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Acceptance-based Care for Child Eating and Physical Activity Treatment

Addressing Healthcare Disparities in Pediatric Obesity Treatment: Development of a Novel, Patient-centered Intervention Targeting Executive Function

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03368716
Acronym
ACCEPT
Enrollment
184
Registered
2017-12-11
Start date
2019-02-04
Completion date
2022-01-31
Last updated
2022-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Executive Function, Pediatric Obesity, Self-Regulation

Keywords

Pediatric Obesity, Executive Function, Behavioral Intervention, Self-Regulation, Acceptance-Based

Brief summary

The purpose of this study is to develop and pilot test a new type of patient-centered, family-based treatment for children aged 8-12 with obesity and their caregivers. The treatment will focus specifically on improving children's self-regulation (SR) skills to help them better manage their feelings, behaviors, and thoughts to help them live a healthier lifestyle.

Detailed description

We aim to: (1) To determine the treatment needs of children ages 8-12 with obesity and their families with a focus on understanding cognitive function challenges that are related to self-regulation (using focus groups i.e. FG and feedback sessions i.e. FB). (2) To evaluate the feasibility and acceptability of this novel family-based treatment. (3) Explore potential associations between pediatric cardiovascular (CVD) risk factors and self-regulation in children with and without overweight or obesity. (4) To refine the F-ABT protocol and to maximize participant feasibility, acceptability, safety, and tolerability of F-ABT. (5) To provide pilot, proof-of-concept, and preliminary efficacy data of beneficial effects of F-ABT on SR and BMI in children with SR deficits and their caregivers.

Interventions

BEHAVIORALAcceptance-based Behavioral Treatment (ABBT)

ABBT is rooted in behavioral therapy but also cultivates self-regulation skills including experiential acceptance of potentially uncomfortable internal experiences (e.g., emotions, cravings), mindful awareness of decision making (e.g., mindful eating), and values clarification and behavioral commitment (e.g., practicing daily physical activity to be a contributing member on a sports team). ABBT has been used effectively to help youth and adults manage various medical and psychological problems. Moreover, components of ABBT have been shown to improve child and adult EF including inhibitory control and cognitive flexibility. Recently, ABBT has been integrated with components of standard behavioral treatment of obesity and applied with robust efficacy to weight management in adults.

Sponsors

Kaul Pediatric Research Institute of the Alabama Children's Hospital Foundation
CollaboratorUNKNOWN
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
University of Alabama at Birmingham
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
8 Years to 12 Years
Healthy volunteers
Yes

Inclusion criteria

\- Children who: (1) have a BMI ≥ 85th percentile; (2) are ≥8 and ≤12 years old at the beginning of treatment; (3) can read, write, and speak English, along with their caregiver; (4) plan to stay living in the local area during the study period; (5) have a consenting caregiver who can commit to all study procedures and provide reliable travel.

Exclusion criteria

\- Children who:(1) comorbid developmental/intellectual disability/traumatic brain injury/other identified condition known to substantially impact EF and/or weight management; (2) taking medication that is known to affect weight or appetite, (3) recent infection that may cause confounds of acute inflammation, (4) have an uncorrected visual or hearing impairment that would prohibit completion of cognitive testing, and (5) are unable to use an iPad with appropriate training for cognitive testing. The children without obesity (n=32) will have normal-range BMI scores (5th ≤BMI percentile\< 85th) but otherwise follow the same inclusion/

Design outcomes

Primary

MeasureTime frameDescription
High-sensitivity reactive protein (hsCRP)Baseline to 4.5 monthsmg/L
Change in child body mass indexBaseline to 4.5 monthsChild height and weight measurements will be converted to zBMI using CDC age and sex specific scales.
Change in child objective executive functionBaseline to 4.5 monthsPerformance-based EF will be tested using the NIH Toolbox Cognitive Battery which measures executive function (inhibitory control and cognitive flexibility), attention, episodic memory, language, processing speed, and working memory. T-scores will be used for each domain. Higher t-scores indicate better function.
Change in child subjective executive functionBaseline to 4.5 monthsSubjective EF will be measured using the Behavioral Rating Inventory of Executive Function. The Global Severity Index will be used which is interpreted using T-scores. Higher t-scores indicate better function.
Change in Health-Related Quality of LifeBaseline to 4.5 monthsSizing Me Up© & Sizing Them Up© are validated obesity-specific self-report and parent-report measures, respectively, of health-related quality of life for children 5-13 years old that measure functioning in a variety of areas (e.g., emotional, physical, teasing/marginalization). The Total Score will be used as the outcome, which is a scaled score ranging from 0-100 with higher scores representing better quality of life.
CortisolBaseline to 4.5 monthsug/dl
Blood pressureBaseline to 4.5 monthsSystolic over diastolic
Fasting glucoseBaseline to 4.5 monthsmg/dl
Low-density lipoprotein (LDL-C) cholesterolBaseline to 4.5 monthsmg/dl
High-density lipoprotein (HDL-C) cholesterolBaseline to 4.5 monthsmg/dl
TriglycerideBaseline to 4.5 monthsmg/dl
InsulinBaseline to 4.5 monthsuU/ml
Hemoglobin A1CBaseline to 4.5 monthsPercentage
LeptinBaseline to 4.5 monthsng/mL
Tumor necrosis factor (TNF-a)Baseline to 4.5 monthspg/ml
Interleukin (IL-6)Baseline to 4.5 monthspg/ml

Secondary

MeasureTime frameDescription
Child eating behaviorBaseline to 4.5 monthsThe Children's Eating Behaviour Questionnaire is a 35-item parent proxy-report measure of eating behavior producing 8 subscales: responsiveness to food, enjoyment of food, satiety responsiveness, slowness in eating, fussiness, emotional overeating, emotional undereating, desire for drinks. Items are scored on a 5-point Likert scale and the mean score of each subscale is used. Higher scores indicate more eating behaviors in a certain domain.
Dietary behaviorBaseline to 4.5 monthsChild and parent dietary habits will be assessed via self-report throughout the intervention using the online USDA SuperTracker software.
Physical activity behaviorBaseline to 4.5 monthsChild and parent physical activity habits will be assessed via self-report throughout the intervention using the online USDA SuperTracker software.
MindfulnessBaseline to 4.5 monthsThe Child Acceptance and Mindfulness Measure (CAMM) is a 10-item measure of children's awareness and acceptance of their own private events or internal experiences. Items are reverse scored on a 5-point Likert scale. Higher scores correspond to higher levels of mindfulness.
Psychological flexibilityBaseline to 4.5 monthsThe Avoidance and Fusion Questionnaire for Youth (AFQ-Y) is a 17-item self-report measure for to assess psychological inflexibility in children. Items are scored on a 5-point Likert scale and summed for a total score ranging between 0-68. Higher scores are indicative of greater psychological inflexibility. The Parental Acceptance and Action Questionnaire (PAAQ) is a 15-item measure that evaluates parents' experiential acceptance and action tendencies in the context of their relationship with their children. The Total score is used which is a sum of all items which are rated on a 7-point Likert scale. Higher scores represent a greater degree of parental experiential avoidance.
Impact of the food environmentBaseline to 4.5 monthsThe Children's Power of Food Scale is a 15-item self-report assessment of the psychological impact of living in food-abundant environments. Items are rated on a 5-point Likert scale and summed to create a total score. Higher scores reflect greater responsiveness to the food environment.
Child body fat percentBaseline to 4.5 monthsThe Tanita SC-240 BIA device has been validated for use with children to assess total body fat to the nearest 0.1%. Total body fat percent will be standardized using age and sex specific CDC conversions.
Waist circumferenceBaseline to 4.5 monthsThe Gulick II anthropometric tape will be utilized to measure children's waist circumference, which will be converted to national published standardized (z) scores.

Other

MeasureTime frameDescription
DemographicsBaselineChild and caregiver characteristics such as age, sex, race/ethnicity, educational level, family income, and marital status will be assessed via caregiver report at baseline only.
Participant satisfaction - surveys9 weeks, 18 weeksSurveys will assess the utility of intervention content, intervention burden and satisfaction, participation barriers, and suggestions for change.
Program feasibility - interviews9 weeks, 18 weeksSemi-structured group interviews will assess caregiver and child experiences with the program.
Program feasibility - surveys9 weeks, 18 weeksSurveys will assess the utility of intervention content, intervention burden and satisfaction, participation barriers, and suggestions for change.
Adherence - attendance9 weeks, 18 weeksThe number of sessions attended will be the primary indicator of adherence.
Adherence - self-monitoring9 weeks, 18 weeksAs a secondary measure, we will use the number of days that self-monitoring records were completed. A completed self-monitoring record should have at least 2 meals and the total number of exercise minutes recorded per day.
Participant satisfaction - interviews9 weeks, 18 weeksSemi-structured group interviews will assess caregiver and child experiences with the program.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026