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Research Studies and Clinical Trials

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Clinical Trials and Other Research Studies

“Embrace the Data”  Daniel Le Grange, PhD, F.E.A.S.T. Advisor

Research and the Treatment of Eating Disorders

F.E.A.S.T. supports evidenced-based treatment of eating disorders. This means patient care must be based on verifiable data. This data primarily arises from research studies. Studies are designed to evaluate and compare the effects of different treatment approaches on health outcomes.

Since health care costs are often a serious burden, enrolling in a clinical trial may be seen as a way to obtain otherwise expensive care at no cost to participants. Generally speaking, participants in a clinical trial have a desire to find an effective treatment (benefit to self) and a desire to add to the body of knowledge for others suffering from the same disease (benefit to others).

All reputable clinical studies should undergo review by an institutional review board (IRB), also known as an independent ethics committee or ethical review board.

F.E.A.S.T. does not endorse any particular study. Our goal is to offer caregivers and patients who may be considering this option, information that can help with this determination. We believe the decision to participate in a clinical trial is highly individual and best made between caregivers and their medical and therapeutic team.

Email F.E.A.S.T. staff if you have a research study or survey you would like to have us post below.

Research Currently Seeking Participants:

Research Study For Females With Restrictive Eating Behaviors

~Posted at the request of the researcher Massachusetts General Hospital Neuroendrocrine Unit & Eating Disorders Clinical and Research Program “REACT is a 12-week study for…

Family Treatment Study for Adolescents with Anorexia Nervosa

FAMILY TREATMENT STUDY FOR ADOLESCENTS WITH ANOREXIA NERVOSA ~Posted at the request of the researcher Stanford University & The University of California, San Francisco Eating…

The TRIANGLE Project

~Posted at the request of the researcher Eating Disorders Unit at King’s College Anorexia Nervosa is a disorder that impacts on all domains of life.…

Survey For Those Caring For Someone With An Eating Disorder – UK

~Posted at the request of the researcher Promo video link: Survey link: Synopsis We would like to better understand the experiences of adults…

University of Canberra Research: Parents Seeking Help for Adolescence with Disordered Eating

~Posted at the request of the researcher My name is Eleanor I am a psychology honours student at the University of Canberra. I am currently…

Are You A Parent With An Experience Of Having An Eating Disorder?

~Posted at the request of the researcher University of Surrey We are looking for individuals with experiences of being parents with eating disorders to take…

Supporting eating disorder research related to Covid-19

F.E.A.S.T’s focus on evidence-based treatment comes from our support for scientific inquiry and data. Good treatment and results depend on the work of researchers asking…

Comparing Standard FBT and Guided Self-Help FBT


Diverse Families – FBT Model and Practice

-Posted at the request of the researcher Dear Family Based Treatment (FBT) Clinicians,  There is a growing need and desire for an understanding of how…

Online Program – Your Feedback Needed

– posted at the request of the author Hello, My name is Carolyn McCarter Wood. I am a licensed clinical social worker in Asheville NC.…

Important Considerations:

  • If you are considering a randomized interventional trial, it is important to review all of the treatment arms (control and interventions) that will be offered. Patients randomized into “control” groups would not receive the experimental treatment or medications that are under investigation. Typically, control groups would receive placebo medications or other traditional modes of treatment. If this would be a concern to your family, it is important to directly communicate that information to the investigation staff during the application process.
  • Patient safety requires that a complete and accurate medical history must be provided during the application process. It is essential to review the time commitment, special testing requirements, and all logistical aspects of study participation.
  • When considering a pharmaceutical interventional trial, carefully review the risks and benefits of medications being tested, including potential side effects.
  • After reviewing the study protocol, write down any questions you may have. You can ask for all answers to be provided in writing. Be sure you are comfortable with the protocols and objectives, care during and after study completion, the research team itself, and the setting where care will be provided. It’s important to consider how every requirement of participation will impact your family and your child, before consenting to any study.
  • You may speak with one of the investigators at any time if you have concerns about the study itself or other staff members.
  • We encourage all families considering this option for care to thoroughly review these questions.
  • Although you may withdraw at any time, it is best not to enroll in a study if you have reservations from the onset.
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