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Clinical Trials/NCT04980001
NCT04980001WithdrawnNot Applicable

Trauma Informed Childhood Obesity Care for Low-Income Minorities in Primary Care

Charles Drew University of Medicine and Science0 sitesStarted: June 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Withdrawn
Primary Endpoint
Health care provider satisfaction of FOCUS TIC-COM

Study Overview

Brief Summary

The purpose of this pilot study is to examine changes in childhood obesity associated with the implementation of a Trauma Informed Care approach with weight counseling and management among low-income minority children in a primary care setting.

Detailed Description

Prospective mixed methods pilot study, using both qualitative and quantitative measures. This study will be conducted in two phases. In Phase 1 (Year 1), the investigators plan to use a modified Delphi procedure called the RAND/UCLA Appropriateness Method in which the investigators will form a multidisciplinary panel to develop a consensus of incorporating the TIC practices based on FOCUS into current best practices for childhood obesity prevention and treatment among low-income minorities to be facilitated by primary care providers. In Phase 2 (Year 2), the investigators will train and implement the Primary Care Provider-mediated FOCUS TIC-COM among providers for obese children and their caregivers / parents in the MLK OPC Family Medicine Clinic. During this phase, the investigators plan to examine the feasibility and acceptability of delivering the FOCUS TIC-COM in the primary care setting at MLKOPC through surveys and focus groups with both providers and the parents / caregivers of overweight / obese children. The investigators will also explore whether the FOCUS TIC-COM impact on childhood obesity (as perceived by child's parent / caregiver) and increase linkages to behavioral health care regarding trauma / toxic stress. At 3 month intervals, the investigators will train a subset of providers in the intervention and they will implement the intervention immediately after training.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Adult Experts (>18 years old) in the fields of trauma informed care and childhood obesity among low-income minorities

Exclusion Criteria

  • Individuals outside of the fields of trauma informed care or childhood obesity
  • Inclusion Criteria:
  • Parents / Caregivers of overweight/obese children (ages 2-17 years old) in MLK-OPC who speak English or Spanish
  • Primary Care Providers (>18 years old) who work in the Family Medicine Clinic of the MLK-OPC
  • Exclusion Criteria:
  • Parents / Caregivers of children that are not overweight/obese and/or under 2 years old
  • Parent or caregiver that speaks a language other than English or Spanish
  • Primary Care Providers who do not work in the Family Medicine Clinic of the MLK-OPC

Outcomes

Primary Outcomes

Health care provider satisfaction of FOCUS TIC-COM

Time Frame: Last 6 months of Year 2 of study

The investigators plan to collect health care provider satisfaction in delivering the FOCUS TIC-COM. The investigators will measure satisfaction of various elements of the intervention using a 5 point Satisfaction Likert scale, where 1 means "very unsatisfied" and 5 means "very satisfied".

Parent / Caregiver satisfaction of FOCUS TIC-COM

Time Frame: Last 6 months of Year 2 of study

The investigators plan to collect parent / caregiver satisfaction in receiving the FOCUS TIC-COM intervention. The investigators will measure satisfaction of various elements of the intervention using a 5 point Satisfaction Likert scale, where 1 means "very unsatisfied" and 5 means "very satisfied".

Feasibility and acceptability of delivering FOCUS TIC-COM in the primary care setting, as perceived by caregivers/parents of low-income minority obese children and their providers

Time Frame: Last 6 months of Year 2 of study

The investigators will conduct focus groups with both health care providers and parents/caregivers of overweight/obese children exposed to FOCUS TIC-COM to assess intervention feasibility and acceptability. The investigators will ask questions in the focus group discussion on whether the Primary Care Provider-mediated FOCUS TIC-COM is relevant, appropriate and sustainable for the primary care setting and if the intervention should be disseminated. In addition, the investigators will examine the demand, practicality, adaptation, integration, expansion and efficacy of the intervention through the focus group discussion. The focus group questions will be derived from the RE-AIM framework: Reach into the target population; Effectiveness / Efficacy; Adaptation by target settings, institutions, and staff; Implementation - consistency and cost of delivery; Maintenance of intervention effects.

RAND/UCLA Appropriateness Method - Expert Panel Ratings / Consensus

Time Frame: Four rounds of rating over the course of 6 month to 1 year (Year 1 of study)

The investigators plan to use a modified Delphi procedure called the RAND/UCLA Appropriateness Method to reach consensus regarding the content and implementation of a Primary Care Provider-mediated FOCUS TIC-COM approach to address childhood obesity in low-income minority communities. The RAND/UCLA Appropriateness Method consists of four rounds of rating clinical indicators or practice guidelines derived from current literature on TIC that will be incorporated into the current standard of childhood obesity prevention and management. A benefit-to-cost ratio will be rated on a 9 point Likert scale, where 1 means that the expected harms greatly outweigh the expected benefits in relation to cost, and 9 means that the expected benefits greatly outweigh the expected harms in relation to cost. Necessity rating scale will be on a Likert scale of 1 to 9, where 1 means that the practice guideline is not necessary at all, and 9 means that the practice guideline is extremely necessary.

FOCUS TIC-COM Training Evaluation - Provider's Perceived confidence

Time Frame: Baseline and immediately after training (Year 2 of study)

The investigators plan to conduct a pre/post training evaluation measuring perceived confidence in FOCUS TIC-COM approach for overweight/obese children. The investigators will use a 5 point likert scale to measure confidence level in FOCUS TIC-COM approach, where 1 means "not confident at all" and 5 means "very confident". The 5 point likert scale for confidence has the following values: 1 means "not confident at all"; 2 means "not very confident"; 3 means "somewhat confident"; 4 means "fairly confident"; and 5 means "very confident".

Secondary Outcomes

  • Parent-reported linkages to behavioral health services(Last 6 months of Year 2 of study)
  • Calculated child BMI per parent / caregiver report(Last 6 months of Year 2 of study)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Angela Venegas

Assistant Professor

Charles Drew University of Medicine and Science

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