Parent Supported Weight Reduction in Down Syndrome
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About
The purpose of this study is to determine whether a nutrition and physical activity education program for families of overweight or obese adolescents with Down syndrome is more effective when behavioral lifestyle change strategies are added.
Full description
Children with intellectual disabilities, including Down syndrome (DS), are as likely to be overweight than their typically developing peers. The consequences of childhood obesity include increased risk for Type-2 diabetes, orthopedic problems, sleep apnea, elevated cardiovascular risk and menstrual irregularities. Research indicating a high prevalence of overweight, obesity, low fitness levels and other health problems among adults with DS suggest the need for more attention to health promotion among adolescents with DS, which has been limited to date. Educational interventions in nutrition and physical activity have not been tested through randomized clinical trial with families of adolescents with DS; nor have behavioral "lifestyle change" interventions based on Social Cognitive Theory. Among typical populations, the addition of training in behavior and lifestyle change to education-alone interventions increasingly is being seen as critical in helping to promote long-term weight loss and weight maintenance. The hypothesis of this study is that a parent supported weight reduction (PSWR) intervention that combines behavioral strategies with nutrition and activity education (NAE) will be more effective in reducing overweight in adolescents with DS than a program that provides NAE alone or a Wait-List (WL) control.
Enrollment
Sex
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Volunteers
Inclusion criteria
- Age 13-26 with Down syndrome
- Living at home in single- or two-parent family, w/no plans to leave home in next year
- Achieves IQ score 45 or above on the Kaufman Brief Intelligence Test (K-BIT)
- Academic ability and necessary behavioral/social control to participate in a group classroom-based educational program
- Clinically overweight, as indicated by a BMI at or above 85th percentile for age and gender
- Signed approval to participate, which includes a completed recent thyroid screen, provided by participant's Primary Physician (and participant's cardiologist is he/she has a history of a heart condition), and participant's neurologist if he/she has a history of seizures)
Exclusion criteria
- Untreated thyroid disorder
- Type I or II Diabetes
- Cardiac problem, treated or untreated, for whom the participant's treating cardiologist indicates restrictions in physical activity
- Epilepsy/seizure disorder in which participant is not stable on medications
- Orthopedic injuries or deformities
- Chronic GI illness (except constipation) including inflammatory bowel diseases and celiac disease
- Prader Willi syndrome
- Unwillingness to wear accelerometer at screening or enrollment
- Non-ambulatory, i.e., uses wheelchair or other assistive devices for moving about and walking
- Chronic/severe foot infection (as screened by physical therapist, but in coordination with physician)
- Severe balance problems (as screened by physical therapist)
- Resting heart rate less than 50 beats per minute (bpm), or greater to or equal to 100 bpm (observed in physical therapy screening)
- History of major medical illness (i.e., cancer, leukemia)
- History of profound behavioral problems, i.e., self injury, injury to others, property destruction, etc.
- Other diagnosed disorders, including autism spectrum disorders, bipolar disorder (within the last year), eating disorder (within the last year), major depression (within the last year), psychosis & schizophrenia
- Other exclusion conditions left to the discretion of the study team
Trial design
Primary purpose
Allocation
Interventional model
Masking
21 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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