Richmond, VANCT05799872Now EnrollingIRB Ready

Anorexia Nervosa Clinical Trial in Richmond, VA

Access cutting-edge anorexia nervosa treatment through this clinical trial at a research site in Richmond. Study-provided care at no cost to qualified participants.

Sponsored by Virginia Commonwealth University

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Expert Care in Richmond

Access anorexia nervosa specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related anorexia nervosa treatment provided free

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Check if you qualify for this anorexia nervosa clinical trial in Richmond, VA

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Richmond

    Convenient for VA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Richmond site if eligible
  4. 4Begin participation

About This Anorexia Nervosa Study in Richmond

The investigators will recruit individuals with broadly-defined AN (n = 80) who are currently in or have recently participated in higher-level eating disorder treatment (e.g., residential, partial hospitalization/day treatment, intensive outpatient treatment). Interested participants will sign consent, complete eligibility assessments, and will be randomized to receive Positive Affect Treatment for Anorexia Nervosa (PAT-AN) or Psychoeducation and Behavioral Therapy (PBT) through teletherapy shortly following discharge from higher level of care. Participants can participate in most other forms of outpatient treatment while receiving the research intervention. Participants will engage in 24 weeks of PAT-AN or PBT starting in the first 3 months post-discharge. At each session, the investigators will complete brief measures assessing treatment acceptability, affect, and eating disorder symptoms. Participants will also complete an assessment battery of self-report, EMA, and neurocognitive measures evaluating primary outcomes (BMI; eating disorder symptoms), secondary outcomes (depression, anxiety, and suicidality), and presumed treatment mechanisms at baseline, end of treatment (EOT), and 3-month follow-up (FU). All assessments will be remotely delivered via HIPAA-compliant platforms.

Sponsor: Virginia Commonwealth University

Who Can Participate

Inclusion Criteria

Age \> or = 18 years old
Ability to read and speak in English
DSM-5 diagnosis of AN or atypical AN at admission to higher-level care
In higher-level care discharging to outpatient care or discharged to outpatient care within the past 3 months
Current BMI \> or = 18.5 kg/m2 (or will be by time of discharge)
BMI increase of \> or = 0.5 kg/m2 while in higher-level care
Ability to designate and sign a release of information for a primary physical or mental health provider for study duration
Willingness to participate in weekly assessments (e.g., weight monitoring) and audio or video recording of study therapy sessions for study duration
Access to a smartphone and/or computer permitting engagement in remote therapy and assessment.

Exclusion Criteria

Medical instability for outpatient care;
Lifetime DSM-5 primary psychotic or bipolar-I disorder
Current DSM-5 substance use disorder
Enrollment in outpatient therapy with highly overlapping content to PAT-AN

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Richmond?

Yes, this clinical trial (NCT05799872) has an active research site in Richmond, VA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Anorexia Nervosa Treatment Options in Richmond, VA

If you're searching for anorexia nervosa treatment options in Richmond, VA, this clinical trial (NCT05799872) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Richmond research site is actively enrolling participants for this clinical trial. You'll receive care from experienced anorexia nervosa specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all anorexia nervosa clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Richmond, VA