Anorexia Research Study
Researchers at Johns Hopkins University are conducting a study on the gastrointestinal peptide response to food and how it may affect food choice.
Fast Facts
Women Ages 13-70
Diagnosis or Strong Suspicion of Anorexia
Compensation Provided
Conducted in Baltimore, MD
Study Background
Johns Hopkins University is looking for women with anorexia to participate in a gut peptide study.
This research is being done to understand the effect of behavioral treatment and meal-based restoration on the gastrointestinal peptide response in anorexia nervosa (AN).
We will ask participants to complete three in-person visits consisting of a screening, blood draws, and computer tasks, and an MRI scan.
Findings from this research study could provide new information about the relationship of the gastrointestinal (GI) tract in anorexia nervosa and how this may influence treatment response.
Further research and join our compensated study!
Study Background
Johns Hopkins University is looking for women with anorexia to participate in a gut peptide study.
This research is being done to understand the effect of behavioral treatment and meal-based restoration on the gastrointestinal peptide response in anorexia nervosa (AN).
We will ask participants to complete three in-person visits consisting of a screening, blood draws, and computer tasks, and an MRI scan.
Findings from this research study could provide new information about the relationship of the gastrointestinal (GI) tract in anorexia nervosa and how this may influence treatment response.
Further research and join our compensated study!
Additional Information
The purpose of this research study is to learn more about the gastrointestinal peptide response to food and how it may affect food choice in women with anorexia.
You may qualify for this study if you meet the following criteria.
Inclusion Criteria:
- Women ages 13-70
- Diagnosis of anorexia or strong suspicion of anorexia
- Able to speak and understand English
- BMI < 18.5
- Able to undergo MRI (no metal in the body, no claustrophobia)
Once enrolled, this study involves:
- Visit 1: Providing informed consent and consuming a 15 fl oz. Ensure meal (0.5 hrs)
- Visit 2: Consuming an Ensure meal and completing computer-based questionnaires while undergoing blood draws (3.5 hrs)
- Visit 3: Consuming an Ensure meal and completing an MRI scan (0.5 hrs)
Compensation is provided up to $200 for your participation.
There is no cost for you to participate in our research study.
