Pediatric Obesity — Adapting Diet and Action for Everyone (ADAPT+)
Citation(s)
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Dahmer S Do you have any advice on how to help with this problem of access to CAM therapies for patients without financial resources? Explore (NY). 2007 Sep-Oct;3(5):546. doi: 10.1016/j.explore.2007.07.013. No abstract available.
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Daly P, Pace T, Berg J, Menon U, Szalacha LA A mindful eating intervention: A theory-guided randomized anti-obesity feasibility study with adolescent Latino females. Complement Ther Med. 2016 Oct;28:22-8. doi: 10.1016/j.ctim.2016.07.006. Epub 2016 Aug 1.
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Halperin DT, Laux J, LeFranc-Garcia C, Araujo C, Palacios C Findings From a Randomized Trial of Weight Gain Prevention Among Overweight Puerto Rican Young Adults. J Nutr Educ Behav. 2019 Feb;51(2):205-216. doi: 10.1016/j.jneb.2018.07.014. Epub 2018 Oct 2.
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Martinez SM, Rhee K, Blanco E, Boutelle K Maternal attitudes and behaviors regarding feeding practices in elementary school-aged Latino children: a pilot qualitative study on the impact of the cultural role of mothers in the US-Mexican border region of San Diego, California. J Acad Nutr Diet. 2014 Feb;114(2):230-237. doi: 10.1016/j.jand.2013.09.028. Epub 2013 Dec 4.
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Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.
Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.
Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.
Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.
Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.