Table 4.
Basic usage statistics: |
•All patients used the system. |
•The average number of sessions per patient was 27 (SD 18, range 4–69) in the six weeks study period. |
•On average, a patient-session lasted 12 minutes. The longest patient-session lasted 1 hour and 38 minutes. |
•Of all patient-sessions, 16 percent took place after office hours (between 19:00 and 07:00 next day). |
•On average, each patient completed 12.6 monitoring questionnaires. |
•21 patients sent, on average 4.5 messages. Half of these messages contained a question, and half were personal reports on how the patient was doing. |
Summary of other findings: |
•Using the system, in eight patients potential problems requiring direct medical actions were detected. |
•56% of the patients had no experience with computers before participation. |
•Overall appreciation score for “the system as a whole” was 8.0 on a 10 point scale. |
•86% of patients felt that health care providers could keep a better eye on their illness, and 83% felt that the system provided a feeling of security. |
•89% of patients would advise other patients in similar situations to use the system as well. |
∗ Described in more detail in: van den Brink et al. Involving the patient: a prospective study on use, appreciation and effectiveness of an information system in head and neck cancer care. Int J Med Inform. 2005 Oct;74(10):839–49.