Table 2 Participants’ responses regarding their expectations of users’ autonomy before using the system
From: Data management system for diabetes clinical trials: a pre-post evaluation study
Users’ autonomy | Strongly disagree Fr (%) | Disagree Fr (%) | Slightly disagree Fr (%) | Neither Agree nor disagree Fr (%) | Slightly agree Fr (%) | Agree Fr (%) | Strongly Agree Fr (%) | Mean | SD |
|---|---|---|---|---|---|---|---|---|---|
I desire to have control over various dimensions of clinical trial data management. | 15 (50.0%) | 8 (26.6%) | 2 (6.7%) | 5 (16.7%) | 0 | 0 | 0 | 6.1 | 1.12 |
I desire to have control over managing research centers in a clinical trial. | 19 (63.3%) | 6 (20.0%) | 5 (16.7%) | 0 | 0 | 0 | 0 | 6.6 | 0.89 |
I desire to have control over managing all people involved in a clinical trial. | 17 (56.7%) | 6 (20.0%) | 4 (13.3%) | 2 (6.7%) | 1 (3.3%) | 0 | 0 | 6.2 | 1.13 |
I desire to have control over the case report forms of the participants. | 16 (53.3%) | 10 (33.4%) | 2 (6.7%) | 1 (3.3%) | 1 (3.3%) | 0 | 0 | 6.3 | 0.99 |
I desire to have control over the security of clinical trial data. | 13 (43.4%) | 10 (33.4%) | 4 (13.3%) | 1 (3.3%) | 1 (3.3%) | 1 (3.3%) | 0 | 6.0 | 1.23 |
I desire to have control over the quality of clinical trial data. | 19 (63.3%) | 6 (20.0%) | 5 (16.7%) | 0 | 0 | 0 | 0 | 6.6 | 0.89 |
Total mean and SD | 6.3 | 1.05 | |||||||