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Fall PatientsNCT06528899

Physiotherapy in Emergency Department: a Service Analysis From a French Hospital

An observational study of Fall Patients and Pain, run by Université de Nantes at 2 sites 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 skills of physiotherapists have been employed to enhance access to optimal care in Emergency Departments (ED). No study has yet been conducted on the practices in France. The primary objective of this study was to describe the French practices of physiotherapy within an ED, and to secondary examine the effect on… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Fall Patients, Pain, Sprains
What is being tested?
Physical Therapy
How many people
461 participants
Where
2 sitesFrance
Study dates
1 Apr 2022to 31 Dec 2022
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
  • No healthy volunteers
  • Adult, Older adult

Study population: All adult patients visiting the Emergency Department

Who may be able to join

  • admission in the Emergency Departement
  • aged over 18
  • refferal for physiotherapy within the Emergency Department

Who cannot join

  • death
  • no admission within the Emergency Department (only administrative purposes)

Trial locations and contacts

2 sites in 1 country.

France2 sites
  • CHU de Nantes

    Nantes

  • Université de Nantes - MIP UR 4334 (Motricity, Movement, Interactions)

    Nantes

Other trials in France

About this study

The skills of physiotherapists have been employed to enhance access to optimal care in Emergency Departments (ED). No study has yet been conducted on the practices in France. The primary objective of this study was to describe the French practices of physiotherapy within an ED, and to secondary examine the effect on patient discharge.

Read the detailed description

A retrospective observational study was conducted on patients who received a referral for physiotherapy in the ED (E-PT) of the Universitarian Hospital of Nantes during a six-month observation period in 2022. A total of 461 medical records were extracted, including patient characteristics and the main chief complaint at the time of admission. Details on the delivery of E-PT were collected, as well as the end status at the exit of the ED. Descriptive statistics were performed to analyse the data. A propensity score analysis examined the association between the patients' status at the exit of the ED and E-PT.

Being tested
Physical Therapy
Keywords
physical therapy, patient pathway, patient care management
Medical subject headings
Pain, Sprains and Strains, Respiratory Insufficiency, Vertigo, Illness Behavior

What participants receive

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

  • Physical TherapyBehavioural

    Assessment and/or treatment by physitoherapist during the visit

Study groups in NCT06528899
Study groupRoleWhat they receive
Emergency Physiotherapy (E-PT)Subcohort of patients receiving a referral + Emergency Physiotherapy (E-PT) during their visit to Emergency Department
Receives: Behavioral: Physical Therapy
control (CTL)Subcohort of patients receiving a referral + but no Emergency Physiotherapy (E-PT) during their visit to Emergency Department

What is being measured

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

  1. Discharge at the exit of ED

    the type of discharge (home / hospitalisation)

    Measured: up to 7 days (date of exit)

Secondary outcomes (1)
  1. Length of stay

    duration of stay in the ED

    Measured: up to 7 days (date of exit)

Timeline

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

  1. First posted30 Jul 2024
  2. Study start1 Apr 2022
  3. Primary completion31 Dec 2022
  4. Study completion31 Dec 2022

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
461 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06528899
Sponsor's protocol ID
KiUrge-retro
Status last verified
Jul 2024
First submitted
17 Jul 2024
Last updated
30 Jul 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: The data that support the findings of this study are available from the corresponding author, \[GLS\], upon reasonable request. The data is not publicly available or to reusable due to privacy and ethical restrictions.

Questions about this trial

What is this clinical trial studying?

An observational study of Fall Patients and Pain, run by Université de Nantes at 2 sites 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 3 inclusion and 2 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 30 Jul 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites 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?

Discharge at the exit of ED (time frame: up to 7 days (date of exit)). 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 30 Jul 2024.

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