- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT03862443
BEhavioral EConomics for Oral Health iNnovation Pilot Trial (BEECON Pilot)
1 mars 2019 uppdaterad av: 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.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
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.
Studietyp
Interventionell
Inskrivning (Faktisk)
36
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
California
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Santa Monica, California, Förenta staterna, 90405-1828
- Venice Family Clinic Children First Early Head Start
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
6 månader till 3 år (Barn)
Tar emot friska volontärer
Ja
Kön som är behöriga för studier
Allt
Beskrivning
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.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Förebyggande
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Dubbel
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
---|---|
Experimentell: 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.
|
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.
|
Experimentell: 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.
|
Inget ingripande: 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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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Mean number of qualifying half-day toothbrushing episodes per week
Tidsram: Baseline visit through the Month 2 visit
|
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.)
|
Baseline visit through the Month 2 visit
|
Proportion of parents/caregivers attending a dental visit
Tidsram: Month 2 visit
|
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.
|
Month 2 visit
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Proportion of weeks the parent/caregiver synced toothbrushing data with the app
Tidsram: Baseline visit through Month 2 visit
|
Proportion of weeks the parent/caregiver synced toothbrushing data with the app
|
Baseline visit through Month 2 visit
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Mean number of days per week with parent/caregiver-reported twice daily brushing
Tidsram: Baseline visit through the Month 2 visit
|
Twice daily brushing with fluoridated toothpaste, based on parent/caregiver-reported frequency diaries
|
Baseline visit through the Month 2 visit
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Fluoridated toothpaste use
Tidsram: 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
Tidsram: Month 2 visit
|
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).
|
Month 2 visit
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EHS site participation
Tidsram: 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
Tidsram: Month 0
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Willingness of EHS staff participation in assisting with recruitment
|
Month 0
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Proportion of parents/caregivers who consent
Tidsram: Baseline visit
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Willingness of parents/caregivers to provide informed consent and approve access to ChildPlus dental visit data
|
Baseline visit
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Proportion of parents/caregivers willing to be randomized
Tidsram: Baseline visit
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Willingness of parents/caregivers to be randomized to a study arm as part of the consenting process
|
Baseline visit
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Proportion of parents/caregivers adhering to study procedures
Tidsram: 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
Tidsram: 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
Tidsram: 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)
|
Baseline visit through the Month 2 visit
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Feasibility of measuring toothbrushing frequency with diaries
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: Baseline visit through Month 2 visit
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Willingness to use the smart powered toothbrush handle (percentage with any brushing data)
|
Baseline visit through Month 2 visit
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Comfort with smart powered toothbrush
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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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Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Samarbetspartners
Utredare
- Huvudutredare: James G Kahn, MD, MPH, University of California, San Francisco
Publikationer och användbara länkar
Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
10 maj 2017
Primärt slutförande (Faktisk)
13 augusti 2017
Avslutad studie (Faktisk)
19 mars 2018
Studieregistreringsdatum
Först inskickad
14 februari 2019
Först inskickad som uppfyllde QC-kriterierna
1 mars 2019
Första postat (Faktisk)
5 mars 2019
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
5 mars 2019
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
1 mars 2019
Senast verifierad
1 mars 2019
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 16-19968
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
NEJ
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
Studerar en amerikansk FDA-reglerad produktprodukt
Nej
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .
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