Main reason for conducting a pilot study | Feasibility objective | Feasibility questions | Programme level | Criterion for feasibility success |
---|---|---|---|---|
Resources | Efforts for and completeness of recording data | Are the efforts for the participation in the trial reasonable? Is enough data obtained for a reasonable decision-making? Are the expenses justifiable? | residents | Less than 50% the residents would not participate again in the trial or drop out during the trial (RES_1) |
 |  |  | nurses | Less than 50% the nurses would not participate again in the trial or drop out during the trial (RES_2) |
 |  |  | both | Percentage of missing values below 20% for SOPMAS, below 50% for MOTPA (RES_3) |
Scientific | Minimum effects (justifying further research) | Is Kinaesthetics mobilisation able to increase safety, participation and comfort as well as decrease pain for the residents? | residents | After staff training, at least 50% of the residents (a) perceive more safety, comfort and participation during mobilisation (at least 2 points, SCI_1) (b) perceive less pain during mobilisation (at least 2 points) SCI_2 (c) receive a higher median SOPMAS score of item "patient movement" (at least 1 point) (SCI_3) |
 |  | Is Kinaesthetics mobilisation able to decrease perceived physical strain and increase movement competence of the nurses ? | nurses | After staff training, at least 50% of the nurses (a) perceive less physical strain during mobilisation (at least 2 points) or increased Borg values can be ascribed to improvements in body perception (SCI_4) (b) receive a higher median SOPMAS score (at least 1 point) (SCI_5) |
Process | Continuing Participation | Will residents and nurses be ready to participate in the trial over the full period? | residents | 50% or less of the residents leave the programme on their own decision (i.e. not due to an adverse event or death (PRO_1) |
 |  |  | nurses | 30% or less of the nurses leave the programme on their own decision (i.e. not due to an adverse event, PRO_2) |