In addition, client 1 needed only 60% of the transmission completion time to complete the experiment in scenario 2, in which data were obtained from the cloudlets that coordinated with each other instead of from the cloudlets that were directly connected with the remote cloud.
The performance of all three clients improved in scenario 1, and this improvement was even greater in scenario 2. For instance, Fig. 11 shows that client 1 needed approximately 85% of the transmission completion time to complete the experiment in scenario 1, in which data were obtained from the cloudlet instead of directly from the remote cloud.
This analysis is aimed specifically at how the benefit to completion, the intention to complete, student satisfaction, several demographic and educational variables, and actual completion are related.
Participants who were adolescents when they assented to participation in PING, but then turned 18 prior to PhenX completion, were asked to complete an additional adult consent form.
Follow-up MacTSQ data were collected at 12 months, by which time 110 of the 137 participants remained in the trial (deceased = 5, exited study prior to second MacTSQ completion = 6, unable to complete within the required time for second completion of MacTSQ = 6, unknown reason for leaving study = 10).
The analysis also revealed a somewhat weaker relationship between completion and the intention to complete, qualification level, student age, and several interactions between these variables.
Upon completion, students were asked to complete an encounter note.
Between registration and study completion, parents were asked to complete weekly sleep diaries.
After task completion, participants were asked to complete a taste test (based on Houben, 2011) and the same filler questionnaires as in Experiment 1.
There were very low rates (<2%) of partial completion (defined as failure to complete at least one item) across measures and follow-up points, with individuals tending to either complete the whole measure or not respond at all.
From these, 91 completed the trial, with five being discharged before completion, two not willing to complete and two being excluded due to discomfort with ingestion of thin liquid.
