Eating Disorder Research, Studies, and Tests
To help further the treatment of eating disorders, Eating Disorder Hope maintains this list of studies which are seeking volunteers, and/or offer a free evaluation.
Scientific Exploration of Eating Disorders
The field of eating disorder research is continually evolving, and treatments are being developed and refined based on these discoveries. Given the complex nature of eating disorders, it is not surprising that the factors that contribute to these diseases are multifaceted. There is not one single cause responsible for the formation and development of an eating disorder, but rather, an accumulation of several possible compounding factors that each play a role in the development and maintenance of these diseases. These factors can be biological, sociological, emotional, environmental, etc.
One factor frequently investigated by researchers is the biological component of eating disorders. Many have pondered and theorized what mechanisms occur in the human body, and brain specifically, that can make an individual susceptible to developing anorexia, bulimia or binge eating disorder. Studies are currently underway that are examining potential contributing factors to an eating disorder, such as genetics, hormones, and neurobiology. Read this article to learn more about Scientific Developments and Research in Eating Disorders.
Eating Disorder Research & Studies
The WELL Center at Drexel University
The Balancing Act Study: Improving Weight Loss Outcomes for Binge Eating Behaviors
Project Description: Are you interested in losing weight? Do you also experience binge eating, emotional eating, or out of control eating? Researchers at the WELL Center at Drexel University are recruiting adults with binge eating behaviors for a research study designed to help individuals both lose weight and reduce binge eating episodes. Study participants must be age 18 or older and meet criteria for binge eating for participation in an outpatient group treatment study. Sign Up Today!
Compensation: Treatment is free and participants can receive up to $325.00.
The treatment will take place weekly at Drexel University. The treatment consists of 25 group sessions over one year, and there is a follow-up assessment one year after treatment ends.
The WELL Center at Drexel University
Project Description: This study aims to test a new smartphone application designed to enhance the gold-standard outpatient therapy treatment for bulimia nervosa. We aim to determine whether the efficacy of cognitive behavioral therapy for bulimia nervosa can be enhanced through a novel smartphone app designed to improve at-home use of therapeutic skills. Since the study involves testing a smartphone application, we are looking for participants who are comfortable using a smartphone and are willing to enter their food intake several times each day.
The study involves 16 sessions of outpatient individual therapy over the course of 16 weeks. Participants will meet with their therapist for approximately one hour, one time per week throughout treatment. All of the study assessments, as well as the individual therapy sessions, will occur on Drexel University’s campus, located in West Philadelphia. Study participants must be 18 or over and meet criteria for a primary diagnosis of bulimia nervosa to be eligible to participate. Sign Up Today!
Compensation: Participants will receive no-cost outpatient treatment and will be compensated for their participation in research assessments, up to $200.
If you are interested, please fill out an interest survey here (link to https://drexel.qualtrics.com/jfe/form/SV_1N57AEHbNOdWpN3), call 215.553.7130 or email [email protected]
The WELL Center at Drexel University
Project B.E.A.T. (Binge Eating Adolescent Treatment)
Project Description: Researchers at the WELL Center at Drexel University are recruiting adolescents with loss of control eating, binge eating, and/or purging for a study designed to help better understand the role of emotions in treatment. Adolescents must be between 12 and 18 years old and have parent permission to participate in an outpatient individual treatment study. They will receive 12 sessions of cognitive behavioral therapy (CBT) at the WELL Center over 3 months at no cost. Participants will undergo in-person assessments, during which they will complete surveys and wear non-invasive sensors that measure bodily responses like heart rate and skin sweating while completing computerized tasks. Sign Up Today!
Compensation: Participants will be enrolled in the study for about 6 months and can receive up to $140 in compensation.
If you are interested in participating, click the following link to schedule a time to speak with a research staff: https://calendly.com/wellcenter/phone-screen-child-adolescent.
The WELL Center at Drexel University
Project Recharge: Reward Change and Retraining Group Treatment for Eating Disorders
Project Description: This project is a group treatment study for individuals who experience loss of control eating. The treatment is designed to reduce the amount of reward that someone experiences from palatable foods by increasing the amount of reward experiences in other non-food areas of life. The group content is not directly focused on loss of control eating directly, but instead we expect that loss of control eating will improve indirectly as the imbalance between food and non-food based rewards is corrected. The group sessions will occur once a week for ten weeks and we expect that groups will begin in April 2019. As part of the study, all participants will complete two fMRI brain scans, before and after treatment, to examine changes in reward pathways in the brain.
Seeking individuals in the Philadelphia area between 18 and 70 years old who experience binge eating. Participants must be able to complete a one-hour fMRI scan. Sign Up Today!
Compensation: Participants will be compensated up to $325.
To see if you are eligible and schedule a phone call for more information, fill out our survey here: https://drexel.qualtrics.com/jfe/form/SV_dm7KMR3j8s1Finz or email: [email protected]
UCSD Eating Disorders Center for Treatment & Research
Project Description: Want to get a picture of your brain? Make some money? Maybe even travel to San Diego?! UC San Diego Center for Treatment and Research is excited to announce that there Research Registry is now open! Sign up today!
They are looking for children, teens, and adults to participate in our studies now, and in the future. They are currently recruiting people who currently have an eating disorder, who have recovered from an eating disorder, and people who have NEVER had an eating disorder. It takes 2 minutes to sign up and is free and confidential. When they have a study that is a match for you, they will contact you to see if you are interested.
Compensation: Study participants are compensated up to $375 and travel and lodging may also be reimbursed. If you are interested in participating in a study now or in the future please fill out this SURVEY.
UCSD Eating Disorders Center for Treatment & Research
Project Description: The University of California San Diego Eating Disorders Center for Treatment and Research is recruiting women recovered from anorexia nervosa (with no history of bulimia nervosa) between the ages of 18-45 to participate in a research study. We require that our participants be drug and medicine free for at least 3 months (birth control is okay), as well as be behavior/ symptom-free for at least 12 months. This research study uses fMRI to assess how the brains of individuals who have recovered from eating disorders may respond differently during tasks related to various sensations. Functional Magnetic Resonance Imaging (fMRI) techniques use powerful magnetic fields that allow a scanner and a computer to take very detailed pictures of the structure of the brain and brain activation.
This study would involve a 4.5-hour commitment, with two and a half hours in the MRI scanner. During the scan you would do two different tasks: one task would measure attention while hearing a loud noise in the scanner and the other task is an associative learning task that involves determining where to categorize two different photos.
Compensation: Participants will be compensated $200 dollars for the single visit. Depending on the participants’ current location, we cover travel expenses as well as one-night hotel stay for the visit.
For more information: Please call (858)246-2660 or email [email protected] You may also visit our website at: http://eatingdisorders.ucsd.edu/research/our-research.html
Project Name: Self-Regulatory Control in Bulimia Nervosa
Description: This research use fMRI to assess how the brains of individuals who currently have eating disorders may respond differently when inhibiting responses and regulating emotions. Participants will complete diagnostic interviews and assessments. In the scanner, participants will complete two task. The first involves pressing buttons in response to certain pictures, and the second involves viewing different neutral or emotional images and using emotional regulation strategies taught during screening.
Who may be eligible: Right-handed females between the ages of 18-35 who currently have bulimia nervosa.
Compensation: Participants are compensated up to $225. Depending on the participant’s current location, we can cover travel expense (up to 150 miles) as well as a one night hotel stay for the visit.
For more information: Contact Joanna Chen at (858)-543-0371 or email [email protected]
We are currently recruiting for three studies utilizing a technology called magnetic resonance imaging (MRI).
MRI techniques use powerful magnetic fields that temporarily magnetize some of the chemicals in your brain, which allows a scanner and a computer to take a very detailed picture of the structure of your brain.
- Project Name: Neurobiology of Anorexia and Bulimia. Description: This study is designed to assess brain response to different types of sensation. You would be compensated $200 for this single visit. We are recruiting women between the ages of 18 -45. We require that our participants be drug and medicine free for at least 3 months (birth control is okay), as well as be behavior/ symptom-free for at least 12 months if you have recovered from an eating disorder.
- Project Name: Neurobiology of Reward and Decision-Making in Bulimia Nervosa. Description: This MRI study is also a one-hour scan session for which participants will be compensated up to $200 for taking part. We are recruiting women between 15 and 30 years old. Participants must be drug and medicine free for at least 3 months (birth control is okay). Participants may currently have or be recovered (behavior/ symptom-free for at least 12 months) from bulimia nervosa or may have never had an eating disorder.
- Project Name: Neural Bases of Multiple Forms of Self-Regulatory Control in Bulimia Nervosa. Description: This third MRI study requires three hours of interview and assessment time with a one-hour scan session for which participants will be compensated up to $200 for taking part. We are recruiting women between 15 and 35 years old. Participants must be drug and medicine free for at least 3 months (birth control is okay). Participants may currently have bulimia nervosa and engage in purging behaviors or may have never had an eating disorder.
For more information: Please email [email protected]
Massachusetts General Hospital Research Study
Project Name: Effects of Anorexia Nervosa on Peak Bone Mass
Project Description: Massachusetts General Hospital is conducting a research study to learn how to improve bone density in young women 14-22 years of age who are low weight or suffering from anorexia nervosa. This is a 12-month long study with up to 10 outpatient visits at MGH and compensation of up to $910. The study includes bone density, hormonal, and nutritional evaluations at no cost.
For more information: Please contact Meghan Slattery, NP at [email protected] or (617) 643-0267
Survey: Click on this link to take our Eligibility Survey: Massachusetts General Hospital Bone Density Study
*Click on Image to View PDF
Stanford University Research Study
Project Name: Qsymia (phentermine-topiramate) to Reduce Binge-Eating/Purging in Patients with Binge Eating Disorder and Bulimia Nervosa
Project Description: This study aims to test the efficacy of an FDA approved drug for obesity, Qsymia, for reducing symptoms of binge eating and/or purging in participants with binge eating disorder and bulimia nervosa, compared to a control medication. All study participants will receive the study medication– either in the first half of the study or in the second half of the study. Neither you nor members of the research team will know the order in which you receive them until the end of the trial. Medication is provided at no cost and the study is expected to take up to 6 months.
Ages: Men and women aged 18-60 with current symptoms of binge eating and/or purging
For More Information: Please contact Hannah at [email protected] or at (650)-723-2242.
Click on the PDF for more information.
The Chicago School of Professional Psychology seeks female volunteers for study
Project Name: Adolescent’s Experience of Anorexia with a Friend; A Phenomenological Study
Project Description: Various research has suggested that adolescent female friends share similar attitudes and behaviors toward body image concerns and dieting. While the importance and influence of friends have been examined, one area that lacks research and understanding is the role that a friend who has previously suffered from anorexia plays in a friend’s current experience with anorexia. The proposed research aims to eliminate this gap in understanding through a phenomenological study involving in-depth interviews with six females who suffered from anorexia nervosa during adolescence.
Seeking females 18+ who have recovered from anorexia nervosa within the past five years. Specifically seeking those who had a friend who also struggled with anorexia nervosa during or prior to the friendship.
For more information, contact Hillary Urban at [email protected] or call 810-623-7659.
Researchers from Deakin University, School of Psychology Seek Volunteers for Eating Disorder Study
Project Name: Profiling the early maladaptive schemas, schema modes, and eating disorder behaviors in eating disorder subgroups.
Project Description: Eating disorders (EDs) are associated with severe psychological and physiological impacts. ED affected individuals often hold chronic and rigid beliefs and tend not to respond to standard psychological treatments, suggesting a more focused, sophisticated and intensive treatment approach such as Schema Therapy and Schema Mode therapy might be needed.
The aim of this study is to profile the patterns of specific Early Maladaptive Schemas (EMSs) and Schema Modes (SMs) in ED groups. EMSs are one’s unhelpful beliefs about themselves, others, and the world around them. These beliefs are developed in childhood and adolescence and built upon throughout one’s life. SMs are a combination of these schemas and coping behaviors that are either adaptive or maladaptive and present at any particular moment. Gaining insight into the underlying belief system can be critical in the ongoing optimization of clinical assessment and treatment of EDs.
Type of Research:
This is a Ph.D. research at Deakin University, Australia
It uses the online survey method.
The online anonymous survey can be accessed at:
Target Audience: We are looking for adult females and males who self-identified as suffering from an eating disorder.
This study has been approved by Deakin research ethics committee on 13/01/2015.
Researcher from The City University London, School of Social Sciences, Seeking Volunteers
Project Name: Feelings and Faces
Purpose of Study: Researchers are looking at the reasons why some people have difficulties with impulsive behaviours, such as self-harm and what their feelings are around food. This study aims to look at how people pick up on what others are thinking and feeling, as well as how people think about their own thoughts and feelings. Greater knowledge in this area will help in designing better psychological therapies for people who have impulsive behaviours or strong feelings they find it difficult to deal with.
If you suffer from an eating disorder with/without self-harm and are interested in participating in a research study about feelings & faces, please access the survey here.
This research has been approved by City University and the NHS. If you would like to ask more questions about the research, please contact Angie Cucchi on 07930 645428 or email: [email protected]
Various Research Studies for Women with Anorexia Nervosa
The Neuroendocrine Unit at Massachusetts General Hospital is offering a variety of research studies for women with anorexia nervosa. We are currently researching different methods of treatment for bone loss, anxiety & depression, and gastrointestinal issues in women with anorexia nervosa. If you are interested in participating, take this brief pre-screening survey – https://redcap.partners.org/redcap/surveys/?s=7D5MTI
Massachusetts General Hospital Neuroendocrine Unit
Doctoral Student at Fordham University Performing Study – Participants Requested
Doctoral Student would like to invite you to consider participating in an anonymous study that examines factors that may be related to Anorexia Nervosa severity. The results of this study will help treatment providers better identify early warning signs of Anorexia Nervosa and create more tailored treatment plans.
To be eligible for this study, you must be (1) between the ages of 12 and 18; (2) have previously had or currently be receiving professional treatment for Anorexia Nervosa; and (3) have parental permission to participate.
Participation will involve completing a series of online questionnaires, which will take approximately 30 minutes. You will not be asked to provide your name at any time. Publications or presentations about the research will not include individual responses, only summary data on all participants.
If you would like to participate in this online study, please visit: www.surveymonkey.com/s/M65K9GC
*Participants have a chance to win a $50 Amazon gift card by participating in this study!
Study on Anorexia Nervosa and Religious Coping Styles
Graduate student at Richmont Graduate University is conducting a study aimed at distinguishing how religious coping methods and views of God’s grace affect and interact with Anorexia Nervosa.
WHO CAN PARTICIPATE?
Males and females age 18 or older who:
- claim Christianity as their religion;
- have been diagnosed with Anorexia Nervosa;
- care read at the 6th-grade level; AND
- are willing to spend 20 to 35 minutes answering questions on online questionnaires.
To participate in the study, please visit the following website:
WHAT WILL HAPPEN?
Complete five online questionnaires at your own pace, on your own time, and in the comfort of your own home!
No identifying information will be requested.
This study has received approval from the Richmont Graduate University Human Subjects Committee. Primary investigators for this study are DeAnne Terrell, Ph.D., Dean of Students, Richmont Graduate University, and Katie Rider, BA, Master of Arts in Professional Counseling student, Richmont Graduate University.
For more information, please visit the following website www.mannafund.org or contact Katie Rider at 678-235-5917 or [email protected].
Dyadic Adjustment in Mothers of Children with Anorexia
Are you the mother of a child who is currently receiving outpatient treatment for Anorexia Nervosa? If so, we’d like to invite you to participate in an anonymous study that examines the experience of caring for a child with Anorexia Nervosa. This study will look at how a child’s eating disorder affects the parents and family, and how families cope with caring for a child with Anorexia. We hope these research findings will provide greater insight into how a child’s illness affects families so that more support services can be developed to help parents and caregivers. To be eligible for this study, you must be the mother of a child with Anorexia and currently be in a committed relationship. If your child is between the ages of 10-21, is currently receiving outpatient treatment for Anorexia Nervosa, and is currently living with you and your spouse/partner at home, we invite you to participate in this important study. Participation will involve: Completing the questionnaire online will take approximately 15-30 minutes. You will not be asked to provide your name at any time– Publications or presentations about the research findings will not include individual responses, only summary data on all participants will be presented. If you would like more information about this study, please contact Marissa Alexander at [email protected], or Dr. Merle Keitel at [email protected]
To participate in this study, click on the following link: https://www.surveymonkey.com/s/6QPPY8M
Newly proposed DSM-5 criteria reduce the need for not otherwise specified diagnoses and can be reliability applied by clinicians in a residential eating disorder treatment setting
Jennifer J. Thomas, Ph.D.1,2,3; Kamryn T. Eddy, Ph.D.2,3;
Robert Hohe, B.S.1,2,4; Philip Levendusky, Ph.D. 1,3; Anne E. Becker, M.D., Ph.D., Sc.M.2,3,5
1Klarman Eating Disorders Center, McLean Hospital, Belmont, MA, USA
2Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA
3Department of Psychiatry, Harvard Medical School, Boston, MA, USA
4Technical University of Dresden, Dresden, Germany
5Department of Global Health & Social Medicine, Harvard Medical School, Boston, MA, USA
Objective: The DSM-5 Eating Disorders (ED) Work Group has proposed new diagnostic criteria that broaden anorexia nervosa (AN) and bulimia nervosa (BN); add new disorders (e.g., binge eating disorder, avoidant/restrictive food intake disorder); and create descriptive subtypes within ED not otherwise specified (EDNOS). However, the reliability and validity of these new criteria have not been prospectively tested. The purpose of this study was to evaluate the clinical utility of proposed DSM-5 criteria by assessing the prevalence of EDNOS under DSM-IV versus DSM-5; and the inter-rater reliability of research and clinician diagnoses in DSM-IV versus DSM-5.
Method: Consecutive female patients aged 13-23 (N = 42) admitted to a residential ED treatment facility received both DSM-IV and DSM-5 ED diagnoses from a research assessor (n = 3) via the Eating Disorder Examination, and a treating clinician (n = 13) via an unstructured interview in routine care. We tested our hypothesis that significantly fewer patients would receive EDNOS diagnoses under DSM-5 versus DSM-IV using Fisher’s exact test, and evaluated inter-rater reliability between research and clinician diagnoses using Cohen’s kappa.
Results: As hypothesized, significantly fewer patients received EDNOS diagnoses from researchers under DSM-5 (n = 14; 33%) versus DSM-IV (n = 30; 71%), p = .003. Clinicians also conferred fewer EDNOS diagnoses under DSM-5 (n = 7; 17%) than DSM-IV (n = 14; 33%), p = .003. While research and clinical diagnoses showed moderate inter-rater reliability under DSM-IV (Îº = .41), they showed substantial reliability under DSM-5 (Îº = .62).
Conclusion: Our preliminary data suggest that the proposed DSM-5 revisions will successfully reduce the predominance of EDNOS in this naturalistic clinical setting. Importantly, the observed improvement in clinical utility is not associated with a reduction in inter-rater reliability, suggesting that clinicians can reliably apply the new criteria in routine care.
Johns Hopkins Eating Disorder Program Researching Effectiveness of a Research Medication in the Treatment of Anorexia Nervosa
The Johns Hopkins Eating Disorders Program is seeking adults aged 18-55 to participate in a placebo-controlled trial to examine the effectiveness of a research medication in the treatment of anorexia nervosa. Participants will be offered 16 weeks of medication (active or inactive) and weekly outpatient medical monitoring by a psychiatrist. The treatment will be provided at no cost and participants will receive up to $250 for completing all parts of the study. To participate, you must have anorexia nervosa, be 18-55 years old, be medically stable for outpatient treatment, and willing to complete assessments (interviews, questionnaires and medical evaluations) at intervals throughout the 16-week study and at 1- and 2-month follow-ups. All information gathered will remain confidential. Please call (410) 955-3863 for more information or email Angela Guarda at [email protected], or visit information.