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Clinical Trial Summary

Nearly half of the U.S. population sometimes or always experiences loneliness, which is alarming given that loneliness confers risk for negative mental and physical health outcomes. Extensive research suggests loneliness is characterized by subjective isolation: many lonely individuals maintain a number of relationships but still report feeling lonely. The goal of this proposal is to use functional magnetic resonance imaging to reveal how the brain represents our subjective connection to and isolation from other people, which will ultimately inform optimal ways to intervene to reduce loneliness.


Clinical Trial Description

Extensive research suggests loneliness is characterized by subjective isolation: many lonely individuals maintain a number of relationships but still report feeling lonely. Thus, a neurobiological account of loneliness requires that we understand how the brain represents our subjective connections to others and how loneliness alters these representations. The long-term goal of this proposal is to identify how subjective isolation is represented in the brain in order to identify novel ways to intervene on this representation to attenuate loneliness. We propose that the brain organizes our representations of people based on our subjective connection to them and that loneliness systematically alters this organization. In Specific Aim 1, we will determine whether subjective closeness organizes self and other representations in the brain. While undergoing fMRI, participants will complete tasks in which they reflect on themselves and other people. They will also report on their subjective closeness to the other people. We will test whether the brain organizes mental representations of the self and one's own social network members based on subjective closeness. In Specific Aim 2, we will determine how loneliness modulates self and other representations in the brain. In Specific, Exploratory Aim 3, we will determine the cognitive consequences of altered self and other representation in loneliness. Our proposal is imperative for ultimately revealing neurocognitive mechanisms to intervene on to reduce loneliness. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04577911
Study type Observational
Source Trustees of Dartmouth College
Contact Meghan L Meyer, PhD
Phone 16505211701
Email meghan.l.meyer@dartmouth.edu
Status Recruiting
Phase
Start date April 1, 2021
Completion date July 1, 2025

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