From: Harnessing the potential of community-based participatory research approaches in bipolar disorder
Concern | Potential solutions |
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Some types of conclusions and statements may be distressing for those with lived experience | Consider in advance how to include information about protective factors in research designs; consider language in describing findings carefully; give advance warning to consumers about findings that might be on difficult topics, allowing choice about participation; consider whether findings are being presented in the most compassionate manner; plan for ongoing supervision to review and support individual’s response to difficult material |
Those with BD may go through symptomatic periods that interfere with productivity | Plan in advance for back-up and recovery time; consider working with teams of individuals rather than relying on a single person |
Symptoms may emerge in a way that interfere with privacy or work flow | Develop an understanding in advance of how symptoms will be discussed and managed if they are apparent in the workplace |
Some with lived experience may have less scientific background than other team members | Invest in training team members to understand the research process Develop an understanding of key and valued roles that can be well-managed by those with less scientific background |
Some with lived experience may have government benefits that be will be jeopardized if they work more than a certain number of hours, and others may prefer to maintain flexible hours | Discuss levels of commitment and constancy in advance, and use this knowledge to plan work roles that will not suffer from part-time or varied time involvement |
Organizations may not value lived experience as well as they do scientific experience, leading to the potential for inequality in promotions and career advancement over time | Team leaders need to work at a systematic level to change organizational barriers |