Efficacy Trial of a Dissonance Based Eating Disorder Program

Completed · Not applicable

Conditions studied: Eating Disorder

In brief

The purpose of this clinical trial is to investigate whether symptoms of disordered eating change among participants who complete an intervention. Participants will be randomly assigned to one of three intervention conditions and will undergo assessments of symptoms before, after, and 2 months after each intervention. Investigators are evaluating which interventions are most effective in reducing eating disorder symptoms and disorder-related psychological and cardiac risk factors.

Key facts

Study ID

NCT03796091

Run by

Cornell College

People needed

180

Starts

2018-11-18

Expected to finish

2021-04-15

Last updated by the study team

2022-12-09

Who can join

Age: 15 and older, up to 34. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Inclusion Criteria
• Women
• Age 15-34
• Postmenarcheal
• Premenopausal
• Subclinical or Clinical Eating Disorder Symptoms

You may not qualify if…

• Exclusion Criteria
• Must get physician clearance to participate if at medically high risk as defined in the protocol
• Must not be pregnant
• Must be able to read and speak English

Where it is running

• Cornell College Eating Disorder Institute — Mount Vernon, Iowa, United States

Full record on ClinicalTrials.gov

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