- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05753319
Physiotherapist in the Emergency Department (KiUrge)
May 21, 2024 updated by: Nantes University Hospital
Physiotherapist in the Emergency Department : What Impact Does the Intervention of the Physiotherapist Have on the Care Pathway of the Elderly Person Who Falls?
This study aims to evaluate the impact of assessment and early physiotherapy management on the care pathway of the elderly person who falls, their length of stay in hospital and their fall recurrence rate.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
155
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Loire-Atlantique
-
Nantes, Loire-Atlantique, France, 44093
- University Hospital of Nantes
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
75 years and older (Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
People aged 75 and over admitted to emergency for falls
Description
Inclusion Criteria:
- Patients aged 75 and over
- Patients admitted to emergency for falls.
- Clinically stable patient who may benefit from a gait assessment or fall risk assessment
- Patients able to understand the protocol and not verbally object to participation.
Exclusion Criteria:
- Patients with limb fractures requiring surgical treatment
- Patients under guardianship or curatorship.
- Patients already included in an interventional research protocol.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Physiotherapy group
Intervention group with assessment and early physiotherapy
|
Realization of a physiotherapy assessment.
|
|
Control group
control group without assessment and physiotherapy in the emergency department
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient orientation (return home, short-term hospitalization unit, hospitalization) at discharge from the emergency department
Time Frame: up to 48 hours
|
The orientation of the patient on discharge from the emergency services, according to the three defined pathways (return home, short-term hospitalization unit, hospitalization).
|
up to 48 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Length of stay in emergency departments and in the short stay hospital unit
Time Frame: up to 48 hours
|
Calculation of the duration in hours by recording the dates and times of admission and discharge from the service.
|
up to 48 hours
|
|
Total duration of hospitalization for each stay, all services combined
Time Frame: 1 week
|
Calculation of the duration in hours by recording the dates and times of admission to the emergency services and final discharge from the hospital.
|
1 week
|
|
Number of recurrence of emergency admission for the same reason (fall)
Time Frame: up to 9 days
|
Recurrence of a fall within seven days of returning home
|
up to 9 days
|
|
Satisfaction of doctors in emergency services
Time Frame: 0 day
|
A satisfaction questionnaire will be sent to all doctors who participated in the study
|
0 day
|
|
Emergency discharge referral before and after assessment by the physical therapist.
Time Frame: up to 48 hours
|
For the "Physiotherapy group" : Description of changes in physician orientation decision (return home, acute care unit, hospitalization) of patients, before/after the physical therapist assessment
|
up to 48 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Marie Blandin, Nantes University Hospital
- Principal Investigator: Marie Gallet, marie.gallet@chu-nantes.fr
- Principal Investigator: Guillaume LE SANT, PhD, Laboratoire Motricité, Interactions, Performance (UR 4334)
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 6, 2023
Primary Completion (Actual)
March 14, 2024
Study Completion (Actual)
March 14, 2024
Study Registration Dates
First Submitted
February 10, 2023
First Submitted That Met QC Criteria
February 21, 2023
First Posted (Actual)
March 3, 2023
Study Record Updates
Last Update Posted (Actual)
May 22, 2024
Last Update Submitted That Met QC Criteria
May 21, 2024
Last Verified
May 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RC23_0068
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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