Knowledge Translation Gaps that Need to be Bridged to Enhance Life for People with Spinal Cord Injury

Abstract

There is a ‘need to know’ for people who have acquired a spinal cord injury (SCI)1 and a ‘lack of knowledge’ is considered to be a barrier to coping with SCI 2. In-patient SCI care and rehabilitation have emphasized that information should be provided in the right amounts, at the right place and at the right time 3. Such needs and timing probably go beyond initial care and rehabilitation. Likewise, there is also, reasonably a need for knowledge for other groups of people meeting people with SCI,4,5 such as relatives, health professionals and personal care assistants as well as authorities, decision-makers, employers, architects and city planners etc. Our recent work,7 shows that more evidence is needed regarding the provision of specialist expertise in SCI by care services and to what extent they are therefore able to respond to the needs of people living with SCI.A Swedish need assessment project, including a priority setting partnership (PSP ) according to James Lind Alliance,8 has been implemented nationwide 2021–22 to address the needs which are most important for people with SCI to enhance their lives. The Swedish need assessment project comprises three parts: (a) needs to be met; (b) questions to be answered; (c) knowledge required. In part (b), which is the PSP we have identified research priorities7 (e.g. knowledge gaps); while in part (c), presented here, we report results from an online survey addressing knowledge translation gaps in order to shed light on the knowledge that is available yet which does not reach out.