Table 2.
Sub-step | Description | |
---|---|---|
3a | Determine requirements of the PROM | Requirements may include the type of PROM (e.g. generic of specific), mode of administration (e.g. paper/pencil, web-based), measurement properties (see also 3d), applicability (see also step 3e). |
3b | Identify potential PROMs | Identification of PROMs per selected PRO through a systematic search of the literature and existing databases. |
3c | Initial selection of potential PROMs | Initial selection through content validity by evaluating the relevance, comprehensiveness, and comprehensibility of the items and domains of the PROM – does the PROM measure the selected PROs? |
3d | Determine measurement properties of the PROM | Evaluate the reliability, validity and responsiveness of the potential PROMs. The COSMIN methodology may assist in the evaluation. |
3e | Determine feasibility, interpretability and acceptability of the PROM | Feasibility is related to various aspects such as the time of administration (number of items), availability of translated version, and costs for using the PROM; interpretability is related to meaningful use of the scores on the PROM such as minimal clinical important difference; acceptability is related to support of patients and clinicians in using the PROM |
3f | Select suitable PROM(s) | Selection of the PROM(s) based on the outcomes of step 3d and 3e, for which formal and informal consensus procedures can be used. |
3g | Determine the next step | The next step could be testing of the selected PROM (step 4 in the PROM-cycle), adaptation of an existing PROM through further development and testing; or development of a new PROM if no existing PROMs meet the requirements. |
PRO Patient Reported Outcome, PROM Patient Reported Outcome Measure, COSMIN COnsensus-based Standards for the selection of health Measurement Instruments [9]