice for their children
Primary purpose
Allocation
Interventional model
Masking
120 participants in 2 patient groups
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Central trial contact
Veronica V Milos Nymberg, PhD
Data sourced from clinicaltrials.gov
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