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Not yet recruiting NCT07726628

The Impact of Telemedicine, Using the Caller's Mobile Phone Camera, on the Quality of Care Provided to Adult Patients Contacting the 15 Centre for Acute Dyspnea

No phase Interventional Dyspnea

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Addition of telemedine to standard medical dispatching process.
Who it may be relevant to
Registry conditions: Dyspnea. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Dyspnea is the subjective sensation of difficult or uncomfortable breathing. It accounts for approximately 10% of emergency department visits and 8% of calls to Emergency Medical Communication Centers. Nearly half of patients presenting with dyspnea require hospital admission, 15% require ventilatory support, and approximately 5% die. Early recognition of signs of respiratory severity is therefore essential to accurately assess clinical urgency, guide diagnostic evaluation, and inform appropriate management decisions. In France, patients are encouraged to contact an Emergency Medical Communication Centers before presenting to an emergency department. Calls are managed by an emergency physician responsible for medical regulation, who performs a remote clinical assessment and determines the most appropriate level of care. Depending on the clinical evaluation, the physician may provide medical advice, refer the patient to an emergency department, dispatch emergency medical services, or send a physician-staffed mobile intensive care unit for life-threatening emergencies. The remote assessment of patients presenting with dyspnea is particularly challenging. The inability to directly observe or examine the patient, combined with the caller's difficulty in accurately describing the clinical situation, may impair the recognition of disease severity and result in inappropriate triage decisions, including under-triage and over-triage : Under-triage, characterized by failure to dispatch appropriate emergency resources or to refer the patient to an emergency department when indicated, may delay treatment and increase the risk of adverse outcomes, including mortality. Conversely, over-triage, defined as unnecessary referral to primary care or emergency departments or inappropriate dispatch of emergency resources, contributes to emergency department overcrowding, inefficient use of prehospital resources, and increased healthcare costs. In a previous study, we demonstrated that video-assisted medical triage improved emergency physicians' ability to assess the severity of patients presenting with acute dyspnea. This telemedicine tool enables real-time transmission of a live video stream from the caller's smartphone camera to the emergency physician through a secure digital platform, providing direct visualization of the patient's clinical condition. By enhancing remote clinical assessment, video-assisted triage has the potential to reduce both under-triage and over-triage. In the present stepped-wedge cluster randomized trial, we hypothesized that incorporating real-time video support into the medical regulation of adult patients contacting an Emergency Medical Communication Centers for acute dyspnea would improve the quality of medical decision-making compared with standard telephone triage alone.

Interventions

  • Other Addition of telemedine to standard medical dispatching process
    Patients included during the intervention phase will undergo video-assisted medical triage. Video-assisted triage will be performed using a secure web-based telemedicine hosted on a certified health data server. The emergency physician responsible for medical regulation will send a secure web link via SMS to the caller's smartphone or, when appropriate, to the smartphone of a relative or bystander. Once the link has been activated, a live video stream captured by the smartphone camera will be s

Primary outcome measures

  • To determine whether the use of video-assisted medical triage improves the quality of medical decision-making during the regulation of adult patients contacting Emergency Medical Communication Center with acute dyspnea [Time frame: 28 days]
Secondary outcome measures (8)
  • To compare patients managed with and without video-assisted medical triage with respect to the proportion of patients experiencing under-triage [Time frame: 28 days]
  • To compare patients managed with and without video-assisted medical triage with respect to the proportion of patients experiencing over-triage [Time frame: 28 days]
  • To compare patients managed with and without video-assisted medical triage with respect to the proportion of patients requiring advanced respiratory support (defined as any oxygenation or ventilatory support beyond conventional oxygen therapy) [Time frame: 3 hours, 24 hours, 28 days]
  • To compare patients managed with and without video-assisted medical triage with respect to the proportion of patients admitted to an intensive care unit [Time frame: 24 hours]
  • To compare patients managed with and without video-assisted medical triage with respect to the proportion of patients experiencing cardiac arrest [Time frame: 3 hours, 24 hours, 28 days]
  • To compare patients managed with and without video-assisted medical triage with respect to all-cause mortality [Time frame: 3 hours, 24 hours, 28 days]
  • To compare patients managed with and without video-assisted medical triage with respect to the total duration of the medical regulation process [Time frame: Immediately after the procedure]
  • Medical economic impact: cost-effectiveness study (difference in costs divided by the difference in effectiveness: cost/serious complication avoided) [Time frame: 28 days]

Eligibility criteria

Inclusion criteria

  • Patients aged 18 or over
  • Contacting the Emergency Medical Communication Center regarding acute dyspnea, respiratory distress or shortness of breath, as the main reason for the call, regardless of the underlying cause
  • The patient or a bystander must have a mobile phone equipped with a camera and capable of making video calls
  • Emergency inclusion authorized by the emergency physician responsible for medical regulation in accordance with the emergency consent procedure applicable at the time of the call

Exclusion criteria

  • An immediate life-threatening emergency justifying the dispatch of an emergency response team on an automatic basis in accordance with local protocols
  • Patient at the end of life or where a decision to limit treatment is known at the time of the call.
  • Refusal to use telemedicine
  • Lack of a telephone network enabling video consultation.
  • Patient already included in the study.
  • Individuals requiring enhanced protection, namely minors, pregnant or breastfeeding women, persons deprived of their liberty by a judicial or administrative decision, and adults under legal guardianship known at the time of the call

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Diagnostic

Study locations

France · 1 center
  • University Hospital of Poitiers — Poitiers

Identifiers

NCT: NCT07726628 · 2026-A00879-42

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗