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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02677792
Other study ID # #2015-0155
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 2016
Est. completion date December 2022

Study information

Verified date February 2023
Source University of Mississippi Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the current study is examine the feasibility and efficacy of providing a behavioral family intervention in 30 youth 10 to 17 years of age who are obese and attending a multidisciplinary pediatric obesity clinic and their parents. Participating families will complete assessments consisting of weight status, dietary intake, physical activity, health-related quality of life, psychological functioning, home-food environment, parenting skills, and self-efficacy at pre-treatment (Baseline), post-treatment (Month 3), and 2 month post-treatment follow-up (Month 5). Family attendance data will be collected during the behavioral family intervention and children and parents will complete a treatment satisfaction questionnaire at the post-treatment assessment. Health outcomes (e.g., A1C, glucose) routinely assessed through standard medical care in the multidisciplinary pediatric obesity clinic will be obtained from child medical charts.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date December 2022
Est. primary completion date December 2020
Accepts healthy volunteers No
Gender All
Age group 10 Years to 17 Years
Eligibility Inclusion Criteria: 1. child 10 to 17 years of age attending an outpatient pediatric obesity clinic visit 2. child or adolescent is obese (equal to or above the 95th percentile for BMI based on Centers for Disease Control and Prevention (CDC) norms for age and gender) 3. child or adolescent is accompanied by a parent or legal guardian 4. participating child and parent speak and read English 5. family agrees to attend group meetings at a medical clinic over a 3 month period Exclusion Criteria: 1. participating child or parent, according to parent report, has dietary restriction or medical condition contraindicating mild energy restriction or moderate physical activity (e.g., musculoskeletal, heart, or respiratory condition, uncontrolled blood pressure or exercise induced asthma) 2. child diagnosed according to parent report with pervasive developmental delay (e.g., autistic disorder) 3. child or parent, according to parent report, in commercial weight loss program 4. child or parent currently prescribed medications to impact appetite or weight loss/gain, according to parent report 5. parent and child do not speak and read English

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Behavioral Family Intervention (BFI)
Participating families will receive standard medical care through the Wellness and Weight Clinic, as well as the BFI. The BFI is based on family systems (Minuchin et al., 1975) and social-cognitive (Bandura, 1998) theories. Each dyad will participate in simultaneous, but separate, 75-minute parent and child groups over a 3 month period. The groups will start off meeting every week for 8 weeks and then bi-weekly for 1 month. Thus, dyads will attend a total of 10 group meetings over the 3 month period (12.5 hours of total treatment contact).

Locations

Country Name City State
United States University of Mississippi Medical Center Jackson Mississippi

Sponsors (1)

Lead Sponsor Collaborator
University of Mississippi Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Change in Child Self-Efficacy for Total Healthy Lifestyle Behaviors Child-report questionnaire; sum of scores from Child Dietary Self-Efficacy Scale and Self-Efficacy for Physical Activity Scale Baseline, Post-Treatment (Month 3), and Follow-up (Month 5)
Other Change in Child-Reported Total Health-Related Quality of Life Child-report; total score from Pediatric Quality of Life Inventory Baseline, Post-Treatment (Month 3), and Follow-up (Month 5)
Other Change in Parent-Reported Total Health-Related Quality of Life Parent-report; total score from Pediatric Quality of Life Inventory Baseline, Post-Treatment (Month 3), and Follow-up (Month 5)
Other Change in Child Psychological Functioning (Total Problems Subscale from CBCL) parent-report; Child Behavior Checklist (CBCL) Total Problems Scale Baseline, Post-Treatment (Month 3), and Follow-up (Month 5)
Other Change in Home Food Inventory Obesiogenic Food Availability Score Parent-reported Baseline, Post-Treatment (Month 3), and Follow-up (Month 5)
Other Change in Total Parenting Competence Parent-report; Total score from Parenting Sense of Competency (PSOC) Scale Baseline, Post-Treatment (Month 3), and Follow-up (Month 5)
Primary Change in Child Weight Status (BMIz) BMIz calculated from measured child height and weight Baseline, Post-Treatment (Month 3), and Follow-up (Month 5)
Secondary Change in Total Child Physical Activity kcals from Block Kids Physical Activity Screener Child-report questionnaire Baseline, Post-Treatment (Month 3), and Follow-up (Month 5)
Secondary Change in Child Dietary Intake Total kcals from 24-hour dietary recall Child-report 24-hour dietary recall assessed via Automated Self-administered 24-hour recall (ASA24) System; Children will complete the ASA-2014-Kids Baseline, Post-Treatment (Month 3), and Follow-up (Month 5)
Secondary Change in Child A1C Values From child medical chart - testing completed as part of standard medical care Baseline, Post-Treatment (Month 3), and Follow-up (Month 5)
Secondary Change in Child Glucose Values From child medical chart - testing completed as part of standard medical care Baseline, Post-Treatment (Month 3), and Follow-up (Month 5)
Secondary Change in Parent Weight Measured parent weight Baseline, Post-Treatment (Month 3), and Follow-up (Month 5)
Secondary Change in Total Parent Physical Activity kcals from Block Physical Activity Screener Adults Parent-report questionnaire Baseline, Post-Treatment (Month 3), and Follow-up (Month 5)
Secondary Change in Parent Dietary Intake Total kcals from 24-hour dietary recall Parent-report 24-hour dietary recall assessed via ASA24-2014 Baseline, Post-Treatment (Month 3), and Follow-up (Month 5)
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