Clinical Trials Directory

Trials / Completed

CompletedNCT03873220

Monitoring Of Scratch Via Accelerometry In Children

Feasibility for Quantification of Scratch Behavior and Sleep in Children With Atopic Dermatitis

Status
Completed
Phase
Study type
Observational
Enrollment
62 (actual)
Sponsor
Boston University · Academic / Other
Sex
All
Age
2 Years – 11 Years
Healthy volunteers
Not accepted

Summary

Sleep sensors, wrist worn accelerometers, polysomnography (PSG), and associated data analysis platforms would provide quantitative and qualitative knowledge regarding the action of scratching and sleep quantity in a symptomatic atopic dermatitis (AD) population. The overall aim of this research is to validate the use of sensor technology and digital measures to quantitatively and qualitatively evaluate scratch and sleep in AD patients, and specifically in this study in children ages 2 to 11 years. To evaluate this experimental paradigm, the investigators propose using wearable accelerometers, a sleep sensor, PSG, videography and associated traditional patient-reported outcome measures/clinical outcome assessments (PRO/COA) in patients/caregivers with AD in a well-controlled in-laboratory and at-home study.

Detailed description

To assess the feasibility of quantifying scratch and sleep in children with Atopic Dermatitis (AD), children, age 2 to 11 years, with AD will be recruited. The subjects will complete specific questionnaires related to itch, sleeping habits and AD and continuously wear two wrist worn accelerometry devices. The EarlySense Sleep Monitor will also be placed underneath the mattress to measure additional sleep related activities. The study will be comprised of two overnight sleep laboratory site visits. The clinic visits will be followed by a continuous \~48 hour in-home environment assessment period (defined as the subject's daily routine environment). During the sleep lab site visit, the subject and accompanying parent(s)/guardian(s) will sleep overnight at the facility. The subject will be video-recorded during the in-sleep lab visit, wear the wrist accelerometry devices, use the sleep sensor and complete assessments (Depending on age, parent/guardian may complete some assessments). Upon the completion of sleep lab activities the subjects will then continue to wear the wrist accelerometry devices, utilize the sleep sensor and complete Patient Reported Outcome/Clinical Outcome Assessments (PRO/COA) assessments during the 48 hour in-home assessment. At the conclusion of the in-home portion of the assessment, the subject will return the device/s and assessments to the facility and undergo brief assessments/interview.

Conditions

Interventions

TypeNameDescription
DEVICEWrist Actigraphy DevicesA watch-like wearable sensor
DEVICESleep MonitorRemote Sensor
DEVICEPolysomnographySleep Monitor
DEVICEVideographyThermal Camera

Timeline

Start date
2018-12-14
Primary completion
2020-06-09
Completion
2020-06-09
First posted
2019-03-13
Last updated
2020-12-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03873220. Inclusion in this directory is not an endorsement.