The proposed study tests fear, gut peptide response, and perceptions of fullness as causes of gastrointestinal distress and eating disorder maintenance.
Age range
18 Years – 40 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Subjective Rating of Fear
Timeframe: -10 minutes, 0 minutes (immediately after the intervention), and 10 minutes post-intervention
Difference in Average Skin Conductance
Timeframe: -10 minutes, 0 minutes (immediately after the intervention), and 10 minutes post-intervention
Gastrointestinal Distress
Timeframe: -10 minutes, 0 minutes (immediately after the intervention), and 10 minutes post-intervention
Cholecystokinin Response
Timeframe: 0 minutes (immediately after the intervention), 10 minutes, 20 minutes, 30 minutes, 60 minutes and 90 minutes post-intervention
Peptide YY Response
Timeframe: 0 minutes (immediately after the intervention), 10 minutes, 20 minutes, 30 minutes, 60 minutes and 90 minutes post-intervention
Subjective Rating of Fullness
Timeframe: 0 minutes (immediately after the intervention), 10 minutes, 20 minutes, 30 minutes, 60 minutes and 90 minutes post-intervention
Urges to Restrict Food Intake
Timeframe: 60 minutes post-intervention