The goal of this clinical trial is to test whether the autism-friendly app improves toothbrushing outcomes compared to a control app with only a digital mirror and countdown timer among children and teens (ages 8-17 years) with autism. The main questions it aims to answer are: 1. Will toothbrushing distribution, duration, and frequency be greater in the experimental arm than in the control arm? 2. Will toothbrushing habit formation be higher in the experimental arm than in the control arm? 3. Is caregiver and child self-efficacy a mediator of toothbrushing habit formation? 4. Do children who exhibit habit formation report better oral health-related quality of life? Participants will: 1. Use either the autism-friendly app or the control app during their daily toothbrushing routine for 3 months. 2. Complete surveys and assessments about toothbrushing behaviors and oral health over the course of the study.
The UH3 RCT will be conducted over four years. We will obtain a list of eligible participants from the main study recruitment site (Seattle Children's Hospital). We will obtain a list of individuals who express interest in participating in the study from other recruitment sites. UW staff will contact potential participants, describe the study, verify interest and screen for eligibility, and obtain informed consent and assent. The caregiver and their child/teen, aged 8-17 years, will be enrolled (N=270) as dyads and randomly assigned (1:1) to an experimental or control arm, accounting for sex and autism severity. The study participation will span one year. The participants in both arms will follow the same procedures. After enrollment, caregivers from both control and experimental groups will complete all surveys according to the determined schedules. Caregivers will complete a demographics survey and a toothpaste survey via phone. Caregivers will also complete an online survey, Social Responsiveness Scale-2 (SRS-2), via WPS Publishing, to provide data on the user's autism severity. Before the app use, caregivers will be asked to complete a 9-item Oral Health Behavior Survey (OHBS), 30-item Behavioral Survey (BS) and 38-item Short Sensory Profile (SSP) via REDCap at baseline. Caregivers will then be given a unique link to install a modified Brush Up/Brush Down app, depending on their assignment in the experimental or control arm respectively. The Brush Up app (experimental) features a cartoon character that helps guide the child through toothbrushing with a catchy song. It also includes a digital mirror where the child can watch themselves brush and a matching game where they earn stars by matching their toothbrushing movements with the character. The Brush Down app (control) includes only a digital screen mirror and a timer. We will ask the user to use the app twice a day for 3 months. The app will record the user's toothbrushing sessions. Users will be made aware of this during consent/assent process. The 9-item OHBS will be re-administered at 1 month, 2 months and 3 months of app use via REDCap. The 30-item BS will be re-administered at 2 weeks, 1 month, 2 months, and 3 months of app use via REDCap. Study staff will recruit 60 dyads (N=30 from each arm) for a post-trial debriefing interview lasting about 60 minutes using a semi-structured interview script to elicit responses about the experiences of using the app, the effects of the app on their child's long-term toothbrushing habit formation as well as ways the intervention could be further strengthened in the future to meet the needs of individuals with autism. The interviews will be audio recorded, transcribed, and verified for accuracy, and coded deductively using standard methods. After 3 months of app use, the caregivers will be asked to complete a 6-item BS, an abridged version of a 30-item BS, to assess long-term habit formation and oral health quality of life from months 4 to 12 of participation via REDCap. Study staff will reach out to the dyads who participated in post-trial interviews to obtain feedback on their experiences of using the app. The interviews will be audio recorded, transcribed, and verified for accuracy, and coded deductively using standard methods.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
270
The Brush Up app is an autism-friendly mobile app modified to improve toothbrushing skills and habits in children with autism spectrum disorder and includes a health education module, a cartoon role model, toothbrushing instructional song, digital screen mirror, and customizable app features.
The Brush Down app provides health education module, a digital screen mirror and a countdown timer. This app does not include autism-friendly features.
University of Washington School of Dentistry
Seattle, Washington, United States
Toothbrushing distribution
The primary outcome being measured is toothbrushing distribution. Toothbrushing distribution refers to the mean proportion of different tooth surfaces in the mouth that should be brushed during each toothbrushing episode (i.e., lingual, buccal occlusal). For each subject, one toothbrushing episode per day will be randomly sampled during week 12 to measure distribution.
Time frame: The primary outcome will be measured based on data from week 12 of the 3-month trial.
Toothbrushing duration
Toothbrushing duration refers to the mean number of seconds brushed per toothbrushing episode. For each subject, one toothbrushing episode per day will be randomly sampled during week12 to measure this outcome. For each sampled episode, the duration will be measured in seconds from the time toothbrushing commences until toothbrushing concludes. Idle time, which is defined as time not spent actively brushing during an episode will also be measured in seconds.
Time frame: The secondary outcome will be measured based on data from week 12 of the 3-month trial.
Toothbrushing Frequency
Toothbrushing frequency refers to the number of days the app was used at least twice per day. Timestamps will be recorded for each instance of toothbrushing with the app, which will be used to determine the number of days for measuring frequency.
Time frame: The secondary outcome will be measured based on data from week 12 of the 3-month trial.
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