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Efficacy of a Clinic-based, Multi- Disciplinary, Pediatric Weight Management Program

Efficacy of a Clinic-based, Multi- Disciplinary, Pediatric Weight Management Program

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01857791
Acronym
REWARD Teens
Enrollment
40
Registered
2013-05-20
Start date
2011-01-31
Completion date
Unknown
Last updated
2015-09-10

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

Conditions

Body Weight Changes

Brief summary

Childhood obesity has more than tripled in the past 30 years. From 1980 to 2008, the prevalence of obesity among adolescents aged 12 to 18 years, increased from 5.0% to 18.1%.1 Although several pediatric weight management programs are available, access to these programs may not always be possible. The proposed study will be an ongoing research program with approximately 40 children ages 12-18 years enrolled into the study over a year. All study participants will participate in a baseline evaluation which will include body composition measures, aerobic testing, as well as nutrition and physical activity questionnaires. Study participants will be assigned to the clinic-based group. The clinic- based group will participate in a 12-week multi-disciplinary weight management program. All study participants will then participate in a 12-week follow-up evaluation similar to the baseline visit. New participants will be enrolled every 12 weeks. Every 12 weeks, active participants (those that have completed a minimum of 12 weeks) will have the option to continue in the program or, discontinue their active participation in the program and enroll into the maintenance phase which will consist of measures only every 12 weeks. The objective of the proposed study includes examining the efficacy of the clinic-based, multi-disciplinary, pediatric weight management program.

Interventions

BEHAVIORALmultidisciplinary, behavior modification

Sponsors

University of Vermont
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Phone screening * Approval to participate in a weight management program from the child's pediatrician * Children between the ages of 12 and 18 years * Children overweight (\>85th-\<95th BMI percentile) or obese (\>95th BMI percentile)

Exclusion criteria

* Children with evidence of significant cardiovascular disease or cardiac arrhythmias * Children with liver disease * Children on chronic use of medications including diuretics, steroids and adrenergic-stimulating agents * Children with emotional problems such as clinical depression or other diagnosed psychological condition and currently use prescription medication for psychological conditions * Children with evidence of family and/or medical neglect or physical, mental or sexual child abuse

Design outcomes

Primary

MeasureTime frameDescription
weight loss12 weeksBody weight will be measured at baseline and at 12-weeks. Mean percentage weight change will be assessed following the 12-week intervention.

Countries

United States

Contacts

Primary ContactConnie Tompkins, PhD
Connie.Tompkins@uvm.edu8026563817

Outcome results

None listed

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