Ideas Moving Parents and Adolescents to Change Together (IMPACT) (IMPACT)
Overweight, Obese

About this trial
This is an interventional treatment trial for Overweight focused on measuring Overweight, Obese, Over Nutrition, Nutrition Disorders, Body weight, Signs and Symptoms
Eligibility Criteria
Inclusion Criteria:
- Students entering the 6th grade who are found at the standard school screenings to be overweight or obese
- (BMI 85th- 94th percentile or > 95th percentile for age/sex respectively)
Exclusion Criteria:
- Taking medications that alter appetite or weight (e.g. glucocorticoids, metformin, insulin, Risperidone (Risperdal), Olanzapine (Zyprexa), Clozapine(Clozaril), Quetiapine (Seroquel), Ziprasidone (Geodon), Carbamazepine (Tegretol), Valproic acid (Depakote/Depakene/Depacon), Aripiprazole (Abilify), Orlistat (Xenical), Sibutramine (Meridia), Phentermine, Diethylproprion (Tenuate), Topirimate (Topamax), glitazones (thiazolidinediones)
- Inability to understand English
- Stage 2 hypertension or stage 1 hypertension with end organ damage (left ventricular hypertrophy, microalbuminuria)
- Severe behavioral problems that preclude group participation (as reported by parent/guardian)
- Child involvement in another weight management program
- Family expectation to move from the region within 1 year
- The presence of a known medical condition that itself causes obesity (e.g., Prader-Willi syndrome) or interfere with HbA1C ( sickle cell disease)
Sites / Locations
- Case Western Reserve University
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
No Intervention
HealthyCHANGE
SystemCHANGE
Tools4CHANGE
Cognitive behavioral strategies to address diet, physical activity, sedentary behavior and sleep for children.
Intervention (based on systems improvement and choice architecture theories) System improvement and choice architecture theories seek to teach a set of skills using family self-designed experiments to redesign daily routines
In contrast to the behavioral arms, youths with their parent(s)/guardian randomized to this group will have one 60-minute face-to-face meeting at initiation of the study with a dietitian who is also trained in recommendations for exercise and sedentary behavior.