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Ankle Trauma: an Emergency Nurse Assessment Study (ATENA)

Primary Purpose

Ankle Injuries, Foot Injuries, Diagnosis

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Diagnosis and treatment
Sponsored by
University Hospital, Grenoble
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Ankle Injuries focused on measuring Ankle, Foot, Injuries, Ottawa Rules, nurse

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Isolated Ankle and/or foot Trauma out of dermabrasion
  • Admission to emergency department < 48 hours after the trauma
  • Written informed consent must be obtained
  • For women of childbearing age: effective contraception in place for at least 3 months

Exclusion Criteria:

  • X-ray performed before patient admission
  • Obvious open fracture
  • Ankle fracture or obvious deformation
  • Suspicion of polytrauma
  • Anterior surgery of the ankle and/or foot
  • Excessive alcoholization or intoxication by other psychoactive substances
  • Persons unable to communicate in french, with impaired comprehension skills and consciousness (problem with mental health)
  • Adults legally protected (under judicial protection, guardianship, or supervision), persons deprived of liberty
  • Non-affiliated to the french social security system (or equivalent)
  • Pregnant or nursing women
  • Patient participating in any interventional clinical reserach study

Sites / Locations

  • Grenoble Alpes University HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Patient admitted for Ankle and foot injuries

Arm Description

Diagnosis and treatment of Ankle and foot injuries by an accelerated nursing branch in emergency department

Outcomes

Primary Outcome Measures

Percentage of patients who have received a diagnosis and treatment in accordance with medical recommendations.
Percentage of patients who have received a diagnosis and treatment by nurse in accordance with medical recommandation

Secondary Outcome Measures

Percentage of patients with diagnosis in accordance with Ottawa rules
Percentage of patients managed by nurse with diagnosis in accordance with Ottawa rules
Description of pain intensity
Pain intensity assessed by a Numerical Scale ranges (0-10) during admission, on arrival in care areas and during discharge
Deadline for return to work and /or sports
delay (number of days) between the trauma and return to work and/ sports
Consummation of care (excluding medicines)
number of possible consultation after emergency discharge and 30 days
Evaluate the time required to manage patients
Mean length of stay (MLD) in emergency department compared to the MLD of a historical cohort of patients admitted to emergency department for ankle and foot injuries
Percentage of refusal in participation of the study
Percentage of patients screened but who refused to participate in the study
Patient satisfaction assessed during discharge and in one month
Patient satisfaction assessed during discharge and in one month evaluated by visual analog scale (VAS) during discharge and in one month. The VAS scale ranges are: (Not at all satisfied patientwould no longer accept a nurse's care - Completely satisfied patient would accept to be cared for again by a nurse)

Full Information

First Posted
October 1, 2019
Last Updated
April 25, 2023
Sponsor
University Hospital, Grenoble
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1. Study Identification

Unique Protocol Identification Number
NCT04126837
Brief Title
Ankle Trauma: an Emergency Nurse Assessment Study
Acronym
ATENA
Official Title
Accelerated Nursing Branch for the Diagnosis and Treatment of Ankle and Foot Injuries in Emergency Department: Preliminary Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 5, 2020 (Actual)
Primary Completion Date
March 5, 2024 (Anticipated)
Study Completion Date
April 5, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Grenoble

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The ankle and/or foot injuries incidence is high. Lateral ankle sprains are most common diagnosis, while fractures represent less than 15% of final diagnosis. Ankle and/or foot injuries are associated with significant morbidity in terms of pain and chronic instability. The societal cost of these injuries is significant mainly related to hospital care and sick-leave. In summary ankle and/or foot injuries are very frequent reason for emergency admission. The study hypothesis is that an accelerated nursing care system for traumatized ankle and/or foot patients is feasible and allows patients to be cared for in accordance to current medical recommendations. Such a branch should be followed by a return to work and sports within a time frame consistent with the literature. The duration of patient management in emergency department should be short, less than that observed in a historical cohort. Finally patient satisfaction should be high. In the medium term, the implementation of an accelerated nursing branch for the diagnosis and treatment of ankle and/or foot injuries should contribute to effective care and reduction of over activity in emergency departments.
Detailed Description
The incidence of ankle and/or foot injuries is high. Lateral ankle sprains are the most common diagnosis, while fractures represent less than 15% of the final diagnosis. Ankle and/or foot injuries are associated with significant morbidity in terms of pain and chronic instability. The societal cost of these injuries is significant mainly related to hospital care and sick-leave. Ankle and/or foot injuries are very frequent reason for emergency admission. The aim of this study is to assess the accelerated nursing branch for the diagnosis and treatment of ankle and/or foot injuries in emergency department. Target Follow-Up duration: 1 month (30 days). The study will be conducted in 3 phases: Training volunteer emergency department nurses. The training course of 10-hours session (2 hours e-learning and 8 hours attendance) will cover all aspects of management of ankle and/or foot injuries (from diagnosis to treatment). The nurses will have at least one year of clinical experience in emergency department. This training will be conducted by medical experts (emergency doctor, radiologist and orthopedist ). At the end of the training a formative assessment both theoretical and practical will be carried out with participants. The following intervention will be performed by emergency nurses: Pain intensity assessment Record of the trauma mechanism and history of the patient Ottawa rules and clinical examination Radiographic prescription and interpretation Prescription and interpretation of additional examination Foot and Ankle Survey (FAO) Evaluation of ankle joint function Treatment: medicine prescription, immobilization, physiotherapy…. Following the management of ankle and/or foot injuries patients by a nurse, every working day a systemic review of the emergency file including X-rays performed will be carried out by a medical staff composed of an emergency doctor, an orthopedist and a radiologist. This review will be done every morning in the emergency department. Enroll patients admitted to the emergency department for ankle and/or foot injuries. The ability of trained nurses to treat these traumas will be assessed. Phone follow-up of patient after one month to collect data: the date of return to work or sports, patient satisfaction and possible consultation (by a physician, an orthopedist and/or care consummation). Two groups of data will be collected: clinical and paraclinical parameters. Clinical parameters: respiratory rate, saturation, blood pressure, heart rate, Glasgow score , weight, size, Numerical Scale ranges of pain , Ottawa rule, treatment, radiography.. Paraclinical parameters: radiography examination, X-ray interpretation, Foot and Ankle Survey(FAS), Evaluation of ankle joint function, patient satisfaction survey, follow-up at one month (30 days). Outcome measure The overall adequacy of care will be assessed at the end of the study by a committee of experts whose judgment will be based on the latest medical recommendations. This expert committee will consist of an orthopedic physician, a radiologist, an emergency physician and a quality health executive (nurse) and will make decisions by consensus. These members will be independent of the investigators of the study. The delivered care will be considered globally adequate if it respects the recognized indications of: Realization and interpretation of radiography (Ottawa criteria and early radiography service protocol) analgesic treatments according to the recommendations of the scientific societies (acetaminophen for EN> 0 +/- WHO step 2 treatment for pain of moderate intensity and WHO step 3 for pain of severe intensity) Immobilization: according to the recommendations of the scientific societies: protocol RICE (Rest, Ice,Compression and elevation) immobilization plastered in case of fracture etc. Specialist advice: orthopedic opinion if a fracture or other severe pathology is detected Study design • Estimation enrollment: 66 participants A sample of 60 patients can be used to estimate an adequate percentage of care tending towards 100% (optimal management defined by the experts), with an accuracy of 5% corresponding to the lower limit of the one-sided confidence interval. 95% (PASS vs 15.0.5., NCSS, LLC, Kaysville, Utah, USA). This is equivalent to establishing 95% non-inferiority using an exact one-sided test with a power of 80% (Normal approximation). A rate of patients lost to follow-up estimated at 10% implies that 66 patients will have to be included. Analysis: The main objective of this pilot study is to assess the feasibility of managing ankle or foot trauma by an emergency nurse protocol, describing the percentage of patients who are adequately cared for by this protocol. Statistical methods will therefore be essentially descriptive. The descriptive analysis will cover all the variables collected. The quantitative parameters for which normality has been accepted will be described by mean and standard deviation. They will be expressed as median, 25th and 75th percentiles when normality has been rejected. The qualitative parameters will be expressed in numbers and percentages framed by their 95% confidence interval. Serious Adverse events The individual risk is related to a possible misdiagnosis of the nurse who took care of the patient, requiring a further consultation with a general practitioner or emergency. A systematic re-reading of x-rays by the daily medical staff is planned in working days. Patients will be contacted directly by an emergency doctor to advise them to consult their treating or specialist doctor, in case of anomaly detected during the re-reading of the radiography and / or a marked adequacy on the immobilization techniques. In addition, the following adverse events are likely to occur, related to the management of on-trial trauma care: Complications related to limb immobilization (venous thrombosis, eschar, nerve and/or vascular compression) Complications related to analgesics Given the purpose of the research and the low risk associated with the investigation procedures, no monitoring committee and no interim analysis are planned. In the event of a security alert, the expert committee will inform the promoter. In the event of an adverse event considered to be severe by the investigator and possibly involving the health of the subjects, the investigator may stop the study in agreement with the promoter.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ankle Injuries, Foot Injuries, Diagnosis, Treatment
Keywords
Ankle, Foot, Injuries, Ottawa Rules, nurse

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
66 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Patient admitted for Ankle and foot injuries
Arm Type
Other
Arm Description
Diagnosis and treatment of Ankle and foot injuries by an accelerated nursing branch in emergency department
Intervention Type
Other
Intervention Name(s)
Diagnosis and treatment
Other Intervention Name(s)
Assessment of an accelerated nursing branch for the diagnosis and treatment of ankle and/or foot injuries in emergency department.
Intervention Description
Monocentric, Prospective and Biomedical Research excluding Health Product
Primary Outcome Measure Information:
Title
Percentage of patients who have received a diagnosis and treatment in accordance with medical recommendations.
Description
Percentage of patients who have received a diagnosis and treatment by nurse in accordance with medical recommandation
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Percentage of patients with diagnosis in accordance with Ottawa rules
Description
Percentage of patients managed by nurse with diagnosis in accordance with Ottawa rules
Time Frame
1 day
Title
Description of pain intensity
Description
Pain intensity assessed by a Numerical Scale ranges (0-10) during admission, on arrival in care areas and during discharge
Time Frame
1 day
Title
Deadline for return to work and /or sports
Description
delay (number of days) between the trauma and return to work and/ sports
Time Frame
30 days
Title
Consummation of care (excluding medicines)
Description
number of possible consultation after emergency discharge and 30 days
Time Frame
30 days
Title
Evaluate the time required to manage patients
Description
Mean length of stay (MLD) in emergency department compared to the MLD of a historical cohort of patients admitted to emergency department for ankle and foot injuries
Time Frame
30 days
Title
Percentage of refusal in participation of the study
Description
Percentage of patients screened but who refused to participate in the study
Time Frame
30 days
Title
Patient satisfaction assessed during discharge and in one month
Description
Patient satisfaction assessed during discharge and in one month evaluated by visual analog scale (VAS) during discharge and in one month. The VAS scale ranges are: (Not at all satisfied patientwould no longer accept a nurse's care - Completely satisfied patient would accept to be cared for again by a nurse)
Time Frame
1 and 30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Isolated Ankle and/or foot Trauma out of dermabrasion Admission to emergency department < 48 hours after the trauma Written informed consent must be obtained For women of childbearing age: effective contraception in place for at least 3 months Exclusion Criteria: X-ray performed before patient admission Obvious open fracture Ankle fracture or obvious deformation Suspicion of polytrauma Anterior surgery of the ankle and/or foot Excessive alcoholization or intoxication by other psychoactive substances Persons unable to communicate in french, with impaired comprehension skills and consciousness (problem with mental health) Adults legally protected (under judicial protection, guardianship, or supervision), persons deprived of liberty Non-affiliated to the french social security system (or equivalent) Pregnant or nursing women Patient participating in any interventional clinical reserach study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Damien VIGLINO, MD,PhD
Phone
0033476766784
Email
DViglino@chu-grenoble.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Prudence MABIALA MAKELE, PhD
Phone
0033476766784
Email
pmabialamakele@chu-grenoble.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Damien VIGLINO, MD,PhD
Organizational Affiliation
Emergency Department of University Hospital Grenoble
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Nicolas TERMOZ MASSON, Bachelor
Organizational Affiliation
Emergency Department of University Hospital Grenoble
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Alexandra BICHET, Bachelor
Organizational Affiliation
Emergency Department of University Hospital Grenoble
Official's Role
Study Director
Facility Information:
Facility Name
Grenoble Alpes University Hospital
City
Grenoble
State/Province
Isere
ZIP/Postal Code
38043
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Damien VIGLINO, MD, PhD
Phone
0033476766784
Email
DViglino@chu-grenoble.fr
First Name & Middle Initial & Last Name & Degree
Damien VIGLINO, MD, PhD
First Name & Middle Initial & Last Name & Degree
Batistin MARTINON, MD
First Name & Middle Initial & Last Name & Degree
Jérôme TONETTI, Professor PhD
First Name & Middle Initial & Last Name & Degree
Gilbert FERRETTI, Professor PhD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The international writing and publication rules (The Uniform Requirements for Manuscripts of the ICMJE, April 2010) will be followed. The minimum anonymized source data for performing the statistical analysis will be made public at the time of publication, with the article, or deposited in an appropriate public database. Other anonymized data may be available from the principal investigator upon reasonable request and with the consent of the sponsor. In accordance with the French law n ° 2002-303 of March 4th, 2002, the subjects can be informed, at their request, of the overall results of the research. In this study, the investigators commit to individually communicating the overall results to each subject participating in the research by a short (popularized) summary and associated with a copy of the scientific article.
IPD Sharing Time Frame
at the time of publication
IPD Sharing Access Criteria
The international writing and publication rules (The Uniform Requirements for Manuscripts of the ICMJE, April 2010) will be followed. And In accordance with the French law n ° 2002-303 of March 4th, 2002

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Ankle Trauma: an Emergency Nurse Assessment Study

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