Advancing Biopsychosocial Care Training Initiative

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age5+
SponsorWashington University School of Medicine

About this trial

This project will compare two training approaches for US Preventive Services Task Force recommended obesity care in Federally Qualified Health Centers (FQHC) across four aims. Aim 1 compares patient-level effectiveness \[i.e., patient relative weight change and the proportion of patients who achieve clinically significant weight loss\]. Aim 2 compares reach (patient treatment utilization). Aim 3 compares primary care provider (PCP) referrals to USPSTF-recommended care at 12 (adoption) and 24 months (maintenance) and short- and long-term changes in provider obesity care competencies . Aim 4 compares implementation and service costs.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Provider Trainees must be PCPs, BHPs, RDNs, or CHWs who work at participating clinics.

PCPs that are eligible to participate as Provider Trainees can be any of the following: Medical Doctors (MD), Doctor of Osteopathic Medicine (DO), Physician Assistants (PA), or Nurse Practitioners (NP). PCPs must see patients in a primary care setting and be capable of referring patients to IBT and MNT. PCPs must have already completed their residency (when applicable).

BHPs that are eligible to participate as Provider Trainees must be at least one of the following categories (listed with typical credentials): Licensed Clinical Social Worker (LCSW), Licensed Professional Counselor (LPC), Licensed Marriage and Family Therapist (LMFT), Psychologist (PhD/PsyD), Psychiatric Nurse Practitioner, Psychiatrist (MD).

RDNs that are eligible to participate as Provider Trainees must be Registered Dietitians/Registered Dietitian Nutritionists.

Disqualifiers

Not at a participating clinic

PCPs who do not have the ability to refer to IBT or MNT

Resident Doctors

A doctor specializing in reproductive health (or related fields)

Trial design

Design model

Parallel

Treatments tested in this trial

  • Comprehensive Multidisciplinary Obesity Care

    Other intervention

    CMOC is an innovative approach to obesity care delivery that leverages policy, clinical and community linkages, and digital technology for scalability. CMOC involves training providers (medical providers, registered dietitians, and behavioral health providers) to deliver guideline-based obesity care for youth and adults with obesity who receive Medicaid. Guidelines-based care involves screening, identification, weight counseling, and referral to intensive behavioral treatment by medical providers, and delivery of multicomponent intensive behavioral treatment by behavioral health providers and registered dietitians.

  • Implementation as Usual Control

    Other intervention

    The standard of care implemented in FQHCs in the absence of CMOC training.

Treatment groups

6,200 Participants
are divided into 2 treatment groups
Group A: CMOCActive comparator 1 intervention
Group B: IAUCActive comparator 2 interventions

Trial outcomes

Primary outcomes

1

Change in patient percent overweight

Percent over the median body mass index (BMI) for sex and age.

Time frame
Months 2-29 post-enrollment

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Washington University School of Medicine

Lead sponsor

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

Collaborator

Children's Mercy Hospital Kansas City

Collaborator

University of Missouri-Columbia

Collaborator

Missouri Institute of Mental Health

Collaborator

University of Missouri, Kansas City

Collaborator

The Missouri Department of Social Services, MO HealthNet Division, Office of Transformation

Collaborator