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Building Consensus

Despite growing recognition of loneliness and isolation as urgent public health challenges, the field faces a critical barrier: the lack of alignment and consistency in how we measure social isolation, loneliness, and social connection (SILC). Current tools are fragmented, outdated, and often fail to reflect lived experiences, hindering the evaluation of interventions and the advancement of patient-centered comparative clinical effectiveness research (CER).

To address this challenge, the Foundation for Social Connection convened leading researchers, clinicians, patients, and other advocates at Building Consensus on March 23-24 in Washington, D.C. Together, we assessed current tools, learned from patient perspectives, and built consensus on validated approaches that strengthen research and improve patient-centered care.

Agenda

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Connect with Others

Explore who joined us below! To help spark new connections and collaborations, we’re sharing an attendee list so participants can see who’s in the room, identify shared interests, and build relationships.

Our Oversight Committee

The convening was guided by an Oversight Committee composed of leading researchers and stakeholders with expertise in patient-centered comparative effectiveness research (CER). The Committee provided strategic input on planning, patient and stakeholder engagement, and alignment with existing measurement efforts, helping ensure the convening reflected rigorous science, equity, and real-world relevance for aging and health research.

SPARKS Program


As part of this convening, we created the SPARKS (Scholars on the Path to Advance Research and Knowledge on Social connection) Program to support promising early-stage investigators committed to advancing research on social connection, loneliness, and social isolation. The program provides travel support, mentorship from established scholars, and dedicated networking and training opportunities to help cultivate the next generation of researchers in patient-centered comparative effectiveness research. Below are our SPARKS mentors and mentees.

Sponsored By

The Patient-Centered Outcomes Research Institute (PCORI) is an independent nonprofit organization authorized by Congress in 2010. Its mission is to fund research that will provide patients, their caregivers and clinicians with the evidence-based information needed to make better-informed health care decisions. PCORI is committed to continuously seeking input from a broad range of stakeholders to guide its work.

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