THRIVE Well Cancer FDTN/Exercise_Creatine Supplementation
- Conditions
- Breast Cancer FemaleMuscle WeaknessBreast Cancer
- Registration Number
- NCT06395506
- Brief Summary
The study's purpose is to evaluate whether creatine supplementation can help breast cancer survivors respond quicker to exercise by improving strength, endurance, and body composition. We are seeking to compare information collected from healthy woman of the same age who have never had breast cancer to those participants who have had breast cancer and undergone chemotherapy treatment.
- Detailed Description
The primary objective of this study is to determine the effects of creatine supplementation in modulating strength and physical function in breast cancer survivors that have recently completed chemotherapy. The primary objective is to determine the effects of creatine in modulating strength and physical function in cancer survivors.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Female
- Target Recruitment
- 60
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Change in physical functional capacity in breast cancer survivors baseline and 12 weeks Determine the change in strength in breast cancer survivors by comparing pre and post measurements of the six minute walk test.
Change in strength in breast cancer survivors baseline and 12 weeks Determine the change in strength in breast cancer survivors by comparing pre and post measurements of strength measurement tools including 1RM/10RM/Biodex evaluations.
- Secondary Outcome Measures
Name Time Method Change intramuscular storage of creatine baseline and 12 weeks Determine the change in intramuscular storage of creatine by comparing pre and post vastus lateralis muscle using MRI.
Change in the return of strength for breast cancer survivors with creatine + exercise 12 weeks Breast cancer survivors who complete 12-weeks of exercise with creatine supplementation group who regained strength and physical function to that of women of similar age who never had cancer.
Change in body composition in cancer survivors baseline and 12 weeks Determine the change in body composition in breast cancer survivors by pre and post measurements of bone mass as well as lean vs fat mass via a DEXA scan.
Related Research Topics
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Trial Locations
- Locations (1)
The University of Texas Medical Branch, Galveston
🇺🇸Galveston, Texas, United States
The University of Texas Medical Branch, Galveston🇺🇸Galveston, Texas, United StatesLisa Thibodeaux, RN,BSNContact409-474-1756lbthibod@utmb.eduRebecca Geck, MPH,APRN,CPTContact4092660496raschaef@utmb.edu