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Optimizing a Mobile Health Platform for Sleep Promotion and Obesity Prevention in Children

Primary Purpose

Insufficient Sleep, Obesity

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Fixed sleep goal
Personalized sleep goal
Digital sleep health messaging without virtual study visit
Digital sleep health messaging with virtual study visit
Inactive Parent-Directed Loss-Framed Incentive
Active Parent-Directed Loss-Framed Incentive
Inactive Supportive Feedback
Active Supportive Feedback
Sponsored by
Children's Hospital of Philadelphia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Insufficient Sleep focused on measuring insufficient sleep, obesity

Eligibility Criteria

8 Years - 12 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Aged 8-12 years olds. Insufficient sleep duration (<8.5 hours per night). Body mass index (BMI) between the 50th and 95th percentile for age and sex. One child per family. Exclusion Criteria: Diagnosed with a chronic disease. Diagnosed with a behavioral health problem. Diagnosed with a condition that can impact sleep or growth. Diagnosed with a condition affecting physical growth and maturation or dietary intake. Children with a history of cancer, kidney, GI, musculoskeletal, or sleep disorders. Children who will transition to high-school during the study. Children using steroids/hormones. Children regularly taking medications

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm 5

    Arm 6

    Arm 7

    Arm 8

    Arm 9

    Arm 10

    Arm 11

    Arm 12

    Arm 13

    Arm 14

    Arm 15

    Arm 16

    Arm Type

    Active Comparator

    Active Comparator

    Active Comparator

    Active Comparator

    Active Comparator

    Active Comparator

    Active Comparator

    Active Comparator

    Active Comparator

    Active Comparator

    Active Comparator

    Active Comparator

    Active Comparator

    Active Comparator

    Active Comparator

    Experimental

    Arm Label

    Condition 1

    Condition 2

    Condition 3

    Condition 4

    Condition 5

    Condition 6

    Condition 7

    Condition 8

    Condition 9

    Condition 10

    Condition 11

    Condition 12

    Condition 13

    Condition 14

    Condition 15

    Condition 16

    Arm Description

    Fixed guideline-based sleep goal, Digital sleep health messaging without virtual study visit consultation, Inactive caregiver-directed loss-framed incentive, Inactive supportive feedback.

    Fixed guideline-based sleep goal, Digital sleep health messaging without virtual study visit consultation, Inactive caregiver-directed loss-framed incentive, Active supportive feedback.

    Fixed guideline-based sleep goal, Digital sleep health messaging without virtual study visit consultation, Active caregiver-directed loss-framed incentive, Inactive supportive feedback.

    Fixed guideline-based sleep goal, Digital sleep health messaging without virtual study visit consultation, Active caregiver-directed loss-framed incentive, Active supportive feedback.

    Fixed guideline-based sleep goal, Digital sleep health messaging with virtual study visit consultation, Inactive caregiver-directed loss-framed incentive, Inactive supportive feedback.

    Fixed guideline-based sleep goal, Digital sleep health messaging with virtual study visit consultation, Inactive caregiver-directed loss-framed incentive, Active supportive feedback.

    Fixed guideline-based sleep goal, Digital sleep health messaging with virtual study visit consultation, Active caregiver-directed loss-framed incentive, Inactive supportive feedback.

    Fixed guideline-based sleep goal, Digital sleep health messaging with virtual study visit consultation, Active caregiver-directed loss-framed incentive, Active supportive feedback.

    Personalized sleep goal, Digital sleep health messaging without virtual study visit consultation, Inactive caregiver-directed loss-framed incentive, Inactive supportive feedback.

    Personalized sleep goal, Digital sleep health messaging without virtual study visit consultation, Inactive caregiver-directed loss-framed incentive, Active supportive feedback.

    Personalized sleep goal, Digital sleep health messaging without virtual study visit consultation, Active caregiver-directed loss-framed incentive, Inactive supportive feedback.

    Personalized sleep goal, Digital sleep health messaging without virtual study visit consultation, Active caregiver-directed loss-framed incentive, Active supportive feedback.

    Personalized sleep goal, Digital sleep health messaging with virtual study visit consultation, Inactive caregiver-directed loss-framed incentive, Inactive supportive feedback.

    Personalized sleep goal, Digital sleep health messaging with virtual study visit consultation, Inactive caregiver-directed loss-framed incentive, Active supportive feedback.

    Personalized sleep goal, Digital sleep health messaging with virtual study visit consultation, Active caregiver-directed loss-framed incentive, Inactive supportive feedback.

    Core intervention, Sleep goal, Sleep guidance messaging, Caregiver-directed loss-framed incentive, Supportive feedback.

    Outcomes

    Primary Outcome Measures

    Change in sleep duration
    The primary outcome for aims 1 and 3 is change in nighttime sleep duration (hours per night) on weeknights measured by a sleep tracker with high sensitivity and moderate specificity for measuring sleep.
    Change in fat mass index Z-score
    Aim 2 primary outcome. Total body fat mass will be measured by DXA. Fat mass index (FMI, kg of fat divided by height in meters squared) will be calculated, and age and gender specific FMI Z-scores will be determined using U.S. specific FMI growth charts.

    Secondary Outcome Measures

    Change in sleep onset
    Change in sleep onset (time subject falls asleep). Weeknights and weekends will be measured separately.
    Change in sleep offset
    Change in sleep offset (time subject wakes up). Weeknights and weekends will be measured separately.
    Change in sleep midpoint
    Change in sleep midpoint. Weeknights and weekends will be measured separately.
    Change in social jetlag
    Investigators will calculate "social jetlag" by subtracting the weekend night sleep midpoint from the weeknight sleep midpoint. Social jetlag provides an indication of the discrepancy between internal biological clocks and social requirements and has been linked to cardiometabolic risk.
    Change in sleep efficiency
    Change in sleep efficiency (percentage of time spent asleep during overnight sleep periods). Weeknights and weekends will be measured separately.
    Change in sleep onset latency
    Change in sleep onset latency (time to fall asleep). Weeknights and weekends will be measured separately.
    Change in wake after sleep onset
    Change in wake after sleep onset (time awake during overnight sleep periods). Weeknights and weekends will be measured separately.
    Change in sleep disturbance and impairment
    Measured using the the Patient-Reported Outcomes Measurement Information System (PROMIS) item bank for pediatric sleep. This validated survey generates a sleep disturbance T-score based on items related to sleep onset, sleep continuity and sleep quality in the past week. The survey also generates a sleep-related impairment T-score based on items related to daytime sleepiness, cognition, affect and behavior, and daytime activities in the past week. Higher T-scores indicates poorer sleep quality. Participants will complete this survey at baseline and at the end of each month during the intervention and follow-up periods.
    Change in visceral adipose tissue
    Visceral adipose tissue area will be measured by DXA.
    Change in Body Mass Index (BMI)
    Trained Nutrition Core staff will measure heights and weights of participants. These data will be used to calculate body mass index (kg/m2).
    Change in waist circumference
    Investigators will measure waist circumferences at baseline, 6-months, and 12-months.

    Full Information

    First Posted
    September 12, 2022
    Last Updated
    July 5, 2023
    Sponsor
    Children's Hospital of Philadelphia
    Collaborators
    Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT05703347
    Brief Title
    Optimizing a Mobile Health Platform for Sleep Promotion and Obesity Prevention in Children
    Official Title
    Optimizing a Mobile Health Platform for Sleep Promotion and Obesity Prevention in Children
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    August 2023 (Anticipated)
    Primary Completion Date
    June 2027 (Anticipated)
    Study Completion Date
    June 2027 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Children's Hospital of Philadelphia
    Collaborators
    Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    Yes
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The overall objective of this application is to develop a mobile health platform for the pediatric care setting to promote longer sleep duration for childhood obesity prevention.
    Detailed Description
    Insufficient sleep duration is highly prevalent in childhood and is associated with incident obesity, especially among middle school-aged children. Investigators therefore need to identify strategies to increase sleep duration among children for obesity prevention. The overall objective of this application is to develop a mobile health platform for the pediatric care setting to promote longer sleep duration for childhood obesity prevention. This is a single-site study being conducted at the Children's Hospital of Philadelphia (CHOP). Investigators will randomize 325 children, aged 8-12y, with a body mass index (BMI) between the 50th-95th percentile, and who sleep <8.5 hours per night. Clinical measurements will be acquired at CHOP and sleep will be measured in the home setting. The Way to Health mobile platform will facilitate remote communication and data collection. A validated multi-channel sleep tracker will estimate sleep for 12-months (2-week run-in; 6-month intervention; ≈5.5-month follow-up). A randomized 24 factorial design will assess four components: sleep goal (fixed or modifiable), digital guidance (active or active with virtual study visit), parent incentive (inactive or active), and personalized feedback (inactive or active). The optimal component settings will have to meet the following criteria: increase average baseline sleep duration by ≥30 minutes for ≥75% of intervention weeks and for ≥50% of follow-up weeks. Fat mass will be measured at baseline, 6-, and 12-months using dual energy X-ray absorptiometry (DXA). Total energy intake and the timing and composition of meals will be measured using 24-hour dietary recalls at baseline, 6-, and 12-months. Sociodemographic data will be measured using self-report approaches (e.g., sex, race/ethnicity) and home addresses will be geocoded for geo-spatial analyses.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Insufficient Sleep, Obesity
    Keywords
    insufficient sleep, obesity

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Factorial Assignment
    Model Description
    A computerized random number generated by the Way to Health platform will assign children to 1 of 16 study conditions for a 6-month intervention period. The study conditions differ with respect to: sleep goal (fixed or modifiable), digital sleep guidance (active or active with virtual study visit), parent-directed incentive (inactive or active), and personalized feedback (inactive or active). Our design includes one constant: all participants need to self-monitor their sleep duration by wearing the sleep tracker to allow for daily capture of sleep duration and goal achievement status. The intervention period is therefore designed to test the effectiveness of 4 components, each with two levels, using a factorial design.
    Masking
    Investigator
    Masking Description
    Investigators will be blinded, except the psychologist on the team who needs to train and direct the virtual study visit delivery for one of the intervention components.
    Allocation
    Randomized
    Enrollment
    325 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Condition 1
    Arm Type
    Active Comparator
    Arm Description
    Fixed guideline-based sleep goal, Digital sleep health messaging without virtual study visit consultation, Inactive caregiver-directed loss-framed incentive, Inactive supportive feedback.
    Arm Title
    Condition 2
    Arm Type
    Active Comparator
    Arm Description
    Fixed guideline-based sleep goal, Digital sleep health messaging without virtual study visit consultation, Inactive caregiver-directed loss-framed incentive, Active supportive feedback.
    Arm Title
    Condition 3
    Arm Type
    Active Comparator
    Arm Description
    Fixed guideline-based sleep goal, Digital sleep health messaging without virtual study visit consultation, Active caregiver-directed loss-framed incentive, Inactive supportive feedback.
    Arm Title
    Condition 4
    Arm Type
    Active Comparator
    Arm Description
    Fixed guideline-based sleep goal, Digital sleep health messaging without virtual study visit consultation, Active caregiver-directed loss-framed incentive, Active supportive feedback.
    Arm Title
    Condition 5
    Arm Type
    Active Comparator
    Arm Description
    Fixed guideline-based sleep goal, Digital sleep health messaging with virtual study visit consultation, Inactive caregiver-directed loss-framed incentive, Inactive supportive feedback.
    Arm Title
    Condition 6
    Arm Type
    Active Comparator
    Arm Description
    Fixed guideline-based sleep goal, Digital sleep health messaging with virtual study visit consultation, Inactive caregiver-directed loss-framed incentive, Active supportive feedback.
    Arm Title
    Condition 7
    Arm Type
    Active Comparator
    Arm Description
    Fixed guideline-based sleep goal, Digital sleep health messaging with virtual study visit consultation, Active caregiver-directed loss-framed incentive, Inactive supportive feedback.
    Arm Title
    Condition 8
    Arm Type
    Active Comparator
    Arm Description
    Fixed guideline-based sleep goal, Digital sleep health messaging with virtual study visit consultation, Active caregiver-directed loss-framed incentive, Active supportive feedback.
    Arm Title
    Condition 9
    Arm Type
    Active Comparator
    Arm Description
    Personalized sleep goal, Digital sleep health messaging without virtual study visit consultation, Inactive caregiver-directed loss-framed incentive, Inactive supportive feedback.
    Arm Title
    Condition 10
    Arm Type
    Active Comparator
    Arm Description
    Personalized sleep goal, Digital sleep health messaging without virtual study visit consultation, Inactive caregiver-directed loss-framed incentive, Active supportive feedback.
    Arm Title
    Condition 11
    Arm Type
    Active Comparator
    Arm Description
    Personalized sleep goal, Digital sleep health messaging without virtual study visit consultation, Active caregiver-directed loss-framed incentive, Inactive supportive feedback.
    Arm Title
    Condition 12
    Arm Type
    Active Comparator
    Arm Description
    Personalized sleep goal, Digital sleep health messaging without virtual study visit consultation, Active caregiver-directed loss-framed incentive, Active supportive feedback.
    Arm Title
    Condition 13
    Arm Type
    Active Comparator
    Arm Description
    Personalized sleep goal, Digital sleep health messaging with virtual study visit consultation, Inactive caregiver-directed loss-framed incentive, Inactive supportive feedback.
    Arm Title
    Condition 14
    Arm Type
    Active Comparator
    Arm Description
    Personalized sleep goal, Digital sleep health messaging with virtual study visit consultation, Inactive caregiver-directed loss-framed incentive, Active supportive feedback.
    Arm Title
    Condition 15
    Arm Type
    Active Comparator
    Arm Description
    Personalized sleep goal, Digital sleep health messaging with virtual study visit consultation, Active caregiver-directed loss-framed incentive, Inactive supportive feedback.
    Arm Title
    Condition 16
    Arm Type
    Experimental
    Arm Description
    Core intervention, Sleep goal, Sleep guidance messaging, Caregiver-directed loss-framed incentive, Supportive feedback.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Fixed sleep goal
    Intervention Description
    Investigators will determine if a fixed guideline-based goal (≥9 hours per night) is more efficacious for increasing sleep duration.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Personalized sleep goal
    Intervention Description
    Investigators will determine if a personalized goal (≥9 hours per night, but can be lowered to a personalized level, capped at +30 minutes per night above baseline) is more efficacious for increasing sleep duration.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Digital sleep health messaging without virtual study visit
    Intervention Description
    All participants will receive digital sleep health messaging. Messaging will focus on evidence-based sleep health recommendations, such as regulating evening electronics use, managing extracurricular activities, and setting consistent bedtime routines and sleep-wake schedules. This group will NOT have virtual psychological visits.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Digital sleep health messaging with virtual study visit
    Intervention Description
    All participants will receive digital sleep health messaging. Messaging will focus on evidence-based sleep health recommendations, such as regulating evening electronics use, managing extracurricular activities, and setting consistent bedtime routines and sleep-wake schedules. The participants will be randomized to additionally receive virtual study visits where doctoral-level psychology trainees will be trained to implement evidence-based behavioral sleep health guidance.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Inactive Parent-Directed Loss-Framed Incentive
    Intervention Description
    No parental incentive
    Intervention Type
    Behavioral
    Intervention Name(s)
    Active Parent-Directed Loss-Framed Incentive
    Intervention Description
    Parents will receive a financial incentive when their child achieves their sleep goal. The incentive will be loss-framed; parents will receive an endowment of $10 at the start of each intervention week, in a virtual bank account; Investigators will deduct $2 each weeknight the sleep duration goal is not met; the funds remaining in the virtual account will be dispensed each Sunday. The weekly endowment-payment approach allows for fresh starts each week. The incentive will be directed at parents as a method to enhance engagement. Investigators will ask parents at baseline and at the end of each month to rate their perceived support in helping their child to meet their sleep duration goal.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Inactive Supportive Feedback
    Intervention Description
    No supportive feedback
    Intervention Type
    Behavioral
    Intervention Name(s)
    Active Supportive Feedback
    Intervention Description
    Participants will receive a weekly performance summary message each Sunday during the intervention period, with supportive feedback included to motivate children to maintain their good performance in the week ahead, or to try and improve upon a weak or moderate performance in the week ahead. Investigators will ask children will complete an online survey each Sunday to measure how motivated they are to achieve their sleep goal in the week ahead.
    Primary Outcome Measure Information:
    Title
    Change in sleep duration
    Description
    The primary outcome for aims 1 and 3 is change in nighttime sleep duration (hours per night) on weeknights measured by a sleep tracker with high sensitivity and moderate specificity for measuring sleep.
    Time Frame
    baseline to 12 months
    Title
    Change in fat mass index Z-score
    Description
    Aim 2 primary outcome. Total body fat mass will be measured by DXA. Fat mass index (FMI, kg of fat divided by height in meters squared) will be calculated, and age and gender specific FMI Z-scores will be determined using U.S. specific FMI growth charts.
    Time Frame
    Baseline to 12 months
    Secondary Outcome Measure Information:
    Title
    Change in sleep onset
    Description
    Change in sleep onset (time subject falls asleep). Weeknights and weekends will be measured separately.
    Time Frame
    Baseline to 12 months
    Title
    Change in sleep offset
    Description
    Change in sleep offset (time subject wakes up). Weeknights and weekends will be measured separately.
    Time Frame
    Baseline to 12 months
    Title
    Change in sleep midpoint
    Description
    Change in sleep midpoint. Weeknights and weekends will be measured separately.
    Time Frame
    Baseline to 12 months
    Title
    Change in social jetlag
    Description
    Investigators will calculate "social jetlag" by subtracting the weekend night sleep midpoint from the weeknight sleep midpoint. Social jetlag provides an indication of the discrepancy between internal biological clocks and social requirements and has been linked to cardiometabolic risk.
    Time Frame
    up to 12 months
    Title
    Change in sleep efficiency
    Description
    Change in sleep efficiency (percentage of time spent asleep during overnight sleep periods). Weeknights and weekends will be measured separately.
    Time Frame
    Baseline to 12 months
    Title
    Change in sleep onset latency
    Description
    Change in sleep onset latency (time to fall asleep). Weeknights and weekends will be measured separately.
    Time Frame
    Baseline to 12 months
    Title
    Change in wake after sleep onset
    Description
    Change in wake after sleep onset (time awake during overnight sleep periods). Weeknights and weekends will be measured separately.
    Time Frame
    Baseline to 12 months
    Title
    Change in sleep disturbance and impairment
    Description
    Measured using the the Patient-Reported Outcomes Measurement Information System (PROMIS) item bank for pediatric sleep. This validated survey generates a sleep disturbance T-score based on items related to sleep onset, sleep continuity and sleep quality in the past week. The survey also generates a sleep-related impairment T-score based on items related to daytime sleepiness, cognition, affect and behavior, and daytime activities in the past week. Higher T-scores indicates poorer sleep quality. Participants will complete this survey at baseline and at the end of each month during the intervention and follow-up periods.
    Time Frame
    Baseline to 12 months
    Title
    Change in visceral adipose tissue
    Description
    Visceral adipose tissue area will be measured by DXA.
    Time Frame
    Baseline to 12 months
    Title
    Change in Body Mass Index (BMI)
    Description
    Trained Nutrition Core staff will measure heights and weights of participants. These data will be used to calculate body mass index (kg/m2).
    Time Frame
    Baseline to 12 months
    Title
    Change in waist circumference
    Description
    Investigators will measure waist circumferences at baseline, 6-months, and 12-months.
    Time Frame
    Baseline to 12 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    8 Years
    Maximum Age & Unit of Time
    12 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Aged 8-12 years olds. Insufficient sleep duration (<8.5 hours per night). Body mass index (BMI) between the 50th and 95th percentile for age and sex. One child per family. Exclusion Criteria: Diagnosed with a chronic disease. Diagnosed with a behavioral health problem. Diagnosed with a condition that can impact sleep or growth. Diagnosed with a condition affecting physical growth and maturation or dietary intake. Children with a history of cancer, kidney, GI, musculoskeletal, or sleep disorders. Children who will transition to high-school during the study. Children using steroids/hormones. Children regularly taking medications
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Jonathan Mitchell, PhD
    Phone
    2674261473
    Email
    mitchellj2@chop.edu
    First Name & Middle Initial & Last Name or Official Title & Degree
    Christa Seidman, MSPH
    Phone
    2157153442
    Email
    seidmancl@chop.edu
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Jonathan Mitchell, PhD
    Organizational Affiliation
    Children's Hospital of Philadelphia
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
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    Optimizing a Mobile Health Platform for Sleep Promotion and Obesity Prevention in Children

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