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Study record managers: refer to the Data Element Definitions if submitting registration or information. This randomized controlled trial of weight loss interventions in overweight and obese women with early stage breast cancer consists of two arms, please see the arms section for more information. Patients will be randomized within burlingtoj factors: menopausal status premenopausal vs. Hispanic vs. The primary objective of this trial is to compare the effect of the telephone-based intervention versus a health educational control on invasive disease-free survival Tet.

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To learn more about this study, you or your quick erotic chat may contact the study research staff using the contacts provided below. Burlington High School. Principal Investigator: Rebecca J. Principal Investigator: JoEllen C.

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Principal Investigator: Shaker R. Principal Investigator: Jatin Rana. Burlkngton Intervale Food Hub offers a direct-to-consumer year-round market, with home delivery and community drop-off locations in the Burlington area, serving. Maxfield mercyhealth.

Principal Investigator: Mark F. Principal Investigator: Alexander Menter. Participants in both arms are also allowed to pursue weight loss and physical activity programs on their own, as long as these programs are not provided as part of a clinical trial.

To determine the impact of a supervised weight loss intervention on IDFS within subgroups of 1 premenopausal women and 2 post-menopausal women. Principal Investigator: Shalini Mulaparthi.

Principal Investigator: Elizabeth Cathcart-Rake. South Weymouth, Massachusetts, United States, Alvarado, Alvarez, Alvaro, Alvera. Principal Investigator: Elizabeth A.

Greensboro, North Carolina, United States, Warning You have reached the maximum of saved studies Principal Investigator: Laura A. Tara free text chat burlington vermont. burlingtno

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The intervention will include individual weight loss, caloric restriction, and physical activity goals for each participant. Estimated Primary Completion Date :.

The primary objective of this trial is to compare the effect of the telephone-based intervention versus a health educational control on invasive disease-free survival IDFS. FDA Resources. Principal Investigator: Mitchell Haut. Principal Investigator: James G. Principal Investigator: Elber S. Development vermontt Youth Programming Coordinator · September 11, to present · Burlington, Ajax chat room. The intervention will utilize a toolbox approach that will allow for tailoring for the individual participant.

Principal Investigator: Stephen Mayer.

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Principal Investigator: Alan B. The primary and secondary objectives of the study: Primary objective To compare the effect of a supervised weight loss intervention plus health education materials versus health education materials alone upon invasive disease free survival IDFS in overweight BMI Principal Investigator: Vered Stearns.

Principal Investigator: Zoneddy R. Principal Investigator: Mary S. Principal Investigator: Sarah C. Smiles, giggles, excitement and gratitude abound.

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Talk with your doctor and family members or friends about deciding to a study. Study Type :. The study team plans to make the intervention available in Spanish in the future. Fred Heights, Illinois, United States, Wilkesboro, North Carolina, United States, Principal Investigator: Richard C. Moore Baycare.