Attention-deficit Hyperactivity, Disruptive Behavior, Oppositional Defiant Disorder
Conditions
Keywords
Emotional Behavioral Dyscontrol
Brief summary
The purpose of this study is to develop an innovative wearable tracking protocol that will use Artificial Intelligence (AI) technology to monitor sleep and behavior of 3-7 year old children.
Interventions
DEVICEGarmin
A smartwatch device that measures subjects level of activity, heartrate, respirations and quality of your sleep at night. Artificial intelligence will be applied to analyze all the data over the course of 12 weeks to monitor and attempt to predict the onset of tantrums or disruptive behavior. Subjects are required to wear the watch at least 70% of the day and night each day for 70% of days during 12 weeks of treatment.
Sponsors
Mayo Clinic
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
3 Years to 99 Years
Healthy volunteers
Yes
Inclusion criteria
- Children: * Ages 3-7. * Outpatients or Inpatients. * Any gender, race or ethnicity. * Able to provide developmentally appropriate informed assent, and legal guardians able to provide informed consent . * EBP Severity rated above the clinically significant range (≥120; T-score ≥ 60) (Eyberg Child Behavior Inventory- ECBI; Eyberg & Pincus, 1999). * Need for more intensive behavioral treatments such as ER visit for behavioral dyscontrol or hospitalization will not be exclusionary or exit criteria. * Families approached for participation will be asked to commit to complete the treatment. * At least one primary caregiver and the identified child will have to be able to speak and understand English.
Exclusion criteria
- Children: * Formal diagnosis of Severe Intellectual disability, Autistic Spectrum Disorder Level 3, or a psychotic disorder for the child. * Parents not consenting to the study. * Parents or child is not able to adhere to the study protocol. * A Child who is reasonable expected to be unable to tolerate wearing the Garmin device for at least 70% of the time during the day and night 70% of the days during the treatment (12 weeks). This is based on the principal investigator's discretion. * Unable to speak and understand English. * Refusal or withdrawal of consent, inability, or unwillingness to adhere to study procedures. * Children in foster care. Inclusion Criteria - Adults: * Agree to wear Garmin watch. * Ages 18-99. * Any gender, race, ethnicity. * Able to provide informed consent.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Frequency of Garmin use | 12 weeks | Number of days participants wear the Garmin smartwatch |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Eyberg Child Behavior Inventory | 12 weeks | The Eyberg Child Behavior Inventory questionnaire is measured on two subscales for a series of phrases that describe a children's behavior. The first subscale is for indicating the frequency of the behavior using a scale of 1= never to 7 = Always; the second subscale indicates yes = 1 or no = 0 for whether the behavior is currently a problem for them. Reponses are total with a higher score indicating greater severity of child's behavior. |
| Pediatric Sleep Questionnaire | 12 weeks | Pediatric Sleep Questionnaire to assess child's sleep with a series of 22 questions on a yes/no problem scale. |
Countries
United States
Outcome results
None listed