Primary Care Treatment for Overweight Adolescent Females (SHINE)
NCT ID: NCT01068236
Last Updated: 2010-03-24
Study Results
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Basic Information
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COMPLETED
PHASE2
215 participants
INTERVENTIONAL
2005-08-31
2009-12-31
Brief Summary
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Detailed Description
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We propose to examine the clinical effectiveness and incremental cost-effectiveness of a primary care-based multi-component lifestyle intervention for overweight adolescent females and their families. This multi-component intervention will be tailored for gender and developmental stage, and will include a behaviorally-based intervention for teens and parents as well as coordinated feedback and counseling from the adolescent's pediatric primary care provider (PCP). We will compare the primary care-based intervention to a usual-care control condition in which adolescents and their family receive information about weight loss and guidelines for achieving and maintaining a healthy lifestyle along with the encouragement to utilize any appropriate health care services.
The principal aim of the study is to determine the clinical effectiveness of a primary care-based, multi-component lifestyle intervention for overweight (≥ 90th percentile) adolescent females and their families. H1: We hypothesize that the treatment group will have a greater decrease in BMI z-score from baseline to 12 months than the control youth.
In addition, we include the following secondary aims that are exploratory and intended to be hypothesis-generating rather than hypothesis-testing activities:
Determine if dietary intake (total energy intake, % calories from fat, etc.) and/or physical activity mediate the effect of the intervention on BMI z score. H2: Change in dietary intake and physical activity from baseline to 6 months will mediate the relationship between the intervention and change in BMI z score from baseline to 12 months.
Determine the impact of the experimental intervention for overweight adolescents and their families on the secondary outcomes including other physiological parameters (triglycerides, cholesterol, fasting insulin), quality of life, and psychosocial functioning; participant safety (depression and disordered eating behaviors); and feasibility/acceptability of the intervention (e.g., participant and provider satisfaction) in preparation for future Phase III trials.
Determine the incremental cost-effectiveness of the intervention relative to usual care from the societal perspective. We will examine the direct cost of delivering the intervention and this treatment's impact on subsequent use and cost of health services. We also will include indirect costs to participants and their families due to their participation in the intervention and use of other health care services (e.g., time spent in travel, usual care visits, out-of session activities).
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Healthy lifestyle intervention
lifestyle/weight-loss intervention for overweight (95th - 99th percentile) female adolescents (13-15 years of age at study entry) to a usual-care control condition. The intervention will be 20-sessions and combines group visits, individual telephone coaching calls, and tailored pediatric primary care providers (PCP) visits.
Healthy lifestyle managment
Exercise, yoga, food diaries, provider consultation
Usual care
In the usual care control condition adolescents and their family will receive individualized feedback from the assessments as well as handouts outlining healthy means of maintaining / reducing weight for adolescents through improving nutrition and physical activity. In addition, these participants will be encouraged to seek any appropriate health care/education services available through Kaiser Permanente or in the community.
No interventions assigned to this group
Interventions
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Healthy lifestyle managment
Exercise, yoga, food diaries, provider consultation
Eligibility Criteria
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Inclusion Criteria
* Ages 13- 15 at study recruitment,
* BMI in overweight range (95th percentile - 99th percentile,
* One or both parent(s) willing to participate.
Exclusion Criteria
* Significant cognitive impairment,
* Current pregnancy,
* Congenital heart disease that limits activity,
* Serious asthma requiring oral prednisone,
* Taking medications that increase appetite.
13 Years
15 Years
FEMALE
Yes
Sponsors
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Kaiser Permanente
OTHER
Responsible Party
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Kaiser Permanente
Principal Investigators
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Victor J Stevens, PhD
Role: PRINCIPAL_INVESTIGATOR
Kaiser Permanente
References
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DeBar LL, Stevens VJ, Perrin N, Wu P, Pearson J, Yarborough BJ, Dickerson J, Lynch F. A primary care-based, multicomponent lifestyle intervention for overweight adolescent females. Pediatrics. 2012 Mar;129(3):e611-20. doi: 10.1542/peds.2011-0863. Epub 2012 Feb 13.
Other Identifiers
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NCT00451685
Identifier Type: -
Identifier Source: nct_alias
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