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Study identifier: NCT07060534 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Building Healthy Eating and Self-Esteem Together for University Students

Condition: Eating Disorders (Excluding Anorexia Nervosa) · Binge-Eating Disorder  ·  Sponsor: University of Kansas

PhaseNA
Planned participants74
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

Eating disorders (EDs) are a critical concern on college campuses. Moreover, since the COVID-19 pandemic, ED prevalence has increased by 62% in university women and 140% in university men. Resources are inadequate to meet demand, leading to delays in students' access to treatment. Untreated (or poorly treated) EDs result in greater healthcare utilization and costs to students, as well as lower academic achievement and increased psychiatric disability and mortality, suggesting a critical need for quality ED treatment on university campuses and to rethink treatment delivery. One way to address this gap in care delivery is to improve treatment accessibility and scalability, such as dissemination via mobile apps. Guided self-help Cognitive Behavior Therapy (CBT-gsh) is a cost-effective option that can be delivered by non-traditional service providers, such as nurses and physicians. Our scientific premise is that the mHealth CBT-gsh app, Building Healthy Eating and Self-Esteem Together for University Students (BEST-U), will lead to reductions in binge eating (primary outcome) through reductions in dietary restraint and weight/shape concerns (target mechanisms). Prior to implementing BEST-U at other universities, we need to test the intervention in a real-world setting with the end goal of disseminating at scale. Our objectives are to: 1) conduct an effectiveness test of BEST-U compared to a similar dose of present-centered therapy (PCT) in students with non-low weight binge-spectr…

This description comes directly from the study's public registry record.

Talk to the study team

Kelsie Forbush, PhD  ·  785-864-6525  ·  kforbush@ku.edu

Kara Christensen-Pacella Assistant Professor, PhD  ·  702-895-2279  ·  kara.christensen@unlv.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Kansas, Wakarusa Research FacilityLawrence, Kansas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07060534