- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01542216
Evaluation of Nutrition and Metabolism in Breast Cancer Patients
4. november 2015 opdateret af: University of Waterloo
With the increased success in breast cancer therapies, survivors develop unhealthy changes in body composition, such as muscle loss and fat gains, which lead to increased risk of cardiovascular disease and diabetes in survivorship.
This study will examine the effects of a nutrition, cardiovascular and strength exercise program compared with a yoga program (representing usual care) on body composition and metabolism in recently diagnosed breast cancer patients.
Nutrition and exercise may improve various body composition and metabolic parameters, which may improve quality of life in survivorship, reduce risk of recurrence and reduce the risk of developing cardiovascular disease and diabetes in survivorship.
Studieoversigt
Status
Trukket tilbage
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Despite the increased success of novel anti-neoplastic therapies, breast cancer patients receiving chemotherapy develop unfavourable changes in body composition, including lean tissue loss and fat gains (1,2).
These detrimental changes associate with poor quality of life (3,4) and may lead to treatment complications (5,6) during the cancer trajectory.
In non-malignant populations, fat gain and muscle loss associate with increased risk of cardiovascular disease and diabetes (7).
Cancer survivors who gain fat and lose lean mass are not only predisposed to these diseases but also have an increased risk of cancer recurrence (3).
Proper nutrition as well as exercise can independently improve metabolic profiles (i.e.
immune function, lipid and glucose metabolism) and overall health outcomes in non-malignant populations (7-9).
While exercise has enhanced quality of life in breast cancer patients (4), overall nutritional needs and the metabolic benefits of exercise are unclear in this patient group.
Understanding the effects of nutrition and exercise interventions in breast cancer patients will form the basis for future studies and programs that integrate nutrition, exercise, and metabolism to reduce cancer recurrence and other morbidities in survivorship.
This study will examine the effects of nutrition and exercise intervention on body composition and metabolism in recently diagnosed breast cancer patients.
Undersøgelsestype
Interventionel
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Ontario
-
Waterloo, Ontario, Canada, N2L 3G1
- University of Waterloo
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Kvinde
Beskrivelse
Inclusion Criteria:
- Females 18 years old or older
- Recent diagnosis of breast cancer and up to 4 weeks following the first cycle of chemotherapy or up to the first 4 weeks of radiation therapy
- Clinical Stages I-IIIa
- Able to communicate freely in English
- Have sufficient cognitive ability to participate and provide informed consent
Exclusion Criteria:
- Any known diagnosis of cardiovascular disease and thyroid disease that is not currently managed with medication or other therapies
- Any known diagnosis of diabetes or HIV
- Pre-existing injuries or health conditions that prevents the patient's safe participation in exercise
- Any previous diagnosis of cancer within the last 5 years (other than carcinoma in situ)
- Fasting glucose >7.0 mM at baseline of the study
- Pregnant individuals will be excluded from this study
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Støttende pleje
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Placebo komparator: Yoga and Stretching Group
Patients undergo yoga and stretching exercises
|
Patients randomized to this arm will receive consultations on yoga and stretching exercises.
Andre navne:
|
|
Aktiv komparator: Nutrition and Exercise Group
Patients are provided with nutrition, cardiovascular exercise and strength exercise consultations
|
Patients randomized to this arm will receive nutrition and exercise consultations.
Exercise consultations will home- and institution-based.
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in glucose parameters from baseline
Tidsramme: Baseline, 8 weeks, 16 weeks
|
Oral glucose tolerance tests will be performed at each assessment.
Changes from baseline will be measured.
|
Baseline, 8 weeks, 16 weeks
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Change in lipid profile relative to baseline
Tidsramme: Baseline, 8 weeks, 16 weeks
|
Baseline, 8 weeks, 16 weeks
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Marina Mourtzakis, PhD, University of Waterloo
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. februar 2012
Primær færdiggørelse (Forventet)
1. juni 2015
Studieafslutning (Forventet)
1. september 2015
Datoer for studieregistrering
Først indsendt
20. februar 2012
Først indsendt, der opfyldte QC-kriterier
24. februar 2012
Først opslået (Skøn)
2. marts 2012
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
5. november 2015
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
4. november 2015
Sidst verificeret
1. november 2015
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 17215
- 2011-0463 (Anden identifikator: Tri-Hospital Research Ethics Board)
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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