Coordinated Oral Health Promotion (CO-OP) Chicago

NCT ID: NCT03397589

Last Updated: 2022-10-18

Study Results

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

420 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-01-20

Study Completion Date

2020-08-20

Brief Summary

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This study assesses the impact of oral health promotion delivered by community health workers in medical clinics, Women, Infants and Children (WIC) centers, and family homes. Investigators will assess oral health behaviors in children aged 0 to 3.

Detailed Description

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Dental caries is the most common chronic disease of childhood; an estimated 28% of children nationally aged 5 years and below have untreated dental disease. Pediatric dental caries are associated with pain, more severe infections, malnutrition, speech difficulties, poor school performance, cosmetic problems, and an overall lower quality of life. Similar to other chronic diseases, oral health disparities are seen with higher caries prevalence and worse outcomes in children from low income urban families and in children of African American and Latino ethnicity. These disparities have been demonstrated locally in Chicago. Many interventions have been implemented to attempt to reverse these disparities. Some involve public policy (fluorinated water), some are educational campaigns targeting individuals, while others focus on providing increased education and services through primary healthcare providers. Many of these programs have demonstrated efficacy but the disparities in oral health persist. The investigators propose this is because the interventions to date do not target the family as a whole and also have not targeted multiple levels simultaneously.

COordinated Oral health Promotion (CO-OP) Chicago brings together a team of clinical pediatricians and dentists, health researchers, and policy experts to rigorously test the ability of multiple oral health promotion interventions, both alone and in combination, to improve child and family oral health. The primary intervention is family-focused education and support from community health workers (CHWs). CO-OP Chicago will test the impact of a family-focused CHW intervention for oral health promotion when applied in clinical, community, and home settings. The primary study objective is to evaluate the efficacy of a one-year oral health CHW intervention, compared to usual care, to improve self-reported brushing frequency and observed plaque score in low income urban children under the age of 3 years old. The study's exploratory aim is to determine if the oral health CHW intervention impact on child tooth brushing behaviors varies when the CHWs are based out of a medical clinic compared to a community WIC center.

Conditions

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Dental Caries in Children Health Behavior Healthcare Disparities

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

cluster-randomized two arm trial with wait list control
Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Outcome Assessors
Because of the nature of the intervention, participants will know after randomization which arm they are in. Outcomes assessors and data analysts will be masked to study arm. Most investigators will be masked to study arm.

Study Groups

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CHW Arm

The intervention is community health worker (CHW) services. CHWs trained in oral health will be assigned to half of the sites. Participants in these sites will be offered four in-person visits and follow-up phone calls over 12-months. These visits can occur at the location of the family's preference (recruitment site, home, or mutually-agreed upon other location). A core curriculum of oral health topics will be covered during visits, with an emphasis on developing and sustaining healthy oral health management routines for the entire family.

Group Type EXPERIMENTAL

Community Health Worker (CHW) services

Intervention Type BEHAVIORAL

CHWs are non-clinical people who provide education, care coordination, and support to families.

Wait-list Control Arm

This arm will receive usual care. After completion of the final data collection at one year, participants and sites allotted to this arm will be offered CHW services.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Community Health Worker (CHW) services

CHWs are non-clinical people who provide education, care coordination, and support to families.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

Caregiver:

* Provide a signed and dated informed consent form
* Age 18 or older
* Be the primary caregiver of a child age 6-36 months old. The primary caregiver is defined for this study as the person (or one of the people) who is consistently responsible for the child's daily routines and who is a legal guardian.
* If a child lives in multiple households, the caregiver must live with the child at least 5 days of the week.
* The child must be an active patient/client in the clinic/center where recruited.
* Speak English or Spanish
* Willing to comply with all study procedures and be available for the duration of the study

Child:

* Age 6-36 months old
* An active patient/client in the clinic/center where recruited
* A minimum of two fully erupted central maxillary incisors

Exclusion Criteria

* Child with medical condition that limits his or her ability to conduct the study activities (such as severe developmental or cognitive delay, ventilator or oxygen dependence, oral aversion, severe facial deformities)
* Anything that would place the individual at increased risk or preclude the individual's full compliance with or completion of the study
* Anything that would place the research or intervention staff at increased risk
Minimum Eligible Age

6 Months

Maximum Eligible Age

36 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute of Dental and Craniofacial Research (NIDCR)

NIH

Sponsor Role collaborator

University of Illinois at Chicago

OTHER

Sponsor Role lead

Responsible Party

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Molly A. Martin

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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CEDA WIC Center Blue Island

Blue Island, Illinois, United States

Site Status

Chicago Department of Public Health WIC Centers (Greater Lawn Health Center, Friend Family Health Center, Westside Health Partnership)

Chicago, Illinois, United States

Site Status

Mile Square Health Center (Main, Englewood, Cicero, South Shore, Back of the Yards)

Chicago, Illinois, United States

Site Status

University of Illinois at Chicago Outpatient Care Center

Chicago, Illinois, United States

Site Status

Aunt Martha's Southeast Side Community Health Center

Chicago, Illinois, United States

Site Status

Vida Pediatrics

Chicago, Illinois, United States

Site Status

CEDA WIC Centers (Diversey, Irving Park)

Chicago, Illinois, United States

Site Status

Aunt Martha's Pediatric Health & Wellness Center

Chicago Heights, Illinois, United States

Site Status

CEDA WIC Center Harvey

Harvey, Illinois, United States

Site Status

CEDA WIC Center Maywood

Maywood, Illinois, United States

Site Status

CEDA WIC Oak Park

Oak Park, Illinois, United States

Site Status

Aunt Martha's South Holland Community Health Center

South Holland, Illinois, United States

Site Status

CEDA WIC Summit

Summit, Illinois, United States

Site Status

Countries

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United States

References

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Martin MA, Avenetti D, Lee HH, Nordgren R, Berbaum ML, Edomwande Y, Cui L, Sandoval A. Community health worker intervention to improve tooth brushing in young children: Results from a cluster randomized controlled trial. Community Dent Oral Epidemiol. 2023 Jun;51(3):503-511. doi: 10.1111/cdoe.12768. Epub 2022 Jun 29.

Reference Type DERIVED
PMID: 35766288 (View on PubMed)

Martin MA, Zimmerman LJ, Rosales GF, Lee HH, Songthangtham N, Pugach O, Sandoval AS, Avenetti D, Alvarez G, Gansky SA. Design and sample characteristics of COordinated Oral health Promotion (CO-OP) Chicago: A cluster-randomized controlled trial. Contemp Clin Trials. 2020 May;92:105919. doi: 10.1016/j.cct.2019.105919. Epub 2019 Dec 30.

Reference Type DERIVED
PMID: 31899372 (View on PubMed)

Provided Documents

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Document Type: Study Protocol, Statistical Analysis Plan, and Informed Consent Form

View Document

Other Identifiers

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UH3DE025483

Identifier Type: NIH

Identifier Source: secondary_id

View Link

2017-1090

Identifier Type: -

Identifier Source: org_study_id

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