Table 2. Data-sharing statement details on trials registrations.
Non-commercial funded RCTs N = 100 | Non-commercial funded RCTs N = 100 | |
---|---|---|
Data sharing plan in the registration? | 77 [67% - 85%] | 81 [72% - 88%] |
Intention to share IPD | ||
Yes | 12 [7% - 20%] | 59 [49%– 69%] |
Undecided | 12 [7%– 20%] | 9 [4%– 17%] |
No | 54 [44%– 64%] | 16 [10%– 25%] |
Nothing specified | 22 [15%– 32%] | 16 [10%– 25%] |
Information about supporting material availability? | 12 [7%– 20%] | 37 [28%– 47%] |
Information about protocol availability? | 11 [6%– 19%] | 33 [25%– 44%] |
Information about SAP availability? | 9 [4%– 17%] | 32 [23%– 42%] |
Information about CSR availability? | 6 [2%– 13%] | 33 [24%– 43%] |
Mention of timeframe of data availability? | 11 [6%– 19%] | 19 [12%– 28%] |
Data will be freely accessible? | 6 [2%– 13%] | 26 [18%– 36%] |
Mention of restriction of data access? | 1 [0.5%– 6%] | 12 [7%– 20%] |
Mention of a specific aim for data reuse? | 3 [0.7%– 9%] | 6 [2%– 13%] |
Mention of data access methods? | 6 [2%– 13%] | 47 [37%– 57%] |
Data are presented as percentages and their corresponding 95% confidence intervals.