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| ID | Type | Description | Link |
|---|---|---|---|
| 2016- A01086-45 | Other Identifier | ANSM |
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Logistical issues
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Poor physical performance and poor nutritional status increase the risk of complications after major surgery. Prehabilitation is the process of enhancing the functional capacity before surgery.
A major problem is the adherence of the patients to the physical program. A controlled randomized study is therefore proposed to determine the impact of coaching on functional exercise capacity. All patients will wear connected devices to measure their physical activity. They will be randomized to either a group in which coaching will be adapted to the physical activity, or a control group in which coaching is performed without any information about physical activity
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Connected device with close following | Experimental | Data from connected devices (arm wrist watch, connected monitor of blood pressure, connected thermometer and pulse oximeter) will be analyzed every day and used for coaching |
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| Connected device with standard coaching | Other | Data from connected devices (arm wrist watch, connected monitor of blood pressure, connected thermometer and pulse oximeter) will be saved but not used for coaching |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Optimized group | Device | The data provided by the connected devices is analyzed daily; the patient receives a phone call in case of no realization of the objectives. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Functional capacity | 6 minutes walk test | 2 months |
| Functional capacity | Maximal oxygen consumption | 2 months |
| Measure | Description | Time Frame |
|---|---|---|
| Critical events | Number of critical events detected using the connected devices | 2 months |
| Postoperative complications | Number of complication during the 2 months following surgery according to Dindo and Clavien classification |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Barizien Nicolas, MD | Hopital Foch | Principal Investigator |
| Marc Fischler | Hopital Foch | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Foch hospital | Suresnes | France |
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| ID | Term |
|---|---|
| D035061 | Control Groups |
| ID | Term |
|---|---|
| D015340 | Epidemiologic Research Design |
| D004812 | Epidemiologic Methods |
| D008919 | Investigative Techniques |
| D012107 | Research Design |
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| Control group | Device | Data will be recorded but not analyzed daily during the period of participation. The patient receives a phone call one time a week to answer possible questions and modify the prescription of physical activity if need. |
|
| 2 months |
| D008722 | Methods |