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NCT Number: NCT05703347

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

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.

Recruiting

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Key information

Age range

8 year–12 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, 19104, United States

Location status: Recruiting

Location contact

Jonathan Mitchell, PhD

CONTACT

[email protected]

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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 related to exclusionary medical conditions or that impact sleep.
  • Children with a history of significant behavioral health concerns.
  • Parent reported PROMIS Parent Proxy Sleep Disturbance - Short Form 8a raw score of ≥28.

Treatment and study plan

Fixed sleep goal

Behavioral

Investigators will determine if a fixed guideline-based goal (≥9 hours per night) is more efficacious for increasing sleep duration.

Personalized sleep goal

Behavioral

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.

Digital sleep health messaging without virtual study visit

Behavioral

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.

Digital sleep health messaging with virtual study visit

Behavioral

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.

Inactive Parent-Directed Loss-Framed Incentive

Behavioral

No parental incentive

Active Parent-Directed Loss-Framed Incentive

Behavioral

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.

Inactive Supportive Feedback

Behavioral

No supportive feedback

Active Supportive Feedback

Behavioral

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 outcomes

  1. Change in sleep duration

    Time frame: baseline to 12 months

    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.

  2. Change in fat mass index Z-score

    Time frame: Baseline to 12 months

    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 outcomes

  1. Change in sleep onset

    Time frame: Baseline to 12 months

    Change in sleep onset (time subject falls asleep). Weeknights and weekends will be measured separately.

  2. Change in sleep offset

    Time frame: Baseline to 12 months

    Change in sleep offset (time subject wakes up). Weeknights and weekends will be measured separately.

  3. Change in sleep midpoint

    Time frame: Baseline to 12 months

    Change in sleep midpoint. Weeknights and weekends will be measured separately.

  4. Change in social jetlag

    Time frame: up to 12 months

    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.

  5. Change in sleep efficiency

    Time frame: Baseline to 12 months

    Change in sleep efficiency (percentage of time spent asleep during overnight sleep periods). Weeknights and weekends will be measured separately.

  6. Change in sleep onset latency

    Time frame: Baseline to 12 months

    Change in sleep onset latency (time to fall asleep). Weeknights and weekends will be measured separately.

  7. Change in wake after sleep onset

    Time frame: Baseline to 12 months

    Change in wake after sleep onset (time awake during overnight sleep periods). Weeknights and weekends will be measured separately.

  8. Change in sleep disturbance and impairment

    Time frame: Baseline to 12 months

    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.

  9. Change in visceral adipose tissue

    Time frame: Baseline to 12 months

    Visceral adipose tissue area will be measured by DXA.

  10. Change in Body Mass Index (BMI)

    Time frame: Baseline to 12 months

    Trained Nutrition Core staff will measure heights and weights of participants. These data will be used to calculate body mass index (kg/m2).

  11. Change in waist circumference

    Time frame: Baseline to 12 months

    Investigators will measure waist circumferences at baseline, 6-months, and 12-months.

Study contacts

Contact information is provided by the study sponsor or research team.

Abby Salem

CONTACT

[email protected]

2155902386

Jonathan Mitchell, PhD

CONTACT

[email protected]

2674261473

Sponsors and collaborators

Lead sponsor

Children's Hospital of Philadelphia

Other

Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
  • University of Pennsylvania

Registry information

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
Jan 30, 2023
Registry last updated
May 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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