NEUTROSIS: Shared Health Information System for Febrile Neutropenia
Study Details
Study Description
Brief Summary
The use of e-health in improving the quality of health services is a rapidly expanding research area, in particular its usefulness in patient management of the home-hospital care pathway. Febrile neutropenia is a serious and frequent complication of cytotoxic chemotherapy and better identification of low-risk patients who can be treated at home could be made possible by these technologies.
The objective of this study is to evaluate a shared health information system (NEUTROSIS) for home-hospital management of febrile neutropenia after anti-tumor chemotherapy. The study aims to compare the average length of hospital stay for febrile neutropenia among patients receiving NEUTROSIS and those receiving standard care
Materials and methods A shared information system (NEUTROSIS) has been developed to connect a smartphone web application for the patient to the existing shared medical record of the Paris Sud hospital group (AP-HP, France - 4D software).
The study consists of conducting a randomized controlled trial to compare a cohort of patients receiving cytotoxic chemotherapy for solid cancer or heamatological malignancies using the NEUTROSIS shared information system (n=100) and a cohort of patients followed by the hospital's standard care over a treatment period of six months (n=100). During the 15 days following each chemotherapy cycle, the 2 groups of patients must take their temperature daily. Both groups are trained like any patient under chemotherapy to contact the team in case of fever. The NEUTROSIS group captures daily its temperature and the occurrence of other symptoms on the smartphone application. This information is then transmitted instantly to the hospital care team who will be alerted in case of fever and will contact the patient. The control group will indicate these same data in a paper diary and will have to contact the health team in case of fever as done in the usual care.
The two groups of patients will be followed 6 months through a questionnaire asked to the patient at each hospital visit for chemotherapy cycle. The questionnaire collects information on the occurrence of symptoms and healthcare use between two chemotherapy cycles. A last follow-up questionnaire is asked by phone at the endpoint follow-up (6 months). The study will take place in two hospital sites of the Paris University hospital (A Béclère and Kremlin-Bicètre).
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: NEUTROSIS Intervention Group The NEUTROSIS Intervention group captures daily its temperature and the occurrence of other symptoms on the smartphone application. This information is then transmitted instantly to the hospital care team through the NEUTROSIS shared information system. The medical oncologist will be alerted in case of fever and will contact the patient. |
Device: NEUTROSIS
evaluate a shared health information system (NEUTROSIS) for home-hospital management of febrile neutropenia after anti-tumor chemotherapy
|
| No Intervention: CONTROL Group The control group will monitor daily its temperature and the occurrence of other symptoms on a paper surveillance diary and will have to contact the health team in case of fever as done in the usual care. |
Outcome Measures
Primary Outcome Measures
- average length of hospital stay for febrile neutropenia [6 months]
average length of hospital stay for febrile neutropenia
Secondary Outcome Measures
- hospitalisation rate [6 months]
hospitalisation rate
- healthcare use rate [6 months]
emergency department, general practitioner,
- Use rate [6 months]
patient use rate
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Age> 18 years
-
Patient receiving cytotoxic chemotherapy for solid tumor or hematological malignancy
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Patient having signed consent to participate in the study
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Patient able to understand the protocol of care
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Patient covered by health insurance
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Patient with the use of a smartphone or tablet with Internet connection
Exclusion Criteria:
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patient refusing to participate in the study
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patient participating in a drug trial
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patient receiving or shifting to a weekly chemotherapy protocol
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Hôpital Antoine Béclère | Clamart | France | 92140 | |
| 2 | Hôpital d'instruction des Armées de Percy | Clamart | France | 92140 | |
| 3 | Hôpital BICETRE | Le Kremlin-Bicêtre | France | 94275 |
Sponsors and Collaborators
- Marie-Helene METZGER
- Assistance Publique - Hôpitaux de Paris
- Institut National de la Santé Et de la Recherche Médicale, France
Investigators
- Principal Investigator: Francois BOUE, MD,PhD, Assistance Publique - Hôpitaux de Paris
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 16-009