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E-learning to Improve Oral Anticoagulant Use in Hospitalized Older People With AF (SIM-AF)

Primary Purpose

Simulation Training, Anticoagulant Drugs, Elderly

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
E-learning educational program
Control
Sponsored by
Mario Negri Institute for Pharmacological Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Simulation Training

Eligibility Criteria

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

Inclusion Criteria:

  • subjects 65 years of age or older, with known or newly diagnosed AF, admitted to the Internal Medicine and Geriatric wards of the REPOSI network,
  • consent to participate to the study.

Exclusion Criteria:

  • consent denial to participate to the study,
  • absolute contraindication to OAC,
  • re-hospitalisation for the subject already included in the study,
  • life expectancy less than 6 months.

Sites / Locations

  • Azienda Ospedaliera Universitaria Policlinico Sant'Orsola Malpighi
  • Istituto Fondazione Poliambulanza
  • Policlinico Universitario Mater Domini
  • AO Universitaria Policlinico di Modena
  • Azienda Ospedaliera S. Gerardo di Monza
  • Ospedale degli Infermi
  • Azienda Ospedaliera Universitaria - Ospedale Riuniti
  • A.O. Ospedale di Circolo e Fondazione Macchi
  • Azienda Consorziale Ospedaliera Policlinico
  • Azienda Ospedaliera Papa Giovanni XXIII
  • Azienda Ospedaliera Universitaria "Policlinico Vittorio Emanuele"
  • Azienda Ospedaliera Universitaria San Martino - IST
  • Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
  • Azienda Ospedaliera di Padova
  • Azienda Ospedaliera Universitaria Policlinico P. Giaccone
  • Azienda SocioSanitaria Territoriale, Ospedale Civile "C.Mira" di Casorate Primo
  • Policlinico San Matteo
  • Ospedale San Giovanni Calibita Fatebenefratelli
  • Policlinco Universitario Agostino Gemelli
  • Ospedale SS Annunziata

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Intervention

Control

Arm Description

Clinicians allocated to intervention arm will receive an e-learning educational program based on simulation-based technologies (Dr Sim). Dr Sim provides a powerful editing system that allows to create clinical cases according to the educational need and purposes. It will be distributed on an e-learning platform, allowing the user to act in a highly interactive learning environment. Management of the virtual patients is carried out interactively and each diagnostic and or therapeutic choice will be supported by any scientific data, guidelines recommendations, drug descriptions and literature references useful to address the best choice for that specific patient as it should be in real practice.

Clinicians allocated to control arm will not receive the e-learning educational program based on simulation-based technologies (Dr Sim).

Outcomes

Primary Outcome Measures

Elderly with AF prescribed with OAC
difference in the proportion of elderly patients with AF prescribed with OAC between the post-intervention and the pre-intervention observational phase

Secondary Outcome Measures

Number of access to Dr Sim
average number of access to Dr. Sim among the phsyicians of the centres randomised to the intervention during the 1 month intervention phase
Total duration of connection to Dr Sim
average total duration of connection to Dr. Sim among the phsyicians of the centres randomised to the intervention during the 1 month intervention phase
Elderly patients with AF prescribed with any antiplatelet agent
difference in the proportion of elderly patients with AF prescribed with any antiplatelet agent (and not OAC) between the post-intervention and the pre-intervention observational phase
Elderly patients with AF newly prescribed with OAC agents
difference in the proportion of elderly patients with AF prescribed with new OAC agents between the post-intervention and the pre-intervention observational phase
Patients experiencing any cerebro or cardiovascular events
proportion of patients experiencing any stroke, transient ischaemic attack (TIA), other major arterial or venous thromboembolism during the 6 months after the hospital discharge
Re-hospitalization rate
proportion of patients re-hospitalised for any cause during the 6 months after the hospital discharge
Minor bleeding events
proportion of patients experiencing a minor bleeding event during the 6 months after hospital discharge)
Major bleeding event
proportion of patients experiencing a major bleeding event during the 6 months after hospital discharge)

Full Information

First Posted
June 5, 2017
Last Updated
November 8, 2018
Sponsor
Mario Negri Institute for Pharmacological Research
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1. Study Identification

Unique Protocol Identification Number
NCT03188211
Brief Title
E-learning to Improve Oral Anticoagulant Use in Hospitalized Older People With AF
Acronym
SIM-AF
Official Title
Simulation-based Technologies to Improve the Appropriate Use of Oral Anticoagulants in Hospitalized Elderly Patients With Atrial Fibrillation
Study Type
Interventional

2. Study Status

Record Verification Date
November 2018
Overall Recruitment Status
Completed
Study Start Date
September 1, 2017 (Actual)
Primary Completion Date
January 22, 2018 (Actual)
Study Completion Date
September 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mario Negri Institute for Pharmacological Research

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
Atrial Fibrillation (AF) is the most common cardiac arrhythmia and the main cause of cardioembolic stroke. Oral Anticoagulation (OAC) has been shown to significantly prevent AF-related thromboembolism, however, despite convincing evidences and current guidelines recommendations, OAC tends to be underused in clinical practice especially in the oldest. Education and training to appropriately select people suitable for OAC for stroke prevention could be pivotal in the decision making process. According to the study project, physicians working in Internal Medicine and Geriatric wards, where are mainly admitted elderly people with AF, will undergo to a program of e-learning through computer-based simulation method reproducing clinical scenarios of patients aged 65 years or older, with known or newly diagnosed AF, admitted to hospital for any medical reason and requesting that a decision about long-term antithrombotic therapy is taken. Primary objective of the study is to investigate whether such educational intervention will improve the appropriate use and prescription rate of OAC in hospitalised elderly patients with AF, multimorbidity and polypharmacy, in comparison to the usual practice. The study will be a cluster randomised controlled trial involving a network of Internal Medicine and Geriatrics wards. Thirty-two wards will be recruited based on voluntary participation and randomised to receive an educational intervention through computer-based simulation, (N=16) or to continue with the usual practice (N=16). Subjects receiving the intervention will be all the staff physicians of the wards randomised in the intervention arm. The impact of the intervention compared with the usual practice will be evaluated in patients aged 65 years or older admitted to the participating centres with a known diagnosis of AF or newly diagnosed with AF during the hospitalisation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Simulation Training, Anticoagulant Drugs, Elderly, Atrial Fibrillation, Drug Prescriptions, Internal Medicine, Geriatrics

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
cluster randomized controlled trial
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
247 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Other
Arm Description
Clinicians allocated to intervention arm will receive an e-learning educational program based on simulation-based technologies (Dr Sim). Dr Sim provides a powerful editing system that allows to create clinical cases according to the educational need and purposes. It will be distributed on an e-learning platform, allowing the user to act in a highly interactive learning environment. Management of the virtual patients is carried out interactively and each diagnostic and or therapeutic choice will be supported by any scientific data, guidelines recommendations, drug descriptions and literature references useful to address the best choice for that specific patient as it should be in real practice.
Arm Title
Control
Arm Type
Other
Arm Description
Clinicians allocated to control arm will not receive the e-learning educational program based on simulation-based technologies (Dr Sim).
Intervention Type
Other
Intervention Name(s)
E-learning educational program
Other Intervention Name(s)
Dr Sim
Intervention Description
A number of 10 cases of patients 65 years of age or older with AF, acutely admitted to Internal Medicine or Geriatric wards for any medical condition, will be edited into the Dr. Sim system. Diagnostic and therapeutic choices for ordinary and/or complex medical situations will be taken through the development of the simulated scenario.
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
Any educational program will be delivered to clinicians assigned to control arm
Primary Outcome Measure Information:
Title
Elderly with AF prescribed with OAC
Description
difference in the proportion of elderly patients with AF prescribed with OAC between the post-intervention and the pre-intervention observational phase
Time Frame
through study completion, up to 1 year
Secondary Outcome Measure Information:
Title
Number of access to Dr Sim
Description
average number of access to Dr. Sim among the phsyicians of the centres randomised to the intervention during the 1 month intervention phase
Time Frame
1 month
Title
Total duration of connection to Dr Sim
Description
average total duration of connection to Dr. Sim among the phsyicians of the centres randomised to the intervention during the 1 month intervention phase
Time Frame
1 month
Title
Elderly patients with AF prescribed with any antiplatelet agent
Description
difference in the proportion of elderly patients with AF prescribed with any antiplatelet agent (and not OAC) between the post-intervention and the pre-intervention observational phase
Time Frame
through study completion, up to 1 year
Title
Elderly patients with AF newly prescribed with OAC agents
Description
difference in the proportion of elderly patients with AF prescribed with new OAC agents between the post-intervention and the pre-intervention observational phase
Time Frame
through study completion, up to 1 year
Title
Patients experiencing any cerebro or cardiovascular events
Description
proportion of patients experiencing any stroke, transient ischaemic attack (TIA), other major arterial or venous thromboembolism during the 6 months after the hospital discharge
Time Frame
6 month follow up
Title
Re-hospitalization rate
Description
proportion of patients re-hospitalised for any cause during the 6 months after the hospital discharge
Time Frame
6 month follow up
Title
Minor bleeding events
Description
proportion of patients experiencing a minor bleeding event during the 6 months after hospital discharge)
Time Frame
6 month follow up
Title
Major bleeding event
Description
proportion of patients experiencing a major bleeding event during the 6 months after hospital discharge)
Time Frame
6 month follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: subjects 65 years of age or older, with known or newly diagnosed AF, admitted to the Internal Medicine and Geriatric wards of the REPOSI network, consent to participate to the study. Exclusion Criteria: consent denial to participate to the study, absolute contraindication to OAC, re-hospitalisation for the subject already included in the study, life expectancy less than 6 months.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paola Santalucia, MD
Organizational Affiliation
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico di Milano
Official's Role
Principal Investigator
Facility Information:
Facility Name
Azienda Ospedaliera Universitaria Policlinico Sant'Orsola Malpighi
City
Bologna
State/Province
Bo
ZIP/Postal Code
40138
Country
Italy
Facility Name
Istituto Fondazione Poliambulanza
City
Brescia
State/Province
BS
ZIP/Postal Code
25100
Country
Italy
Facility Name
Policlinico Universitario Mater Domini
City
Catanzaro
State/Province
CZ
ZIP/Postal Code
88100
Country
Italy
Facility Name
AO Universitaria Policlinico di Modena
City
Modena
State/Province
Italia
ZIP/Postal Code
41124
Country
Italy
Facility Name
Azienda Ospedaliera S. Gerardo di Monza
City
Monza
State/Province
MB
ZIP/Postal Code
20900
Country
Italy
Facility Name
Ospedale degli Infermi
City
Rivoli
State/Province
TO
ZIP/Postal Code
10098
Country
Italy
Facility Name
Azienda Ospedaliera Universitaria - Ospedale Riuniti
City
Trieste
State/Province
TS
ZIP/Postal Code
34121
Country
Italy
Facility Name
A.O. Ospedale di Circolo e Fondazione Macchi
City
Varese
State/Province
VA
ZIP/Postal Code
21100
Country
Italy
Facility Name
Azienda Consorziale Ospedaliera Policlinico
City
Bari
Country
Italy
Facility Name
Azienda Ospedaliera Papa Giovanni XXIII
City
Bergamo
ZIP/Postal Code
24127
Country
Italy
Facility Name
Azienda Ospedaliera Universitaria "Policlinico Vittorio Emanuele"
City
Catania
Country
Italy
Facility Name
Azienda Ospedaliera Universitaria San Martino - IST
City
Genoa
Country
Italy
Facility Name
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
City
Milano
Country
Italy
Facility Name
Azienda Ospedaliera di Padova
City
Padova
ZIP/Postal Code
35128
Country
Italy
Facility Name
Azienda Ospedaliera Universitaria Policlinico P. Giaccone
City
Palermo
Country
Italy
Facility Name
Azienda SocioSanitaria Territoriale, Ospedale Civile "C.Mira" di Casorate Primo
City
Pavia
Country
Italy
Facility Name
Policlinico San Matteo
City
Pavia
Country
Italy
Facility Name
Ospedale San Giovanni Calibita Fatebenefratelli
City
Roma
Country
Italy
Facility Name
Policlinco Universitario Agostino Gemelli
City
Rome
Country
Italy
Facility Name
Ospedale SS Annunziata
City
Sassari
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29657108
Citation
Proietti M, Antoniazzi S, Monzani V, Santalucia P, Franchi C; SIM-AF Investigators; Fenoglio LM, Melchio R, Fabris F, Sartori MT, Manfredini R, De Giorgi A, Fabbian F, Biolo G, Zanetti M, Altamura N, Sabba C, Suppressa P, Bandiera F, Usai C, Murialdo G, Fezza F, Marra A, Castelli F, Cattaneo F, Beccati V, di Minno G, Tufano A, Contaldi P, Lupattelli G, Bianconi V, Cappellini D, Hu C, Minonzio F, Fargion S, Burdick L, Francione P, Peyvandi F, Rossio R, Colombo G, Monzani V, Ceriani G, Lucchi T, Brignolo B, Manfellotto D, Caridi I, Corazza GR, Miceli E, Padula D, Fraternale G, Guasti L, Squizzato A, Maresca A, Liberato NL, Tognin T, Rozzini R, Bellucci FB, Muscaritoli M, Molfino A, Petrillo E, Dore M, Mete F, Gino M, Franceschi F, Gabrielli M, Perticone F, Perticone M, Bertolotti M, Mussi C, Borghi C, Strocchi E, Durazzo M, Fornengo P, Dallegri F, Ottonello LC, Salam K, Caserza L, Barbagallo M, Di Bella G, Annoni G, Bruni AA, Odetti P, Nencioni A, Monacelli F, Napolitano A, Brucato A, Valenti A, Castellino P, Zanoli L, Mazzeo M. Use of oral anticoagulant drugs in older patients with atrial fibrillation in internal medicine wards. Eur J Intern Med. 2018 Jun;52:e12-e14. doi: 10.1016/j.ejim.2018.04.006. Epub 2018 Apr 12. No abstract available.
Results Reference
result
PubMed Identifier
31218738
Citation
Antoniazzi S, Ardoino I, Proietti M, Monzani V, Mannucci PM, Nobili A, Franchi C; SIM-AF Collaborators. Appropriateness of prescription of oral anticoagulant therapy in acutely hospitalized older people with atrial fibrillation. Secondary analysis of the SIM-AF cluster randomized clinical trial. Br J Clin Pharmacol. 2019 Sep;85(9):2134-2142. doi: 10.1111/bcp.14029. Epub 2019 Jul 19.
Results Reference
derived
PubMed Identifier
31075225
Citation
Franchi C, Antoniazzi S, Ardoino I, Proietti M, Marcucci M, Santalucia P, Monzani V, Mannucci PM, Nobili A; SIM-AF Collaborators. Simulation-Based Education for Physicians to Increase Oral Anticoagulants in Hospitalized Elderly Patients with Atrial Fibrillation. Am J Med. 2019 Aug;132(8):e634-e647. doi: 10.1016/j.amjmed.2019.03.052. Epub 2019 May 8.
Results Reference
derived
Links:
URL
http://www.ncbi.nlm.nih.gov/pubmed/29657108
Description
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E-learning to Improve Oral Anticoagulant Use in Hospitalized Older People With AF

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