- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02077985
Sensory Adapted Dental Environment to Enhance Oral Care for Children With ASD (SADE)
Sensory Adapted Dental Environment to Enhance Oral Care for Children With Autism
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The goal of this R34 NIDCR Planning and Pilot Data Grant is to collect information to support a later clinical trial on the effectiveness of a specially adapted dental environment for children who have difficulty tolerating oral care in the dental clinic. Within this project, two groups of children were studied: children with autism spectrum disorders (ASD) and typically developing children, including those who are over-reactive to sensory stimulation. Commonly, such children exhibit anxiety and negative behavioral reactions when confronted with experiential aspects of dental visits such as exposure to bright fluorescent lighting, touch in or around the mouth, or the texture and smell of various oral care products. We pilot tested a sensory adapted dental environment (SADE) to examine its effect on reducing anxiety and behavioral problems among the targeted groups of children. The SADE intervention includes such adaptations as dimmed lighting, exposure to soothing music, and application of a special vest which provides deep pressure sensations that are calming. If our preliminary assessment produces promising results, we will later more comprehensively test the intervention in a full-scale randomized clinical trial, which will be supported by a U01 award.
The specific aims of the R34 grant are to promote the ability to conduct the future trial by:
- Developing a manual for the SADE intervention and assessing the intervention's feasibility.
- Collecting preliminary data on the intervention's effectiveness and potential cost-savings.
- Pilot testing the recruitment strategy and assessment battery that will be used in the anticipated trial.
- Developing the system of documents and data management for the future trial.
- Generating the proposal for the U01 award to conduct the planned trial.
Research participants were 45 ethnically diverse children aged 6-12 years, 22 with ASD and 23 who are typically developing. Each child underwent two dental cleanings four months apart: dental cleaning in a standard dental environment and dental cleaning in the sensory adapted environment. For each group of children (i.e., ASD and typically developing), these two conditions were compared in their effects on anxiety and negative behavioral reactions, as measured by videotape coding, psychophysiological indices, and various rating scales.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Diagnosis of autism using ADOS (or) typically developing
- age 6 to 12
- parents speak English or Spanish
- in need of an oral cleaning (no previous cleaning within past four months)
Exclusion Criteria:
- disability such as cleft palate, significant motor impairment (e.g cerebral palsy), no genetic, endocrine, or metabolic dysfunction that would interfere with oral care or EDA.
Additional exclusion for participants in Typical Group include
- diagnosis of ASD or other DD
- diagnosis of ADHD, anxiety disorder, bipolar disorder
- siblings not diagnosed with ASD
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: Regular Dental Environment
There are two dental environments - the regular dental environment and the sensory dental environment; each child will be randomized to which is first.
In the Regular dental environment no sensory characteristics of the dental environment are altered, the cleaning is conducted as per usual.
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Experimental: Sensory Adapted Dental Environment
There are two dental environments - the regular dental environment and the sensory dental environment; each child will be randomized to which is first.
In the Sensory Adapted Dental Environment the sensory characteristics of the dental environment are altered (visual, auditory, tactile adaptations).
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See study arm description.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Electrodermal activity (EDA)
Time Frame: Recorded continuously for three minutes prior to cleaning, through duration of cleaning (approximately 10-45 minutes), and for three minutes at end of cleaning for each dental cleaning.
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Electrodermal activity (EDA) is a non-invasive measure of the ability of the skin to conduct an electrical current, which increases when the sympathetic "fight or flight" nervous system is activated during times of stress.
EDA was analyzed in two ways in this study to investigate physiological stress/anxiety: (1) tonic skin conductance level (SCL) and (2) frequency of non-specific skin conductance responses (NS-SCR).
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Recorded continuously for three minutes prior to cleaning, through duration of cleaning (approximately 10-45 minutes), and for three minutes at end of cleaning for each dental cleaning.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Children's Dental Behavioral Rating Scale (CDBRS)
Time Frame: Videorecorded throughout dental cleaning (approximately 10-45 minutes); coded during first five minutes of dental prophylaxis.
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The Children's Dental Behavioral Rating Scale (CDBRS) evaluates overt distress behaviors exhibited by children in the dental office.
The child's behavior is videotaped during the dental cleaning; the first five minutes of prophylaxis are coded from the video data at a later date.
Coding included marking the presence or absence of three distress behaviors (mouth movement, head movement, forehead movement) and the presence or absence and the severity of two distress behaviors (whimper/cry/scream, verbal stall or delay) during each one-minute interval of the five minute video.
Significant inter-rater reliability by two trained raters on a sample of children with and without ASD was obtained.
The raw score (0-45) was converted, via Rasch analysis, to a scale score of 1-100.
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Videorecorded throughout dental cleaning (approximately 10-45 minutes); coded during first five minutes of dental prophylaxis.
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Number of hands used to restrain child
Time Frame: Recorded throughout the dental cleaning (approximately 10-45 minutes)
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The number of hands required to restrain the child during the dental cleaning experience was also utilized as a measure of uncooperative behavior.
This variable was recorded on researcher notes during the dental cleaning and was verified using the videotape of the dental cleaning.
Scoring included presence/absence as well as the number of hands used for restraint purposes during the cleaning.
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Recorded throughout the dental cleaning (approximately 10-45 minutes)
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Frankl Scale
Time Frame: Completed at the end of each dental cleaning (approximately 10-45 minutes)
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The Frankl Scale was completed by the dentist following the dental cleaning.
This one-item Likert Scale ranges from 1 (definitely negative) to 2 (negative) to 3 (positive) to 4 (definitely positive).
This assessment has high inter-rater reliability and moderate validity and has been used to measure the behavior of children with ASD.
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Completed at the end of each dental cleaning (approximately 10-45 minutes)
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The Anxiety and Cooperation Scale (A & C Scale)
Time Frame: Completed at the end of each dental cleaning (approximately 10-45 minutes)
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The Anxiety and Cooperation Scale (A & C Scale) has been shown to assess children's anxiety, fear, and cooperation as rated by dentists, and has good established reliability and validity.
Following a routine dental cleaning, the dentist rated overall patient behavior during treatment using a one-item Likert scale ranging from 0 (relaxed, smiling, demonstrates desired behavior, complies with demands) to 5 (out of control, loud crying, reverts to primitive flight responses, physical restraint required).
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Completed at the end of each dental cleaning (approximately 10-45 minutes)
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Time
Time Frame: Time from beginning to end of dental cleaning (approximately 10-45 minutes); recorded for each visit
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The length of time to complete the dental cleaning.
Used for cost-analysis of the intervention.
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Time from beginning to end of dental cleaning (approximately 10-45 minutes); recorded for each visit
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Sharon A Cermak, EdD, University of Southern California
Publications and helpful links
General Publications
- Chaspari T, Tsiartas A, Stein Duker LI, Cermak SA, Narayanan SS. EDA-gram: designing electrodermal activity fingerprints for visualization and feature extraction. Annu Int Conf IEEE Eng Med Biol Soc. 2016 Aug;2016:403-406. doi: 10.1109/EMBC.2016.7590725.
- Cermak SA, Stein Duker LI, Williams ME, Dawson ME, Lane CJ, Polido JC. Sensory Adapted Dental Environments to Enhance Oral Care for Children with Autism Spectrum Disorders: A Randomized Controlled Pilot Study. J Autism Dev Disord. 2015 Sep;45(9):2876-88. doi: 10.1007/s10803-015-2450-5.
- Cermak SA, Stein Duker LI, Williams ME, Lane CJ, Dawson ME, Borreson AE, Polido JC. Feasibility of a sensory-adapted dental environment for children with autism. Am J Occup Ther. 2015 May-Jun;69(3):6903220020p1-10. doi: 10.5014/ajot.2015.013714.
- Chaspari T, Tsiartas A, Stein LI, Cermak SA, Narayanan SS. Sparse representation of electrodermal activity with knowledge-driven dictionaries. IEEE Trans Biomed Eng. 2015 Mar;62(3):960-71. doi: 10.1109/TBME.2014.2376960. Epub 2014 Dec 4.
- Stein LI, Lane CJ, Williams ME, Dawson ME, Polido JC, Cermak SA. Physiological and behavioral stress and anxiety in children with autism spectrum disorders during routine oral care. Biomed Res Int. 2014;2014:694876. doi: 10.1155/2014/694876. Epub 2014 Jul 10.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 5R34DE022263-02 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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