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RecruitingNCT06859021Reg-HARUpdated Sep 8, 2026

Validation of the HAR Score for Prioritization of Patients Calling the Emergency Medical Service for Chest Pain by Emergency Call Dispatcher

An observational study in Chest Pain, sponsored by Centre Hospitalier le Mans. Recruiting at 3 sites in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-08.

Sponsored by Centre Hospitalier le Mans · Observational

From the registry’s dates

  • Started Dec 2025; still recruiting 11 months later.
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
796
Ages
18 Years and older
Sex
All
01

Study summary

The lifetime prevalence of chest pain in the general population is 20-40%. The etiologies to be evoked from the outset of management are those of cardiovascular origin, such as acute coronary syndrome (ACS) and pulmonary embolism. ACS is responsible for almost 20% of deaths. Delay in treatment is a major prognostic factor, given the importance of coronary reperfusion.

In France, one of the first contacts with the healthcare system is the medical regulation assistant (MRA) at the Centre 15. His or her role is to prioritize the call according to the identification of immediate signs of seriousness, and if necessary, to decide autonomously to send a rescue team before medical regulation. Depending on the reason for the call and any signs of seriousness, it prioritizes the call according to the expected response time. In line with current recommendations, all calls for chest pain should be answered by an emergency medical dispatcher (EMR) within 5 minutes. However, 60-90% of chest pain calls are not of cardiovascular origin. Their prioritization could therefore be re-qualified for longer response times.

Given the frequency of this type of call, a more efficient MRA referral strategy is needed. To achieve this, decision-support tools would be essential.

The performance of the HAR (History, Age and Risk Factors) score has been recently explored, derived from the HEART score, in a previous single-center prospective study in 2019. It stratifies the risk of a major cardiovascular event (MCE) into low (0 or 1 point), intermediate (2 or 3 points) or high (4, 5 or 6 points).

Investigator's hypothesis is that the HAR score could be entrusted to MRA, to enable them to optimize the prioritization of patients calling with non-traumatic chest pain, by qualifying low-risk chest pain calls on the one hand, which could be prioritized in P2 SNP, and high-risk calls on the other, making it possible to anticipate the dispatch of an emergency service.

02

Conditions studied

  • Chest Pain

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Keywords

  • Chestpain
  • HAR score
  • Emergency call
03

In context

Chest Pain

388 studies on the registry are indexed under Chest Pain; 64 are open to participants now.

This study's planned enrollment of 796 is above the median of 489 across 167 observational studies indexed under Chest Pain.

Browse Chest Pain studies →

Lead sponsor

Centre Hospitalier le Mans is the lead sponsor of 44 studies on the registry; 18 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients calling center 15 for chest pain

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patient of legal age (≥ 18 years)
  • Calling Center 15 from 49, 72 or 37
  • Expressing non-traumatic chest pain, even if this is not the main reason for seeking help.

Exclusion criteria

Exclusion Criteria:

  • Treatment in departments other than 49, 72 and 37
  • Poor understanding of the French language
  • Non-affiliated or non-beneficiary of a social security scheme
  • Person deprived of liberty by judicial or administrative decision
  • Person under forced psychiatric care
  • Person subject to a legal protection measure
  • Person unable to express his/her non-opposition.
  • Follow-up at Day 30 impossible for any reason
  • Person having expressed his/her opposition to the collection of his/her data.
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
796 participants (estimated)
Patient registry
No

Groups and cohorts

  • call for chest pain

    patients who call for chest pain

    Other: follow up call

Interventions

  • Otherfollow up call

    A follow-up call is made to the patient 30 days (+ 5 days) after inclusion to check for the occurrence of an Major Cardio Vascular Event.

06

What researchers measure

Primary outcomes

  1. Number of major cardiovascular events

    Number of major cardiovascular events is measured by presence of Death from cardiological causes, Type 1 or 2 myocardial infarction, Percutaneous coronary intervention, Surgical coronary bypass surgery

    Time frame: 30 days

Secondary outcomes

  1. Performance of the HAR Score: Sensitivity, Specificity, and Comparison Between EMR and MRA

    Sensitivity, specificity, likelihood ratios of the HAR score at different decision thresholds and the area under the ROC curve, as well as reclassification rates between the evaluation of the HAR score by the EMR (Emergency Medical Dispatcher) and the MRA (Medical Regulation Assistant)

    Time frame: From Day 0 to Day 30

  2. Comparaison between rescue resources decided and predicted by the HAR score

    The proportion of rescue resources (SMUR - VSAV...) that would have been decided according to the HAR score (≥ 4 points) compared to the proportion of rescue resources actually decided upon

    Time frame: From Day 0 to Day 30

  3. Time delta between the end of the MRA's score suggesting the dispatch of equipment (HAR score ≥ 4 points) and the actual decision to dispatch equipment in the current situation.

    Time frame: From Day 0 to Day 30

  4. Area under the ROC curve and Delong-Delong test

    Time frame: From Day 0 to Day 30

07

Study locations

3 of 3 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06859021
Lead sponsor
Centre Hospitalier le Mans
Responsible party
Sponsor
First posted
Mar 5, 2025
Start date
Dec 1, 2025
Primary completion
Jun 1, 2027 (estimated)
Completion
Jul 1, 2027 (estimated)
Last update
Sep 8, 2026

Study contacts

Christelle JADEAU
Contact
cjadeau@ch-lemans.fr
+33244710781
Cyrielle HOUALARD, MD
Contact
choualard@ch-lemans.fr
+33243434343

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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