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Unscheduled CareCSNP68NCT05835908

Follow-up of Patients Referred to Unscheduled Care Centers by the Emergency Call Center in the Haut-Rhin Department, France

An observational study of Unscheduled Care, run by Groupe Hospitalier de la Region de Mulhouse et Sud Alsace at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The objective of this study is to determine the follow-up of patients who were referred by the Emergency Call Center of the Haut-Rhin department to an Unscheduled Care Centers (UCC) and to determine whether they actuallly went to a UCC following their call, or if they were taken in charge by another care facility. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Unscheduled Care
What is being tested?
Phone questionnaire
How many people
100 participants
Where
1 siteFrance
Study dates
17 May 2023to 13 Jun 2023
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Adult, Older adult

Study population: Patient who contacted the Emergency Call Center and were referred to an Unscheduled Care Center.

Who may be able to join

  • Call to the Emergency Call Centre of the Haut-Rhin department by an adult (age ≥ 18 years)
  • Referral to the Unscheduled Care Center by the Emergency Call Center
  • Non-inclusion criteria:
  • Patient who does not answer phone within 30 days of call to the Emergency Call Center
  • Patient who refuses to participate in the study
  • Call for someone other than him or herself (except when a parent calls for his or her minor child)

Who cannot join

None listed.

Trial locations and contacts

1 site in 1 country.

France1 site
  • GHRMSA

    Mulhouse, Haut-Rhin, 68100

Other trials in France

About this study

The objective of this study is to determine the follow-up of patients who were referred by the Emergency Call Center of the Haut-Rhin department to an Unscheduled Care Centers (UCC) and to determine whether they actuallly went to a UCC following their call, or if they were taken in charge by another care facility.

Read the detailed description

Conduct of research:

Patients who contacted the emergency call center and were referred to an unscheduled care center in the Haut-Rhin will be contacted by mail in the first instance. Ten to fifteen days after the call to the emergency call center, the investigator will contact the patient by phone, during which he/she will ask for the patient's oral consent to participate in the research and collect follow-up data using a standardized questionnaire.

If the investigator is unable to reach the patient, further attempts will be made to call the patient up to 30 days after the initial call. If there is no response after this time, patients will not be included the study.

Being tested
Phone questionnaire

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Phone questionnaireOther

    Patients will be contacted by the investigator to collect information regarding follow-up from the initial call to the Emergency call center until the patient is taken care of in the health care facility to which he/she has been admitted.

Study groups in NCT05835908
Study groupRoleWhat they receive
Patient who contacted the Emergency Call Center and were referred to an Unscheduled Care CenterNot described
Receives: Other: Phone questionnaire

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Phone questionnaire

    Patients will be contacted by the investigator to collect information regarding follow-up from the initial call to the Emergency call center until the patient is taken care of in the health care facility to which he/she has been admitted. Information will be collected on: time and day of the call to the Emergency call center; reason for call; understanding of the instructions given by the call center agent; delay between the call to the Emergency call centre and the visit to the care facility; and, if applicable, the reason why the patient did not go to the UCC.

    Measured: Up to 30 days following the call to the Emergency call center

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Apr 2023
  2. Study start17 May 2023
  3. Primary completion13 Jun 2023
  4. Study completion13 Jun 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
100 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05835908
Sponsor's protocol ID
GHRMSA 1290
Acronym
CSNP68
Status last verified
Oct 2023
First submitted
19 Apr 2023
Last updated
20 Nov 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Unscheduled Care, run by Groupe Hospitalier de la Region de Mulhouse et Sud Alsace at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 20 Nov 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Phone questionnaire (time frame: Up to 30 days following the call to the Emergency call center). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Nov 2025.

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