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Diet Composition, Weight Control, and Breast Carcinogenesis (CHOICE)

13 lutego 2013 zaktualizowane przez: Henry J. Thompson, Colorado State University

In the United States, overweight (BMI > 25 but < 30 Kg/m2) and obesity (BMI > 30Kg/m2) are increasing at epidemic rates. A significant association exists between being overweight or obese and breast cancer recurrence and survival. However, evidence continues to accumulate indicating that achieving or maintaining a healthy weight for height (Body Mass Index, BMI, 18.5-25Kg/m2) is associated with a reduced risk for breast cancer and with a decrease in breast cancer associated mortality. Despite this, there is a lack of randomized controlled trials exploring this association and how the process of fat loss or being successful in actually reaching a healthy weight for height differentially affects biomarkers for cancer recurrence.

Many dietary approaches for weight loss are currently available to the public, and each purports to offer advantages. However, there is little scientific evidence to indicate how these dietary approaches, some of which vary markedly in the foods that they limit or exclude, affect biomarkers for breast cancer risk. In particular, it is not know whether the critical factor in relation to weight and breast cancer is simply weight loss (negative energy balance), irrespective of the manner in which it is achieved, or if certain dietary approaches affect breast cancer risk biomarkers more favorably than others. Published data from our laboratory suggest that dietary pattern does matter, and therefore the goal of this study is to investigate the effects of two popular weight loss dietary approaches that differ in the extent to which they limit carbohydrate or fat consumption (with effects on dietary glycemic load) compared to a usual care group on prognostic markers for cancer recurrence in postmenopausal breast cancer survivors. The investigators hypothesize that in addition to the anticipated effects of fat loss on circulating levels of bioavailable sex steroid hormones, that the effects of excess fat on breast cancer prognosis can be attributed to three interrelated metabolic processes that affect cancer progression: altered glucose metabolism, chronic inflammation and excessive cellular oxidation.

Przegląd badań

Status

Zakończony

Warunki

Szczegółowy opis

This study is designed to answer questions about how a dietary pattern either high or low in dietary carbohydrate and fat availability and fat loss influence metabolic and hormonal processes that may affect breast cancer recurrence. The investigators hypothesize that in addition to the anticipated effects of fat loss on circulating levels of bioavailable sex steroids, that the effects of excess fat on breast cancer prognosis can be attributed to three interrelated metabolic processes: altered glucose metabolism (IGF-1, IGFBP-3, glycated proteins), chronic inflammation (C-reactive protein, IL-6, TNF-alpha) and excessive cellular oxidation (8-hydroxy-2-deoxyguanosine and 8-isoprostane F-2 alpha).

A 6 month intervention study involving 370 post menopausal women who have been treated for breast cancer is proposed. Randomized women, stratified by resected stage, systemic adjuvant therapy and body mass index (> 25 and < 35 Kg/m2), will serve as either a non-intervention control group or will follow a tailored diet-physical activity program designed to create a weekly negative energy balance equivalent to 3500 kcal. The intervention groups will receive the same physical activity protocol, but one of two diets that differ in dietary pattern.

The specific aims are: Aim 1. Does a dietary pattern either high or low in available carbohydrate and fat alter the pattern of change observed in circulating factors involved in glucose homeostasis, chronic inflammation, cellular oxidation, and steroid hormone metabolism during progressive loss of body fat? The investigators will also examine how observed changes in these circulating factors related to changes indicators of breast cancer recurrence. Aim 2. Do circulating factors associated with glucose homeostasis, chronic inflammation, and cellular oxidation display the same pattern of change in response to progressive fat loss as circulating analytes associated with sex steroid metabolism? Analytes of interest will be measured monthly throughout the study. Aim 3. Does dietary glycemic load affect the magnitude or rate of fat loss? Plasma adipokines such as leptin and adiponectin and plasma ghrelin will be measured to provide biological determinants that may help explain differences in response.

The work proposed in this application should provide quantitative data about the importance of the magnitude of fat loss on metabolic and hormonal processes involved in cancer recurrence and provide guidance about effective dietary approaches that maximize weight loss benefits on breast cancer prognosis.

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

259

Faza

  • Nie dotyczy

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

    • Colorado
      • Denver, Colorado, Stany Zjednoczone, 80220
        • Rocky Mountain Cancer Center

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

21 lat i starsze (Dorosły, Starszy dorosły)

Akceptuje zdrowych ochotników

Tak

Płeć kwalifikująca się do nauki

Kobieta

Opis

Inclusion Criteria:

  • Female breast cancer survivors
  • Staged, resected breast cancer (> 4-months post radiation treatment, chemotherapy or surgery)
  • Post-menopausal (no menses for > 6 months)
  • No evidence of metastatic breast disease
  • Willing to follow the diet plan prescribed
  • Willing to follow the guidelines for alcohol consumption (no more than 1 standard alcoholic drink per day where one serving is defined as 12oz beer, 5 oz wine OR 1 oz hard liquor)
  • Willing to maintain or increase current physical activity level
  • Willing to wear a pedometer and keep a daily record of steps
  • Willing to wear heart rate/ accelerometer device (Actiheart) continuously (24/7) for one week at the start and end of the study
  • Willing to wear a body or swim suit and cap for body composition tests
  • Willing to record food intake daily
  • Willing to come to RMCC Rose for 11 individual and 5 group sessions over a 6 month period
  • Willing to provide urine and fasting blood samples at 7 visits during the study
  • Willing to make the commitment it takes to lose weight for the study
  • Must have a Body Mass Index between 25Kg/m2 to 35Kg/m2.

Exclusion Criteria:

  • Anticipates having surgery during the next 6 months
  • Follows a special diet, e.g. gluten free, casein free, dairy free, vegetarian or other
  • Lost 4 or more pounds during the previous month
  • Taking weight loss medications during the study
  • Being treated by a physician for diabetes
  • Has an eating disorder
  • Has digestive problems such as IBS (Irritable Bowel Syndrome), Crohn's or other
  • Has had surgery involving constriction or removal of any portion of the gastrointestinal tract (gastric bypass, lap-band, bowel resection, colostomy etc.
  • Diagnosed with hepatitis B, hepatitis C or HIV
  • Has electronic devices implanted in their body (pacemaker, vagus nerve stimulator)
  • Must not use any tobacco products

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Zapobieganie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Pojedynczy

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Brak interwencji: Kontrola
Zwykła opieka
Eksperymentalny: Low fat, high carb weight loss diet
Ornish-like weight loss dietary pattern
Diet-physical activity program creating a weekly negative energy balance equivalent to 3500 kcal. Intervention groups receive PA protocol promoting the Physical Activity Guidelines and translated in step recommendations, but one of two diets with divergent dietary patterns (opposing fat and CHO content) that do not overlap >+5% in CHO and fat content. Macronutrient values reflect a 'pattern' or ratio within (LC 3:2 ratio for F:CHO; HC 1:4 ratio for F:CHO ) and between diets (LC:HC 3:1 for fat; LC:HC 1:2 for CHO). Six-week meal plans for five calorie levels available and incorporate educational material, supporting program components (e.g. self monitoring tools) and core competencies reinforcing weight loss behaviors in order to promote high levels of dietary adherence.
Inne nazwy:
  • Low fat, high carb weight loss diet (Vivace Diet)
  • Low carb, high fat weight loss diet (Ricca Diet)
Eksperymentalny: Low carb, high fat weight loss diet
South-Beach-like weight loss diet pattern
Diet-physical activity program creating a weekly negative energy balance equivalent to 3500 kcal. Intervention groups receive PA protocol promoting the Physical Activity Guidelines and translated in step recommendations, but one of two diets with divergent dietary patterns (opposing fat and CHO content) that do not overlap >+5% in CHO and fat content. Macronutrient values reflect a 'pattern' or ratio within (LC 3:2 ratio for F:CHO; HC 1:4 ratio for F:CHO ) and between diets (LC:HC 3:1 for fat; LC:HC 1:2 for CHO). Six-week meal plans for five calorie levels available and incorporate educational material, supporting program components (e.g. self monitoring tools) and core competencies reinforcing weight loss behaviors in order to promote high levels of dietary adherence.
Inne nazwy:
  • Low fat, high carb weight loss diet (Vivace Diet)
  • Low carb, high fat weight loss diet (Ricca Diet)

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Inflammation Markers
Ramy czasowe: Baseline and montlhly for 6 months
C-reactive protein, IL-6, TNF-alpha
Baseline and montlhly for 6 months

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Body Fat Percentage (%)
Ramy czasowe: Baseline and monthly for 6 months
% Body fat, % lean muscle mass, Resting Metabolic Rate (RMR) using the BODPOD (Volumetric weighing; Life Measurement, Inc.) and Tanita Bioelectrical Impedence (BI)
Baseline and monthly for 6 months
Waist Hip Ratio
Ramy czasowe: Baseline and monthly for 6 months
Calculated by measuring and dividing waist and hip circumferences
Baseline and monthly for 6 months
Weight
Ramy czasowe: Baseline and monthly for 6 months
Using 1) BODPOD (Life Measurement, Inc.) and 2) Tanita Bioelectrical Impedence Scale
Baseline and monthly for 6 months
Bioavailable sex steroid hormones
Ramy czasowe: Baseline and monthly for 6 months
estradiol, estrone, sex hormone binding globulin (SHBG)
Baseline and monthly for 6 months
Glucose metabolism
Ramy czasowe: Baseline and monthly for 6 months
glucose, insulin, IGF-1, IGFBP-3, glycated proteins (HbA1c)
Baseline and monthly for 6 months
Cellular oxidation
Ramy czasowe: Baseline and monthly for 6 months
8-hydroxy-2-deoxyguanosine, DNA damage sensitivity and repair and 8-isoprostane-F-2-alpha
Baseline and monthly for 6 months

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Śledczy

  • Główny śledczy: Henry J Thompson, PhD, Colorado State University
  • Główny śledczy: Scot M Sedlacek, MD, Rocky Mountain Cancer Center

Publikacje i pomocne linki

Osoba odpowiedzialna za wprowadzenie informacji o badaniu dobrowolnie udostępnia te publikacje. Mogą one dotyczyć wszystkiego, co jest związane z badaniem.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów

1 września 2008

Zakończenie podstawowe (Rzeczywisty)

1 stycznia 2012

Ukończenie studiów (Rzeczywisty)

1 czerwca 2012

Daty rejestracji na studia

Pierwszy przesłany

14 marca 2011

Pierwszy przesłany, który spełnia kryteria kontroli jakości

14 marca 2011

Pierwszy wysłany (Oszacować)

15 marca 2011

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Oszacować)

15 lutego 2013

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

13 lutego 2013

Ostatnia weryfikacja

1 lutego 2013

Więcej informacji

Terminy związane z tym badaniem

Inne numery identyfikacyjne badania

  • CA125243

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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