Actively Recruiting

Phase Not Applicable
Age: 5Years +
All Genders
Healthy Volunteers
ID07049861

Increasing Access to USPSTF-Recommended Obesity Care for Youth and Adults Who Are Recipients of Medicaid: Evaluation of a Comprehensive Multidisciplinary Obesity Care Training Program in FQHCs

Led by Washington University School of Medicine · Updated on 2026-05-20

6200

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

W

Washington University School of Medicine

Lead Sponsor

N

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating two training approaches for obesity care recommended by the US Preventive Services Task Force in Federally Qualified Health Centers. The study aims to compare patient weight changes, treatment use, primary care provider referrals, provider skills, and costs associated with these approaches. The research focuses on both youth and adults who receive Medicaid and have obesity, assessing the impact of different provider training methods. The trial compares a Comprehensive Multidisciplinary Obesity Care (CMOC) training program with an Implementation as Usual Control (IAUC) training. Provider trainees at participating centers will receive either CMOC or IAUC training during a 12-month period, followed by a 12-month sustainability phase. After the sustainability period, those initially in the IAUC group will be offered the CMOC training. CMOC training involves educating providers including medical staff, dietitians, and behavioral health providers to deliver guideline-based obesity care using screening, counseling, referrals, and intensive behavioral treatment supported by digital tools and community resources. Participants will be involved through provider trainees delivering care and benefit-eligible patients receiving obesity treatment at participating clinics. Outcomes will be measured by changes in patient percent overweight from 2 to 29 months after enrollment. Researchers will also monitor treatment use, provider referrals, care competencies, and costs. The study spans over two years of training and sustainability with ongoing assessments of both patient and provider outcomes throughout the trial period.

CONDITIONS

Brief Title

Advancing Biopsychosocial Care Training Initiative

Who Can Participate

Age: 5Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Provider trainees must be primary care providers, behavioral health providers, registered dietitians, or community health workers working at participating clinics.
  • Primary care providers must be medical doctors, doctors of osteopathic medicine, physician assistants, or nurse practitioners who can refer patients to intensive behavioral treatment and medical nutrition therapy and have completed residency if applicable.
  • Behavioral health providers must hold credentials such as licensed clinical social worker, licensed professional counselor, licensed marriage and family therapist, psychologist, psychiatric nurse practitioner, or psychiatrist.
  • Registered dietitians must be credentialed as registered dietitians or registered dietitian nutritionists.
  • Community health workers must work in a similar role within participating clinics.
  • Benefit-eligible patients must be youth aged 5 to 20 years or adults aged 21 and older, recipients of Medicaid, eligible for Missouri Medicaid benefit, have obesity, and have been seen at participating clinics.
Not Eligible

You will not qualify if you...

  • Provider trainees not working at participating clinics.
  • Primary care providers who cannot refer patients to intensive behavioral treatment or medical nutrition therapy.
  • Resident doctors.
  • Doctors specializing in reproductive health or related fields.
  • Patients without obesity.
  • Patients not on Medicaid.
  • Youth under 5 years of age.
  • Patients not seen at participating clinics.

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Training Period

Duration - 12 months

Participants undergo a 12-month training period to receive either the Comprehensive Multidisciplinary Obesity Care (CMOC) training or Implementation as Usual Control (IAUC) training.

Regular training sessions as scheduled over 12 months

Sustainability Period

Duration - 12 months

Participants continue to apply and sustain the training received during the prior 12 months over an additional 12-month period.

Periodic follow-up sessions during months 13 to 24

Trial Site Locations

Total: 1 location

1

Washington University School of Medicine

St Louis, Missouri, United States, 63110

Actively Recruiting

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Research Team

A

Aubrie Hampp, MSc

C

Corinne McMahon, MS, RDN, LD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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