Ignite Creation Date:
2024-05-06 @ 3:36 PM
Last Modification Date:
2024-10-26 @ 1:52 PM
Study NCT ID:
NCT04682730
Status:
COMPLETED
Last Update Posted:
2023-07-12
First Post:
2020-12-16
Brief Title:
An Implementation Strategy for the Adoption of an Evidence-Based Guideline for Pit-and-Fissure Sealants
Sponsor:
University of Pittsburgh
Organization:
University of Pittsburgh
Study Overview
Official Title:
An Implementation Strategy for the Adoption of an Evidence-Based Guideline for Pit-and-Fissure Sealants Using a Framework From Organizational Development
Status:
COMPLETED
Status Verified Date:
2023-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
DISGO
Brief Summary:
The purpose of this implementation science study is to determine whether Deliberative Loops are effective in increasing providers adherence to the non-cavitated caries component of the American Dental Associations pit-and-fissure sealant evidence-based clinical practice guideline The investigators use a stepped wedge design to randomly assign dental clinics to the Deliberative Loop intervention In a Deliberative Loop stakeholders receive background information participate in a facilitated discussion and share their views with leadership The Deliberative Loop intervention is designed to help stakeholders form informed opinions in this study stakeholders will be forming informed opinions about the implementation interventions they think will increase their clinics adherence to the guideline The investigators hypothesize that compared with the pre-intervention period following the intervention providers will place or treatment plan sealants for significantly more occlusal non-cavitated carious lesions
Detailed Description:
The purpose of this implementation science study is to determine whether Deliberative Loops are effective in increasing providers adherence to the non-cavitated caries component of the American Dental Associations pit-and-fissure sealant evidence-based clinical practice guideline The investigators use a stepped wedge design to randomly assign dental clinics to the Deliberative Loop intervention In a Deliberative Loop stakeholders receive background information participate in a facilitated discussion and share their views with leadership The Deliberative Loop intervention is designed to help stakeholders form informed opinions in this study stakeholders will be forming informed opinions about the implementation interventions they think will increase their clinics adherence to the guideline The investigators hypothesize that compared with the pre-intervention period following the intervention providers will place or treatment plan sealants for significantly more occlusal non-cavitated carious lesions NCCL
All persons employed by Kaiser Permanente Northwest or Permanente Dental Associates and who work in a Kaiser Permanente Northwest dental clinic at any level eg part time full time will be eligible to participate in the study This includes both service providers and front-of-the-house staff approximately 1200 employees
This is a Stage III study
Participating sites include the 16 general dental clinics of Kaiser Permanente Northwest All clinics are located within the United States
The estimated time from when the study opens to enrollment until completion of data collection is 16 months It will take approximately one to two months for each individual participant to complete all study-related tasks depending on how soon after the introductory session the Deliberative session can be scheduled
All persons employed by Kaiser Permanente Northwest or Permanente Dental Associates and who work in a Kaiser Permanente Northwest dental clinic at any level eg part time full time will be eligible to participate in the study This includes both service providers and front-of-the-house staff approximately 1200 employees
This is a Stage III study
Participating sites include the 16 general dental clinics of Kaiser Permanente Northwest All clinics are located within the United States
The estimated time from when the study opens to enrollment until completion of data collection is 16 months It will take approximately one to two months for each individual participant to complete all study-related tasks depending on how soon after the introductory session the Deliberative session can be scheduled
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| U01DE027452 | NIH | None | None |
| 17-077-E | OTHER | NIDCR | httpsreporternihgovquickSearchU01DE027452 |