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Completed No phase listed Observational Accepts healthy volunteers

Evaluation of a Bright Futures Oral Health Intervention

ClinicalTrials.gov ID: NCT01406366

Public ClinicalTrials.gov record NCT01406366. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

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Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Evaluation of a Bright Futures Oral Health Intervention for Pediatric Residents

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Pediatricians serve an important role in promoting health in families. Bright Futures offers a child and family-centered approach to health promotion in incorporating partnership and communication skills of providers. Two areas of importance are in promotion of oral health and prevention of iron deficiency. We plan to study implementing educational curriculum to pediatric residents through a randomized controlled trial. Randomization will be done through assignment at the level of pediatric training program. Residents randomized to Group 1 will receive education about Bright Futures partnership and communication skills with oral health as the main health promotion topic. Group 2 will receive educational curriculum pertaining to the topic of iron deficiency prevention. While pediatricians are positioned perfectly to partner and effectively communicate with families on these two issues, there are gaps in pediatric education addressing these topics. The CORNET continuity practices of the Ambulatory Pediatric Association provide a venue through which multiple residency programs that educate pediatric residents and whose residents provide medical care to underserved children can participate. The research hypotheses include: 1. Residents in Group 1 will have greater confidence, knowledge and competence in partnership building and communication with families 2. Residents in Group 1 will have greater knowledge and competence in discussing oral health promotion 3. Residents in Group 2 will have greater knowledge and competence in discussing iron deficiency prevention 4. Parent-child dyads in Group 1 will be more likely to have established a dental home 5. Parent-child dyads in Group 1 will be more likely to be satisfied with their healthcare encounter. Pediatric practices provide fertile ground for the provision of health promotion on oral health and iron deficiency prevention. However, evidence for the effectiveness of primary care clinician interventions of screening, referral and counseling to prevent dental caries is lacking \[14\]. The National Survey of America's Families \[15\] found 47% of children did not receive the recommended number of dental visits, with the youngest ones being least likely to receive any dental care. Although 90% of pediatricians agreed they had important roles in identifying and counseling patients on prevention of caries, half stated they had received no previous training during medical school or residency and their knowledge of basic oral health topics was limited \[13\]. These studies highlight that pediatricians play important roles in oral health and are capable of being trained to complete oral screening exams, but more education and guidance is needed. Iron deficiency is the most common childhood nutritional deficiency in the United States. Recent prevalence data have determined that 7-30% of children in the United States aged 1-2 years have iron deficiency and 3-10% have iron deficiency anemia \[17, 18\]. Specific goals in Health People 2010 include a reduction of iron deficiency to 5% in children less than 3 years of age.

Study identification

NCT ID
NCT01406366
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Continuity Research Network
Network
Enrollment
27 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Months to 35 Months
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 31, 2005
Primary completion
Nov 30, 2010
Completion
Nov 30, 2010
Last update posted
Jul 31, 2011

2005 – 2010

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
Dartmouth Hitchcock Medical Center Hanover New Hampshire 03755

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01406366, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 31, 2011 · Synced Sep 6, 2026

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