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OpenTrials
Completed

NCT Number: NCT06092866

Digital Versus Telephone Symptom Assessment and Triage in Primary Care

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.

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Key information

Conditions

Infections Digestive System Diseases Gastro-Intestinal Disorder Injuries Mental Disorders Psychiatric Disorder Skin Diseases Skin and Connective Tissue Diseases Wounds and Injuries

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Veronica Milos Nymberg

Malmö, Region Skane, 20502, Sweden

About this study

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:

  • Triage to self-care. The patient will start his/her health care contact at the website www.1177.se with mobile bank identification. An algorithm-based computerized symptom checker performs the initial assessment, based on patient's self-reported complains. This initial triage can result in an auto-triage with self-care advice for non-complicated health issues.
  • Triage to digital assessment by chat with a nurse. Patients with more complex needs will be directed to the primary health care center (PHCC) where the patient is listed. There is also a central back-up unit that manages patients during out of office hours. The triage nurse can supplement the patient history with additional questions and finally determine the level of care.
  • Patients in need of further assessment are booked to a physical visit to a doctor or other health care staff, or referral to an emergency room.

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).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 years or older who is listed at the health center

Exclusion criteria

  • Patients <18 years or parents seeking advice for their children
  • Cannot communicate in Swedish or other communication difficulties in language or writing
  • Patients without a mobile Bank identification (to log in to the platform)
  • Administrative issues, e.g. rebooking of time

Treatment and study plan

Digital triage

Behavioral

A registered nurse assesses the symptoms reported by the patient on the online platform and gives appropriate advice for further care using chat.

Other names: Symptom assessment

Primary outcomes

  1. Recruitment rate as percentage of patients included in the study measured using data from the primary health care center

    Time frame: 6 months

    Percentage of patients that accept to be included in the study of all patients that contact the primary care center during the studied period of time

  2. Drop-out rate as percentage of patients that drop-out from the trial

    Time frame: 6 months

    Percentage of patients that drop-out from the trial

  3. Eligibility criteria in percentage of patients being eligible to be included in the study

    Time frame: 6 months

    Age 18 years or older and listed on the primary care center

Secondary outcomes

  1. Adherence to recommended health care level as percentage of patients that adhere to recommended care level

    Time frame: 2 months

    Within 2 months after the triage contact, data collected from the regional data base

  2. Interrater reliability

    Time frame: 2 months

    agreement between the care-level suggested by the online symptom checker and the care-level suggested by the nurse, data collected from the electronic medical journals

Sponsors and collaborators

Lead sponsor

Region Skane

Other

Registry information

Important dates

Study start
2023
Primary completion
2025
Study completion
2026
First posted
Oct 23, 2023
Registry last updated
May 1, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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