Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
58 participants
INTERVENTIONAL
2018-10-01
2020-10-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Traditional OHI (Control)
Advice giving method of OHI known as "tell-show-do" to inform, demonstrate, and expect patient compliance.
No interventions assigned to this group
BMI (Test)
A derivative of motivational interviewing (MI), which is a patient-centered, collaborative counseling approach to strengthen an individual's intrinsic motivation towards a positive behavior change. BMI is intended for healthcare providers with limited time (5-10 minutes) to support a positive behavior change.
BMI
A derivative of motivational interviewing (MI), which is a patient-centered, collaborative counseling approach to strengthen an individual's intrinsic motivation towards a positive behavior change. BMI is intended for healthcare providers with limited time (5-10 minutes) to support a positive behavior change.
Interventions
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BMI
A derivative of motivational interviewing (MI), which is a patient-centered, collaborative counseling approach to strengthen an individual's intrinsic motivation towards a positive behavior change. BMI is intended for healthcare providers with limited time (5-10 minutes) to support a positive behavior change.
Eligibility Criteria
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Inclusion Criteria
* ≥ 18 years old
* Periodontal maintenance phase (at least one year)
* Plaque score ≥30% (O'Leary plaque score)
* Minimum of two sites with BOP
* Willingness to fulfill all study requirements
* Patient of Record at the University of Minnesota School of Dentistry
Exclusion Criteria
* Pregnant, planning to become pregnant, or unsure of pregnancy status (self-reported)
* Uncontrolled diabetes (HbA1C \> 7)
* Medical conditions that may influence the outcome of the study (neurologic or psychiatric disorders, systemic infections, cancer, and/or HIV/AIDS)
* Current use of oral bisphosphonates
* History of IV bisphosphonates
* Require pre-medication or on long-term antibiotics
* Current orthodontic treatment or planning to begin orthodontic treatment during the study
* Unable to comply with the study protocol
18 Years
ALL
Yes
Sponsors
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University of Minnesota
OTHER
Responsible Party
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Principal Investigators
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Michelle Arnett, MS
Role: PRINCIPAL_INVESTIGATOR
University of Minnesota
Locations
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School of Dentistry
Minneapolis, Minnesota, United States
Countries
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Other Identifiers
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DENT-2018-26921
Identifier Type: -
Identifier Source: org_study_id
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