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- Klinische proef NCT03862443
BEhavioral EConomics for Oral Health iNnovation Pilot Trial (BEECON Pilot)
1 maart 2019 bijgewerkt door: University of California, San Francisco
Influence of Financial Incentives on Oral Disease Management in Young Children: A Randomized Pilot Trial
This Phase I randomized pilot trial will assess the efficacy of a fixed incentive payment program and drawing incentive payment program versus a control program to promote early childhood caries (ECC) preventive health behaviors (i.e., toothbrushing performance and dental visit attendance) for young children of predominantly Latino parents/caregivers enrolled in/waitlisted for Early Head Start (EHS) home visit programs.
Studie Overzicht
Toestand
Voltooid
Interventie / Behandeling
Gedetailleerde beschrijving
If both groups are acceptable and feasible, the reward group with toothbrushing outcomes at least 20% better than the other one (and the control) will be chosen for a future Phase II/III trial; if they are similar, the fixed monetary reward will be used because it is simpler to explain, monitor, and implement.
Studietype
Ingrijpend
Inschrijving (Werkelijk)
36
Fase
- Niet toepasbaar
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
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California
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Santa Monica, California, Verenigde Staten, 90405-1828
- Venice Family Clinic Children First Early Head Start
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
6 maanden tot 3 jaar (Kind)
Accepteert gezonde vrijwilligers
Ja
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
Inclusion Criteria for Parent/Caregiver:
- Provide signed and dated informed consent form in English or Spanish.
- Agree to comply with all study procedures and be available for the duration of the study visit.
- Male or female, aged 18 and older.
- Speak, read, and write either English or Spanish.
- Be a parent or caregiver of a child at least 6 months old but less than 3.5 years (42 months), with at least 2 fully erupted teeth and enrolled in, or waitlisted for, one of the three participating Los Angeles County EHS home visit programs.
- Not be planning to move residence for the next 6 months outside the greater Los Angeles area.
- Own a smartphone with the Google Play or iTunes store and be willing to download the smart powered TB app
- Be willing to be contacted via text-messaging (SMS) for study related notifications, such as incentives earned or reminders to sync the TB
Exclusion Criteria:
- Known allergic reaction to components of the study product(s).
- Uncooperative or behaviorally unsuited (assessed during a TB prophylaxis at the initial baseline study visit).
- A sibling of a child already enrolled in the study (the family's oldest child in the eligible age range will be the study child).
- Enrolled in foster care.
- Anything else that would place him/her at increased health risk or preclude the individual's full compliance with or completion of the study.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Preventie
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Dubbele
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: Fixed Incentive
Eligible to earn a weekly payment during the 2-month incentive intervention period.
Possible weekly winnings depend on toothbrushing performance collected through smart powered toothbrush synced to a smartphone app: low adherence threshold (brushing child's teeth once per day for 7 days in a week) will win $5; high adherence threshold (brushing twice per day for 14 days in a week) will win $10.
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The Fixed Incentive intervention is a fixed reward, in which participants are eligible for fixed weekly payments based on toothbrushing performance collected through smart powered toothbrush synced to a smartphone app.
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Experimenteel: Drawing Incentive
Eligible to earn a weekly drawing entry with different winning probabilities during the 2-month incentive intervention period.
Possible weekly winnings depend on toothbrushing performance collected through smart powered toothbrush synced to a smartphone app: low adherence threshold (brushing child's teeth once per day for 7 days in a week) will have an 18% chance of winning $25 and a 1% chance of winning $50 (expected $5 payout); high adherence threshold (brushing twice per day for 14 days in a week) will have a 34% chance of winning $25 and a 3% chance of winning $50 (expected $10 payout).
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The Drawing Incentive intervention is a drawing reward, in which participants are eligible for weekly payments based on toothbrushing performance collected through smart powered toothbrush synced to a smartphone app.
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Geen tussenkomst: Control - Delayed Incentive
No rewards during the first 2-months, but information on toothbrushing performance collected through smart powered toothbrush synced to a smartphone app.
After the Month 2 follow-up visit, may opt to participate in a delayed 2-month open label extension to earn the same monetary rewards the fixed incentive intervention group could earn Baseline through Month 2.
Not a formal part of this trial, but rather a necessary condition to assure all participating parents/caregivers have the chance to earn the same monetary incentives.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Mean number of qualifying half-day toothbrushing episodes per week
Tijdsspanne: Baseline visit through the Month 2 visit
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Mean number of qualifying half-day episodes per week in which a parent/caregiver brushes a child's teeth.
(A Bluetooth-recorded toothbrushing episode qualifies if it lasts at least one minute within one of 14 half-day windows in the week.)
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Baseline visit through the Month 2 visit
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Proportion of parents/caregivers attending a dental visit
Tijdsspanne: Month 2 visit
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In the subset of children at baseline with no dental visit in the EHS ChildPlus health module, whether or not the child has a ChildPlus documented dental visit at the two-month follow-up.
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Month 2 visit
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
---|---|---|
Proportion of weeks the parent/caregiver synced toothbrushing data with the app
Tijdsspanne: Baseline visit through Month 2 visit
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Proportion of weeks the parent/caregiver synced toothbrushing data with the app
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Baseline visit through Month 2 visit
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Mean number of days per week with parent/caregiver-reported twice daily brushing
Tijdsspanne: Baseline visit through the Month 2 visit
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Twice daily brushing with fluoridated toothpaste, based on parent/caregiver-reported frequency diaries
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Baseline visit through the Month 2 visit
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Fluoridated toothpaste use
Tijdsspanne: Baseline visit through the Month 2 visit
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Change in child toothpaste pump weight
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Baseline visit through the Month 2 visit
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Child plaque score
Tijdsspanne: Month 2 visit
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The child's Debris Index component (plaque score) of the Simplified Oral Hygiene Index (Greene and Vermillion) modified to include only maxillary incisor teeth after disclosing with plaque solution.
The scale (which is a mean value) range is 0 (no debris or stain) to 3 (soft debris covering more than two thirds of the exposed tooth surface).
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Month 2 visit
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EHS site participation
Tijdsspanne: Month 0
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Willingness of LA County EHS to sign memoranda of understanding
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Month 0
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EHS staff participation
Tijdsspanne: Month 0
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Willingness of EHS staff participation in assisting with recruitment
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Month 0
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Proportion of parents/caregivers who consent
Tijdsspanne: Baseline visit
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Willingness of parents/caregivers to provide informed consent and approve access to ChildPlus dental visit data
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Baseline visit
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Proportion of parents/caregivers willing to be randomized
Tijdsspanne: Baseline visit
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Willingness of parents/caregivers to be randomized to a study arm as part of the consenting process
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Baseline visit
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Proportion of parents/caregivers adhering to study procedures
Tijdsspanne: Baseline visit through the Month 2 visit
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Willingness of parents/caregivers to adhere to study procedures, including completing questionnaire instruments, bringing toothbrushing frequency diaries to 2-month follow-up visit, and bringing toothpaste pump to 2-month follow-up visit
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Baseline visit through the Month 2 visit
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Proportion of children who cooperate
Tijdsspanne: Baseline visit through the Month 2 visit
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Willingness of child to cooperate with study procedures, including dental screening, extraoral photo, and plaque assessment
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Baseline visit through the Month 2 visit
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Proportion of parents/caregivers willing to use the toothpaste pump
Tijdsspanne: Baseline visit through the Month 2 visit
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Willingness to use the toothpaste pump (percentage with any use and percentage change in pump weight)
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Baseline visit through the Month 2 visit
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Feasibility of measuring toothbrushing frequency with diaries
Tijdsspanne: Month 2 visit
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Bringing toothbrushing diaries to the follow-up visit and willingness to provide them to study staff
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Month 2 visit
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Feasibility of using toothpaste pump weight as a measure of usage
Tijdsspanne: Month 2 visit
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Bringing the toothpaste pump to the follow-up visit for weighing
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Month 2 visit
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Proportion of parents/caregivers willing to use the disclosing solution
Tijdsspanne: Baseline visit and Month 2 visit
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Willingness of children to comply with the plaque disclosing procedure
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Baseline visit and Month 2 visit
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Proportion of parents/caregivers willing to use photographs for central assessment
Tijdsspanne: Baseline visit and Month 2 visit
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Willingness of the child to allow photographs, the ability to transmit the photographs securely, and the ability of the central clinician to score them reliably and confidently
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Baseline visit and Month 2 visit
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Proportion of parents/caregivers willing to use smart powered toothbrush
Tijdsspanne: Baseline visit through Month 2 visit
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Willingness to use the smart powered toothbrush handle (percentage with any brushing data)
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Baseline visit through Month 2 visit
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Comfort with smart powered toothbrush
Tijdsspanne: Baseline visit through Month 2 visit
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Child and parent comfort level with using the smart powered toothbrush
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Baseline visit through Month 2 visit
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Proportion of parents/caregivers willing to use smartphone app
Tijdsspanne: Baseline visit
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Willingness to download the smartphone app and keep it for the duration of the study
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Baseline visit
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Proportion of parents/caregivers willing to receive text messages
Tijdsspanne: Baseline visit
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Willingness to be contacted with study-related text messages each week during the intervention period
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Baseline visit
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Feasibility of syncing toothbrush to app
Tijdsspanne: Baseline visit
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Successfully synced the toothbrush to app during baseline visit
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Baseline visit
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Medewerkers
Onderzoekers
- Hoofdonderzoeker: James G Kahn, MD, MPH, University of California, San Francisco
Publicaties en nuttige links
De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
10 mei 2017
Primaire voltooiing (Werkelijk)
13 augustus 2017
Studie voltooiing (Werkelijk)
19 maart 2018
Studieregistratiedata
Eerst ingediend
14 februari 2019
Eerst ingediend dat voldeed aan de QC-criteria
1 maart 2019
Eerst geplaatst (Werkelijk)
5 maart 2019
Updates van studierecords
Laatste update geplaatst (Werkelijk)
5 maart 2019
Laatste update ingediend die voldeed aan QC-criteria
1 maart 2019
Laatst geverifieerd
1 maart 2019
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 16-19968
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
NEE
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .
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