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Enhancing Sleep Duration: Effects on Children's Eating and Activity Behaviors-Renewal

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Temple University

Status

Completed

Conditions

Obesity
Sleep

Treatments

Behavioral: Optimize Sleep (OS)
Behavioral: Optimize Sleep-Plus (OS-Plus)

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT03186508
R01HL092910

Details and patient eligibility

About

Enhancing children's sleep may be a novel approach for prevention of obesity and cardiovascular (CV) disturbance. Observational studies with children demonstrate that short sleep increases risk of obesity and other CV risk factors. Randomized controlled trials with children 8-11 years old demonstrate that enhancing sleep duration leads to positive changes in eating and activity behaviors and weight status, particularly for children who enhance their sleep the most. Enhancing sleep may be particularly important for racial minority children and those from lower socioeconomic backgrounds given their increased risk for short sleep, obesity and CV risk factors. In this study two active obesity preventive interventions will be evaluated: a) enhancing sleep alone (Optimize Sleep [OS]), and b) enhancing sleep along with eating and activity behaviors that have demonstrated efficacy for obesity prevention and are implicated in self-regulatory pathways related to sleep (i.e., energy dense snack foods and beverages, TV viewing, and physical activity) (OS-Plus). Two hundred four children 6-11 years old who are primarily African American/black, primarily from low socioeconomic backgrounds, and who sleep < 9.5 hours/night into a 12-month study will be enrolled. Children will be randomly assigned to either OS or OS-Plus. Over the 6-month treatment phase, all children will attend an 8-session treatment; monthly phone contacts will occur during maintenance (6-12 months). Primary aim is to determine the efficacy of OS-Plus relative to OS on change in body mass index z-score (BMIz) at end of treatment. Secondary aims will assess efficacy of OS-Plus relative to OS on additional cardiometabolic risk factors, eating and activity behaviors. Exploratory aims will assess maintenance of effects at 12 months.

Enrollment

149 patients

Sex

All

Ages

6 to 11 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Caregiver-reported child age of 6-11 years
  2. < 9.5 Hours time-in-bed for sleep most days/week
  3. BMI for age and gender > 25th percentile (but no greater than 100% overweight)
  4. Understanding of and ability to complete protocol
  5. Self-reported caregiver age of 18 years and primary caregiver at bedtimes/wake times
  6. Likes food used in the eating regulation paradigms
  7. Willingness to be randomized to either treatment condition.

Exclusion criteria

  1. Diagnosable sleep disorder
  2. Medication use or diagnosis of medical or psychiatric condition that may impact sleep/weight status
  3. Current or planned treatment for weight control
  4. Allergies or dietary restrictions that would prevent consumption of foods used in the study

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

149 participants in 2 patient groups

Optimize Sleep (OS)
Active Comparator group
Description:
Optimize Sleep will focus exclusively on enhancing sleep by using effective behavioral strategies. Specific strategies to be used include: goal setting and self-monitoring, positive bedtime routines, stimulus control/sleep hygiene strategies, problem-solving regarding challenges, and review of effective strategies for relapse prevention.
Treatment:
Behavioral: Optimize Sleep (OS)
Optimize Sleep-Plus (OS-Plus)
Active Comparator group
Description:
OS-Plus will focus on enhancing sleep and targeted eating (decreasing sugar-sweetened beverages and sweet and salty snack foods) and activity (increasing physical activity and decreasing TV viewing) behaviors. Specific strategies to be used include: goal setting and self-monitoring, positive bedtime routines, stimulus control/sleep hygiene strategies, problem-solving regarding challenges, and review of effective strategies for relapse prevention.
Treatment:
Behavioral: Optimize Sleep-Plus (OS-Plus)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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