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Report from Second Year Special Interest Group Meeting on Promoting Partnerships Between Researchers

IMFAR Special Interest Group, 2018

Rotterdam, The Netherlands

May 12, 2018

Summary: On May 12, 2018, the Special Interest Group at the International Society of Autism Research entitled “Promoting Partnerships Between Researchers and Patient Advocacy Organizations” met from 7:15AM – 8:45AM. This year’s INSAR meeting was held in Rotterdam, Netherlands, and approximately 50 people were in attendance at this year’s SIG. Three presentations were made and the powerpoint slides can be found here. The group continued discussion on the importance of patient registries in research with some examples of actions that have been taken since last year’s SIG to advance coordination of existing registries. In addition, a presentation was made about different ways to engage the community on the diagnostic journey as well as about autism research in general. The group then broke out into different groups to tackle the following questions. General needs as well as potential action items are listed at the bottom.

Research Questions


  • What would a registry which included information from multiple “forms” of autism add? How could it be used?

  • What would be the most pressing research questions to answer? (from researchers and stakeholders)

  • How could or should patient advocacy organizations be involved?

  • What data is not being collected that you think should be?

Communicating with families:

  • How do researchers typically communicate science to families?

  • Why do they discuss the findings with families?

  • Who makes decisions about what to share, and how, and how often, etc.?

  • From a stakeholder perspective, how is scientific information delivered from researchers used?

  • What resources do researchers wish they had but don’t have? This includes from first point of contact to years and years beyond.

  • FOLLOW UP: What do researchers need from patient advocacy organizations and places like ASF and AS in getting the message to families?

Shafali Jeste, PhD, of UCLA

Shafali Jeste, PhD, of UCLA​

Summary of Discussions



  • Getting families engaged in registries

  • Flexible tiers of registries, with a basic entry-point that is common to all registries, then more specific questions based on genetic syndrome

  • Gaps in communicating with families about registries


  • Short term: complete common data elements, 1 page marketing piece value of registries for families and distributing to PAGs, 1 pager value of research and clinical trials in general for clinicians and families, document for researchers on value of registries

  • Long term: single portal, toolkit for new groups, they will have a compatible system