Philadelphia, PANCT06817863Now EnrollingIRB Ready

Binge Eating Disorder Associated With Obesity Clinical Trial in Philadelphia, PA

Access cutting-edge binge eating disorder associated with obesity treatment through this phase 1/2 clinical trial at a research site in Philadelphia. Study-provided care at no cost to qualified participants.

Sponsored by Drexel University

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Expert Care in Philadelphia

Access binge eating disorder associated with obesity specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related binge eating disorder associated with obesity treatment provided free

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Check if you qualify for this binge eating disorder associated with obesity clinical trial in Philadelphia, PA

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Why Participate?

  • No-Cost Study Care

  • Local to Philadelphia

    Convenient for PA 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 Philadelphia site if eligible
  4. 4Begin participation

About This Binge Eating Disorder Associated With Obesity Study in Philadelphia

The proposed study is an open label, non randomized, waitlist controlled single group feasibility study of the feasibility and usability of a digital intervention (called ChangeBite) to be used by individuals with obesity and comorbid binge eating behavior. The proposed research will include approximately 30 participants. Participants will be recruited for this single group pilot trial using online advertising to attend a virtual screening session. Screened participants willing and eligible to participate, will receive informed consent and formally start ChangeBite. Participants will be instructed to engage with ChangeBite and attend follow up assessments on scheduled video calls. Feasibility and acceptability of implementation will be assessed by collecting data on recruitment, retention, usability and satisfaction. The research team will also collect assessment data from participants on feasibility, and usability. In addition to self report scales, semi-structured interviews will be completed with a trained research team member via video call and will be partially recorded. Assessments will be done at baseline, 12 weeks, and 24 weeks. Participants' app use frequency and duration will be tracked using software analytics. Participants' body weight will be captured weekly using a timestamped picture of their weight as it appears on their scale and Body Mass Index will be calculated with these data points.

Sponsor: Drexel University

Who Can Participate

Inclusion Criteria

Are English speaking male or female
Are aged 18-70 years
Have recurrent objective or subjective binge eating episodes (≥12 episodes in 3 months)
Have BMI ≥30
Own an iPhone with iOS 11 or higher, or Android with OS 8.1 or higher
Are willing and able to complete enrollment procedures
Are able to understand the nature of the study and provide written informed consent

Exclusion Criteria

Are unable to fluently speak, write and read English.
Are already receiving treatment for an eating disorder (e.g., research participants cannot be receiving concurrent eating disorder treatment from another provider)
Are receiving weight loss treatment (behavioral or pharmacological)
Have a mental handicap or are currently experiencing severe psychopathology that would limit their ability to engage in study (e.g., imminent or high risk for suicide, substance use disorder, active psychotic disorder,)
Are purging and/or using laxatives 3 or more times per week and are not deemed safe for remote treatment by a primary care provider.
Are exercising 2 or more hours a day on average, or engaging in significantly harmful compensatory behaviors (i.e., \> 3x/week of self-induced vomiting or laxative use), and are not deemed safe for remote treatment by a primary care provider.
Are fasting for 24 hours or more, \> 3x times a week, and are not deemed safe for remote treatment by a primary care provider.
Are unwilling to receive medical clearance and/or medical monitoring as requested by the study to ensure they are medically safe to participate.
Are pregnant or planning to become pregnant within the next year.
Are individuals who are not yet adults (infants, children, teenagers) Are currently taking any of these medications: Haldol, Loxitane, Mellaril, Moban, Navane, Prolixin, Serentil, Stelaxine, Trilafon, Thoraxine, Abilify, Clozaril, Geodon, Risperdal, Seroquel, Zyprexa
Are adults unable to consent
Are prisoners

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 Philadelphia?

Yes, this clinical trial (NCT06817863) has an active research site in Philadelphia, PA 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.

Binge Eating Disorder Associated With Obesity Treatment Options in Philadelphia, PA

If you're searching for binge eating disorder associated with obesity treatment options in Philadelphia, PA, this clinical trial (NCT06817863) 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 Philadelphia research site is actively enrolling participants for this phase 1/2 clinical trial. You'll receive care from experienced binge eating disorder associated with obesity 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 binge eating disorder associated with obesity clinical trials near you to find additional studies recruiting in your area.

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