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Dissemination and Implementation of Improving Pediatric Obesity Practice Using Prompts (iPOP-UP)

Primary Purpose

Obesity, Childhood

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Improving Pediatric Obesity Practice Using Prompts (iPOP-UP)
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Obesity, Childhood focused on measuring Clinical Decision Support, Implementation Science, Pediatric Obesity

Eligibility Criteria

2 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Primary Care Practices: all primary care practices using the EHR system of one of the 3 health systems participating in the study that agree to participate in the iPOP-UP trial; Clinician-participants: all clinicians who delivery pediatric primary care at the participating practices, including physicians and physicians-in-training (residents and fellows), physician assistants (PA), nurse practitioners (NP)/advanced practice registered nurses (APRNs); Patient-participants: all patients ages 2-18 with overweight/obesity seen during the study period may be impacted by the intervention. A limited dataset will be collected for the subset of these 2 to 18 years old patients with BMI ≥ 85th percentile for age and sex seen for a well or follow-up visit during the study period in a primary care department and conducted by a prescribing clinician (physician, NP, PA) Exclusion Criteria: None - exclusion criteria are purposefully limited in this real-world implementation study

Sites / Locations

  • Eskenazi HealthRecruiting
  • Duke UniversityRecruiting
  • Children's Hospital of PhiladelphiaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Clinical Decision Support Tool

Control

Arm Description

Practices assigned to iPOP-UP intervention which involves EHR-based CDS tools refined through a formative evaluation and user-centered design.

Practices assigned to usual care that will not have access to the iPOP-UP CDS tool but will have access to many opportunities available to all pediatric clinicians nationally around the release of the new American Academy of Pediatrics guidelines for obesity management.

Outcomes

Primary Outcome Measures

Change in %BMIp95
Change in %BMIp95, calculated from height and weight measured as part of routine clinical practice during primary care clinic visits and documented in the electronic health record. A negative percentage indicates that the participant's BMI has decreased since trial launch.
Change in composite measure of clinician's adherence to clinical guidelines, for visits completed among children 2-18 years-old with BMI ≥85th percentile.
Six-month change in composite measure of adherence to clinical guidelines, calculated from practice behaviors queried from the electronic health record. A dichotomous variable, adherence is defined as whether or not, for each relevant visit, the clinician followed all evidence of recommended obesity-related care during the study period: Inclusion of diagnosis code indicating high BMI in visit diagnosis associated with the visit or as an active diagnosis in the problem list Recommended lab orders for obesity related comorbidities, if eligible Appropriate BP measurement in children 3 and older Counseling diagnosis codes or structured documentation (every visit) Follow-up visit requested at visit or active referral order for further management of obesity A score of 1 indicates that a clinician followed all evidence of recommended obesity-related care; a score of 0 indicates that a clinician did not follow at least one recommendation for obesity-related care.

Secondary Outcome Measures

Change in composite measure of clinician's adherence to clinical guidelines
Change from baseline through 12 and 18 months in composite measure of adherence to clinical guidelines, calculated from practice behaviors queried from the electronic health record. A dichotomous variable, adherence is defined as whether or not, for each relevant visit, the clinician followed all evidence of recommended obesity-related care during the study period: Inclusion of diagnosis code indicating high BMI in visit diagnosis associated with the visit or as an active diagnosis in the problem list Recommended lab orders for obesity related comorbidities, if eligible Appropriate BP measurement in children 3 and older Counseling diagnosis codes or structured documentation (every visit) Follow-up visit requested at visit or active referral order for further management of obesity A score of 1 indicates that a clinician followed all evidence of recommended obesity-related care; a score of 0 indicates that a clinician did not follow at least one recommendation
Change in inclusion of diagnosis code indicating high BMI in problem list
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of inclusion of diagnosis code indicating high BMI in problem list, queried from the electronic health record at baseline, 6, 12, and 18 months to see change at 6 months and how it's sustained at 12 and 18 months. A higher proportion of visits with relevant diagnosis code is consistent with recommended care.
Change in inclusion of diagnosis code indicating high BMI in visit diagnosis
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of inclusion of diagnosis code indicating high BMI queried from the electronic health record. A higher proportion of visits with relevant diagnosis code is consistent with recommended care.
Change in adherence to guideline recommended screening lab orders for obesity related comorbidities, if eligible
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of screening lab orders for obesity-related comorbidities recommended by the American Academy of Pediatrics clinical practice guideline for obesity based on age and BMI percentile, queried from the electronic health record. A higher proportion of visits with recommended screening lab orders is consistent with recommended care.
Change in appropriate blood pressure screening in children 3 and older
Visits completed among children 3-18 years with BMI ≥85th percentile during the study period with evidence of appropriate blood pressure screening queried from the electronic health record. A higher proportion of visits with blood pressure screening is consistent with recommended care.
Change in structured documentation of counseling
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of counseling structured documentation queried from the electronic health record. A higher proportion of visits with counseling structured documentation is consistent with recommended care.
Change in follow-up visit requested
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of follow-up visit requested, queried from the electronic health record. A higher proportion of visits with follow-up visit requested is consistent with recommended care.
Change in referral for further management of obesity
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of referral for further management of obesity queried from the electronic health record. A higher proportion of visits with follow-up or referral for further management of obesity is consistent with recommended care.
Change in weight loss medication orders, if eligible
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of weight loss medication orders, if eligible, queried from the electronic health record. A higher proportion of visits with weight loss medication orders, when eligible, is consistent with recommended care.
Change in bariatric surgery program referrals, if eligible
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of bariatric surgery program referrals, if eligible queried from the electronic health record. A higher proportion of referrals to bariatric surgery programs, when eligible, is consistent with recommended care.
Change in potentially unnecessary insulin or thyroid laboratory tests ordered
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of insulin or thyroid lab orders, not routinely recommended for evaluation of children with obesity, queried from the electronic health record. A lower proportion indicates better adherence to recommended care.
Clinicians' utilization of the clinical decision support tools
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of clinician use of the clinical decision support tools in the electronic health record developed for this trial, calculated from electronic health record query. Measure= % of visits at intervention sites at which the clinicians' uses clinical decision support tools through18 months A higher proportion indicates greater utilization of clinical decision support tools.
Change in clinicians' attitudes and practice around managing elevated BMI in primary care
Change in clinician's attitudes and practice around management of elevated BMI measured using survey questions; Possible responses range from 1 (strongly disagree) to 5 (strongly agree) for attitudes or 1 (never) to 5 (almost always).
Cost and cost-effectiveness of iPOP-UP
Site-specific costs of implementing iPOP-UP per practice site and per patient incremental cost of iPOP-UP compared with usual care. Calculated based on study team logs, EHR data on healthcare utilization, and surveys of clinicians.

Full Information

First Posted
November 15, 2022
Last Updated
May 11, 2023
Sponsor
Yale University
Collaborators
National Institute on Minority Health and Health Disparities (NIMHD)
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1. Study Identification

Unique Protocol Identification Number
NCT05627011
Brief Title
Dissemination and Implementation of Improving Pediatric Obesity Practice Using Prompts
Acronym
iPOP-UP
Official Title
Dissemination and Implementation of Decision Support for the Management of Overweight and Obesity in Pediatric Primary Care - Improving Pediatric Obesity Practice Using Prompts
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 9, 2023 (Actual)
Primary Completion Date
November 30, 2024 (Anticipated)
Study Completion Date
November 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yale University
Collaborators
National Institute on Minority Health and Health Disparities (NIMHD)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the dissemination and implementation of electronic health record-based clinical decision support tools for the management of pediatric overweight and obesity in primary care.
Detailed Description
This study will evaluate iPOP-UP, a newly-optimized intervention to improve adherence to national guidelines for the management of childhood obesity, among 84 primary care practices affiliated with three health systems serving children with racial and ethnic, socio-economic, rural-urban, and geographic diversity. This multi-site, parallel 2-arm cluster randomized controlled "Hybrid Type 2" effectiveness-implementation trial will use mixed methods (electronic health record (EHR) data analysis, surveys, interviews, and focus groups) to simultaneously evaluate (1) the effectiveness of the iPOP-UP implementation package in improving clinical care and children's BMI outcomes in pediatric primary care setting and (2) the impact of the implementation strategy on the reach, adoption, fidelity, cost, and maintenance of the intervention. The unit of randomization in this study is pediatric primary care practices. Within the participating 84 practices, pediatric primary care clinicians working at the implementation sites will be invited to participate in pre- and post-intervention surveys assessing their practice behaviors, obesity-related attitudes, beliefs, and self-efficacy, EHR usage and attitudes, and training preferences. In addition, a limited data set of EHR from patients visits will be queried and analyzed to evaluate clinical care outcomes and children's BMI outcomes. Limited data (to include dates and geographic information but no facial identifiers) will be queried and analyzed for all children 1) age 2.0 to ≤18 years-old at baseline, 2) with a well-child visit, during which height and weight are measured, at one of the participating practices during the study period, and 3) with a BMI ≥85th percentile for age/sex (CDC criteria for overweight/obesity). Outcomes include: (a) change in BMI, measured as the yearly change in BMI expressed as a percentage of the 95th percentile (%BMIp95); (b) Change in clinicians' objective practice around managing elevated BMI in primary care using EHR data; (c) Change in clinicians' self-reported knowledge, attitudes, and practice around managing elevated BMI in primary care; and (d) Utilization of Clinical Decision Support (CDS) tools. The investigators will also describe implementation outcomes (reach, adoption, fidelity/adaptation, and cost) through qualitative and quantitative data collection from members of the study team throughout the process of implementation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Childhood
Keywords
Clinical Decision Support, Implementation Science, Pediatric Obesity

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This is a multi-site, parallel 2-arm cluster randomized controlled trial "Hybrid Type 2" effectiveness-implementation study to simultaneously evaluate (1) the effectiveness of iPOP-UP in improving clinical care and child weight outcomes in pediatric primary care setting and (2) the impact of the implementation strategy on the reach, adoption, fidelity, cost, and maintenance of the intervention.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
240772 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Clinical Decision Support Tool
Arm Type
Experimental
Arm Description
Practices assigned to iPOP-UP intervention which involves EHR-based CDS tools refined through a formative evaluation and user-centered design.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Practices assigned to usual care that will not have access to the iPOP-UP CDS tool but will have access to many opportunities available to all pediatric clinicians nationally around the release of the new American Academy of Pediatrics guidelines for obesity management.
Intervention Type
Behavioral
Intervention Name(s)
Improving Pediatric Obesity Practice Using Prompts (iPOP-UP)
Intervention Description
EHR-based CDS tools refined through a formative evaluation and user-centered design process that immediately preceded this study.
Primary Outcome Measure Information:
Title
Change in %BMIp95
Description
Change in %BMIp95, calculated from height and weight measured as part of routine clinical practice during primary care clinic visits and documented in the electronic health record. A negative percentage indicates that the participant's BMI has decreased since trial launch.
Time Frame
Up to 15 months after first primary care visit following trial launch
Title
Change in composite measure of clinician's adherence to clinical guidelines, for visits completed among children 2-18 years-old with BMI ≥85th percentile.
Description
Six-month change in composite measure of adherence to clinical guidelines, calculated from practice behaviors queried from the electronic health record. A dichotomous variable, adherence is defined as whether or not, for each relevant visit, the clinician followed all evidence of recommended obesity-related care during the study period: Inclusion of diagnosis code indicating high BMI in visit diagnosis associated with the visit or as an active diagnosis in the problem list Recommended lab orders for obesity related comorbidities, if eligible Appropriate BP measurement in children 3 and older Counseling diagnosis codes or structured documentation (every visit) Follow-up visit requested at visit or active referral order for further management of obesity A score of 1 indicates that a clinician followed all evidence of recommended obesity-related care; a score of 0 indicates that a clinician did not follow at least one recommendation for obesity-related care.
Time Frame
Baseline through 6 months after trial launch
Secondary Outcome Measure Information:
Title
Change in composite measure of clinician's adherence to clinical guidelines
Description
Change from baseline through 12 and 18 months in composite measure of adherence to clinical guidelines, calculated from practice behaviors queried from the electronic health record. A dichotomous variable, adherence is defined as whether or not, for each relevant visit, the clinician followed all evidence of recommended obesity-related care during the study period: Inclusion of diagnosis code indicating high BMI in visit diagnosis associated with the visit or as an active diagnosis in the problem list Recommended lab orders for obesity related comorbidities, if eligible Appropriate BP measurement in children 3 and older Counseling diagnosis codes or structured documentation (every visit) Follow-up visit requested at visit or active referral order for further management of obesity A score of 1 indicates that a clinician followed all evidence of recommended obesity-related care; a score of 0 indicates that a clinician did not follow at least one recommendation
Time Frame
Baseline through 18 months after trial launch
Title
Change in inclusion of diagnosis code indicating high BMI in problem list
Description
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of inclusion of diagnosis code indicating high BMI in problem list, queried from the electronic health record at baseline, 6, 12, and 18 months to see change at 6 months and how it's sustained at 12 and 18 months. A higher proportion of visits with relevant diagnosis code is consistent with recommended care.
Time Frame
Baseline through 18 months after trial launch
Title
Change in inclusion of diagnosis code indicating high BMI in visit diagnosis
Description
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of inclusion of diagnosis code indicating high BMI queried from the electronic health record. A higher proportion of visits with relevant diagnosis code is consistent with recommended care.
Time Frame
Baseline through 18 months after trial launch
Title
Change in adherence to guideline recommended screening lab orders for obesity related comorbidities, if eligible
Description
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of screening lab orders for obesity-related comorbidities recommended by the American Academy of Pediatrics clinical practice guideline for obesity based on age and BMI percentile, queried from the electronic health record. A higher proportion of visits with recommended screening lab orders is consistent with recommended care.
Time Frame
Baseline through 18 months after trial launch
Title
Change in appropriate blood pressure screening in children 3 and older
Description
Visits completed among children 3-18 years with BMI ≥85th percentile during the study period with evidence of appropriate blood pressure screening queried from the electronic health record. A higher proportion of visits with blood pressure screening is consistent with recommended care.
Time Frame
Baseline through 18 months after trial launch
Title
Change in structured documentation of counseling
Description
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of counseling structured documentation queried from the electronic health record. A higher proportion of visits with counseling structured documentation is consistent with recommended care.
Time Frame
Baseline through 18 months after trial launch
Title
Change in follow-up visit requested
Description
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of follow-up visit requested, queried from the electronic health record. A higher proportion of visits with follow-up visit requested is consistent with recommended care.
Time Frame
Baseline through 18 months after trial launch
Title
Change in referral for further management of obesity
Description
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of referral for further management of obesity queried from the electronic health record. A higher proportion of visits with follow-up or referral for further management of obesity is consistent with recommended care.
Time Frame
Baseline through 18 months after trial launch
Title
Change in weight loss medication orders, if eligible
Description
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of weight loss medication orders, if eligible, queried from the electronic health record. A higher proportion of visits with weight loss medication orders, when eligible, is consistent with recommended care.
Time Frame
Baseline through 18 months after trial post intervention launch
Title
Change in bariatric surgery program referrals, if eligible
Description
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of bariatric surgery program referrals, if eligible queried from the electronic health record. A higher proportion of referrals to bariatric surgery programs, when eligible, is consistent with recommended care.
Time Frame
Baseline through 18 months after trial launch
Title
Change in potentially unnecessary insulin or thyroid laboratory tests ordered
Description
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of insulin or thyroid lab orders, not routinely recommended for evaluation of children with obesity, queried from the electronic health record. A lower proportion indicates better adherence to recommended care.
Time Frame
Baseline through 18 months after trial launch
Title
Clinicians' utilization of the clinical decision support tools
Description
Visits completed among children 2-18 years with BMI ≥85th percentile during the study period with evidence of clinician use of the clinical decision support tools in the electronic health record developed for this trial, calculated from electronic health record query. Measure= % of visits at intervention sites at which the clinicians' uses clinical decision support tools through18 months A higher proportion indicates greater utilization of clinical decision support tools.
Time Frame
During the 18 months following trial launch
Title
Change in clinicians' attitudes and practice around managing elevated BMI in primary care
Description
Change in clinician's attitudes and practice around management of elevated BMI measured using survey questions; Possible responses range from 1 (strongly disagree) to 5 (strongly agree) for attitudes or 1 (never) to 5 (almost always).
Time Frame
Pre-intervention and 6 months post intervention launch
Title
Cost and cost-effectiveness of iPOP-UP
Description
Site-specific costs of implementing iPOP-UP per practice site and per patient incremental cost of iPOP-UP compared with usual care. Calculated based on study team logs, EHR data on healthcare utilization, and surveys of clinicians.
Time Frame
6 months before trial launch and up to 15 months after first primary care visit following trial launch

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Primary Care Practices: all primary care practices using the EHR system of one of the 3 health systems participating in the study that agree to participate in the iPOP-UP trial; Clinician-participants: all clinicians who delivery pediatric primary care at the participating practices, including physicians and physicians-in-training (residents and fellows), physician assistants (PA), nurse practitioners (NP)/advanced practice registered nurses (APRNs); Patient-participants: all patients ages 2-18 with overweight/obesity seen during the study period may be impacted by the intervention. A limited dataset will be collected for the subset of these 2 to 18 years old patients with BMI ≥ 85th percentile for age and sex seen for a well or follow-up visit during the study period in a primary care department and conducted by a prescribing clinician (physician, NP, PA) Exclusion Criteria: None - exclusion criteria are purposefully limited in this real-world implementation study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mahnoosh (Mona) Sharifi, MD, MPH
Phone
(203) 785-7821
Email
mona.sharifi@yale.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Emily B Finn, MPH
Email
e.finn@yale.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mahnoosh (Mona) Sharifi, MD, MPH
Organizational Affiliation
Yale University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Eskenazi Health
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Randall W Grout, MD
Email
rgrout@iu.edu
Facility Name
Duke University
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27708
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dean S Miner, MD
Email
dean.miner@duke.edu
First Name & Middle Initial & Last Name & Degree
Charles T Wood, MD, MPH
Email
charles.wood@duke.edu
Facility Name
Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jeremy J Michel, MD, MHS
Email
michelj@chop.edu

12. IPD Sharing Statement

Plan to Share IPD
No

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Dissemination and Implementation of Improving Pediatric Obesity Practice Using Prompts

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