Prospective, non-randomized, open-label, pilot study conducted in a single group of 30 evaluable patients, i.e. patients completing an approximate 3 month follow-up.
The eHealth system developed in the present study is dedicated to multimorbid patients' follow-up. The medical device consists in Telemonitoring, Telenotification and Telecoaching. It aims to both increase patient autonomy, with regard to management of his/her pathologies, and facilitate coordination between health professionals. By providing patients with tools enabling early detection of clinical worsening combined with an appropriate management, the medium and long-term objectives are to reduce hospitalizations and improve health status and quality of life of these patients at home. In the first instance, the only objective of the present study is to evaluate the performance and feasibility of implementation of the device. This evaluation is based on a comparison between the telenotifications generated by the software and those calculated from the raw data captured by the software.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
23
Cabinet Privé de Cardiologie - 2, rue jean jaurès
Annecy, France
Cabinet Privé de Pneumologie - 7 rue gabriel de mortillet
Annecy, France
Centre Hospitalier d'Annecy Genevois - service cardiologie - 1 avenue de l'Hôpital BP 90074 Metz-Tessy
Pringy, France
Centre Hospitalier d'Annecy Genevois - service pneumologie - 1 avenue de l'Hôpital BP 90074 Metz-Tessy
Sensitivity and specificity of the tele-notifications
Time frame: through study completion, an average of 11 months
Sensitivity and specificity of the STABILITY SYSTEM INDICATORS
Time frame: through study completion, an average of 11 months
Specific self-administered questionnaires about Ease of Use/Usefulness/Satisfaction for each category of user
Time frame: through study completion, an average of 11 months
Acceptability of the system by patients regarding transmission of measured parameters
Mean number of transmission of measured parameters: real versus theoretical.
Time frame: through study completion, an average of 11 months
Acceptability of the system by patients: mean number of participation in virtual classroom session
Time frame: through study completion, an average of 11 months
Acceptability of the system by patients: mean duration of participation in virtual classroom session
Time frame: through study completion, an average of 11 months
Acceptability of the system by patients: mean number of consultations of modules providing medical information
Time frame: through study completion, an average of 11 months
Acceptability of the system by patients: cumulative time spent on consultations of modules providing medical information
Time frame: through study completion, an average of 11 months
Acceptability of the system by patients: mean duration of phone contacts by type (planned, for notification management, incoming)
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Pringy, France
Cabinet privé de pneumologie - 28 avenue de Genève
Saint-Julien-en-Genevois, France
cabinet privé de médecine générale - 18, rue Louis Haase
Thônes, France
Time frame: through study completion, an average of 11 months
Acceptability of the system by patients: mean number of phone contacts by type (planned, for notification management, incoming)
Time frame: through study completion, an average of 11 months
Acceptability of the system by patients: comparison of real planned phone contacts versus theoretical
Time frame: through study completion, an average of 11 months
Acceptability of the system by physicians: mean number of connections
Time frame: through study completion, an average of 11 months
Acceptability of the system by physicians: mean duration of connections
Time frame: through study completion, an average of 11 months
Feasibility of the intervention for patients
number of screening failure and prematurely withdrawal
Time frame: through study completion, an average of 11 months
Feasibility of the intervention for technicians
duration of intervention
Time frame: through study completion, an average of 11 months
Feasibility of the intervention for nurses
response time following a notification
Time frame: through study completion, an average of 11 months
Technological performance indices of the system: failures in data transmission
Time frame: through study completion, an average of 11 months
Technological performance indices of the system: inaccessibility
Time frame: through study completion, an average of 11 months
Technological performance indices of the system: devices deficiencies
technical problems with any medical devices (leading or not to replacement).
Time frame: through study completion, an average of 11 months
Number of tele-notification per patient
Time frame: through study completion, an average of 11 months
Frequency of tele-notifications per patient
Time frame: through study completion, an average of 11 months
Patient care plan: number of changes implemented by investigators.
Time frame: through study completion, an average of 11 months
Clinical events including medical consultations, hospitalizations and adverse events
Overall description of medical consultations, hospitalizations and adverse events. For adverse events, in addition, evaluation of seriousness and causal relationship with the medical device of the study.
Time frame: through study completion, an average of 11 months