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EXERT-BCN: An Exercise and Nutrition Regimen to Designed to Improve Body Composition After Treatment for Breast Cancer (EXERT-BCN)

Primary Purpose

Breast Cancer

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Nutrition and resistance training exercise intervention
Sponsored by
Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Breast Cancer focused on measuring breast cancer, nutrition, body composition

Eligibility Criteria

20 Years - 89 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Age 20-89 years Women with a biopsy proven diagnosis of ductal carcinoma in situ or invasive carcinoma of the breast. Women must have undergone treatment for breast cancer, including one or more of the following: surgery, radiation therapy, chemotherapy, immunotherapy, or hormonal therapy. Women undergoing active chemotherapy are not allowed on study. Treatment with targeted agents and immunotherapy is allowed. Exclusion Criteria: Any current treatment with chemotherapy for breast cancer Inability to get and down off the ground or squat body weight Inability to safely engage in group sessions Severe arthritic, joint, cardiovascular, or musculoskeletal condition deemed by PI to be unsafe to engage in resistance training

Sites / Locations

  • AHN CI Exercise Oncology and ResiliencyRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Resistance training with high quality low-carbohydrate nutrition regimen

Arm Description

The regimen will consist of an intense resistance training program with linear progression and the goal of increase strength, mobility, muscle mass, and functional capacity. The nutrition program will avoid calorie counting, and instead focus on quality, while maximizing protein and limiting carbohydrates.

Outcomes

Primary Outcome Measures

Determine changes in fat mass in pounds from before to after the nutrition and exercise regimen via bioimpedance analysis
Measurement on bioimpedance analysis machine (Inbody 970)
Determine changes in fat mass in pounds from before to after the nutrition and exercise regimen via ultrasound
Measurement via ultrasound and calculation with Jackson-Pollack calculations

Secondary Outcome Measures

Determine changes in bone mineral concentration in pounds from before to after the nutrition and exercise regimen
Measurement on bioimpedance analysis machine (Inbody 970)
Determine changes in GAD7 anxiety score from before to after the nutrition and exercise regimen
GAD7 asks 8 questions rated from 0 to 3
Determine changes in PHQ9 depression score from before to after the nutrition and exercise regimen
PHQ9 asks 10 questions rated from 0 to 3
Determine changes in EQ-5D responses 1-5 and overall score from before to after the nutrition and exercise regimen
EQ-5D asks 5 questions rates from 1-5 and an overall rating of health
Determine changes in strength via load measured in pounds from before to after the nutrition and exercise regimen
Load is calculated by multiplying sets by repetitions by weight lifted for a specific exercise
Determine changes in Y-balance score for each leg
Y-balance score adds up the distance each leg can move in the front and side directions, divided by the length of the hip. This correlates inversely with fall risk.
Determine changes in overall score of functional movement screen (FMS) from before to after the nutrition and exercise regimen
Functional movement screen (FMS) is a 7 movement test where an individual can score from 0 to 21
Determine changes in resting metabolic rate in kilocalories/day from before to after the nutrition and exercise regimen
Measurement via VO2 Master indirect calorimeter
Determine changes in muscle mass in pounds from before to after the nutrition and exercise regimen
Measurement on bioimpedance analysis machine (Inbody 970)

Full Information

First Posted
July 31, 2023
Last Updated
July 31, 2023
Sponsor
Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)
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1. Study Identification

Unique Protocol Identification Number
NCT05978960
Brief Title
EXERT-BCN: An Exercise and Nutrition Regimen to Designed to Improve Body Composition After Treatment for Breast Cancer
Acronym
EXERT-BCN
Official Title
An EXErcise Regimen Designed to Improve Body Composition, Functional Capacity, and Strength After Treatment for Breast Cancer With Nutrition Optimization
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 20, 2023 (Actual)
Primary Completion Date
May 20, 2024 (Anticipated)
Study Completion Date
August 20, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This protocol seeks to analyze patient outcomes of the standard of care, monitored group exercise regimen of high-load resistance training and functional exercises with compound movements in conjunction with a nutrition regimen focused on food quality under close supervision on women who have been treated for breast cancer.
Detailed Description
Excess adipose tissue is a risk factor for the diagnosis of breast cancer and is also associated with an increased risk of disease recurrence.1 Additionally weight gain during and after treatment for breast cancer is associated with a higher risk of recurrence, distant metastases, and death.2 More specifically, low muscle mass and increased adipose tissue is associated with poorer outcomes after the treatment of breast cancer.3 Yet, most women gain significant weight during and after breast cancer treatment, potentially compromising outcomes. Effective methods to promote weight loss and improve metabolic and hormonal dysregulation, inflammation, and body composition in the breast cancer setting are urgently needed. In the noncancer setting, the promotion of high-quality diets that avoided processed food and simple carbohydrates in the DIETFITS study promoted weight loss4. However, this dietary strategy and others were utilized to result in weight loss, but do not necessarily consider maximizing body composition, i.e., muscle mass preservation or increase, and adipose tissue loss. The major, and some would consider only, non-pharmacological method to increase muscle mass is via resistance training with an adequate stimulus and quantity to elicit and promote hypertrophy.5 Our group has already shown that profound muscle hypertrophy is attainable in a population of women undergoing treatment for breast cancer, particularly when the dose threshold of load and repetitions is met. At interim analysis, this program revealed a 2 lb. increase in muscle mass and a 6 lb. decrease in adipose tissue after a 3 month program utilizing linear progression. Based on the DIEFITS protocol which has been described as a "healthy low-carbohydrate" diet, participants will be advised to eat nutrient dense food sources high in vitamins, minerals, and nutrients. Participants will be told to limit processed foods, sugar, bread, pasta, and other simple carbohydrates. Participants will be advised to eat plenty of colorful and nonstarchy vegetables. Finally, participants will be told to avoid snacking between meals, cook most/all meals, eat with family and friends, avoid eating food in the car or on the run, and focus on whole foods that require preparation. This protocol resulted in significant weight loss at one year. Additionally, the lack of calculations and quantification of calories leaves this as a more user-friendly option for participants. The exercise regimen from EXERT-BC has yet to be combined with a dietary intervention. Thus, the following protocol will assess our resistance training regimen in conjunction with a nutrition intervention similar to the DIETFITS Protocol. This will allow adequate assessment of whether we can optimize body composition in these individuals with both exercise and dietary changes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
breast cancer, nutrition, body composition

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
44 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Resistance training with high quality low-carbohydrate nutrition regimen
Arm Type
Experimental
Arm Description
The regimen will consist of an intense resistance training program with linear progression and the goal of increase strength, mobility, muscle mass, and functional capacity. The nutrition program will avoid calorie counting, and instead focus on quality, while maximizing protein and limiting carbohydrates.
Intervention Type
Other
Intervention Name(s)
Nutrition and resistance training exercise intervention
Intervention Description
3 month 2-3 times/week, 60 min exercise regimen utilizes compound movements to focus on body composition, strength, and mobility. Classes are run by certified strength and conditioning specialists and adjusted for linear progression and safety, progressing from compound to isolated movements to maximize safety. The nutrition intervention focuses on dietary quality by following a "healthy low-carbohydrate" diet, focusing on nutrient dense foods high and avoiding processed foods and simple carbohydrates to keep totals under 100g/day. Participants will be advised to eat vegetables, avoid snacking, cook all meals with family and friends, avoid eating on the run, and focus on whole foods that require preparation. Calculations and quantification of calories will be avoided, while protein consumption goals are 1.3-1.8 g/kg per. Dietary strategy will be continuously discussed during exercise sessions and the PI will have twice monthly meetings with participants.
Primary Outcome Measure Information:
Title
Determine changes in fat mass in pounds from before to after the nutrition and exercise regimen via bioimpedance analysis
Description
Measurement on bioimpedance analysis machine (Inbody 970)
Time Frame
3 months
Title
Determine changes in fat mass in pounds from before to after the nutrition and exercise regimen via ultrasound
Description
Measurement via ultrasound and calculation with Jackson-Pollack calculations
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Determine changes in bone mineral concentration in pounds from before to after the nutrition and exercise regimen
Description
Measurement on bioimpedance analysis machine (Inbody 970)
Time Frame
3 months
Title
Determine changes in GAD7 anxiety score from before to after the nutrition and exercise regimen
Description
GAD7 asks 8 questions rated from 0 to 3
Time Frame
3 months
Title
Determine changes in PHQ9 depression score from before to after the nutrition and exercise regimen
Description
PHQ9 asks 10 questions rated from 0 to 3
Time Frame
3 months
Title
Determine changes in EQ-5D responses 1-5 and overall score from before to after the nutrition and exercise regimen
Description
EQ-5D asks 5 questions rates from 1-5 and an overall rating of health
Time Frame
3 months
Title
Determine changes in strength via load measured in pounds from before to after the nutrition and exercise regimen
Description
Load is calculated by multiplying sets by repetitions by weight lifted for a specific exercise
Time Frame
3 months
Title
Determine changes in Y-balance score for each leg
Description
Y-balance score adds up the distance each leg can move in the front and side directions, divided by the length of the hip. This correlates inversely with fall risk.
Time Frame
3 months
Title
Determine changes in overall score of functional movement screen (FMS) from before to after the nutrition and exercise regimen
Description
Functional movement screen (FMS) is a 7 movement test where an individual can score from 0 to 21
Time Frame
3 months
Title
Determine changes in resting metabolic rate in kilocalories/day from before to after the nutrition and exercise regimen
Description
Measurement via VO2 Master indirect calorimeter
Time Frame
3 months
Title
Determine changes in muscle mass in pounds from before to after the nutrition and exercise regimen
Description
Measurement on bioimpedance analysis machine (Inbody 970)
Time Frame
3 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
89 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 20-89 years Women with a biopsy proven diagnosis of ductal carcinoma in situ or invasive carcinoma of the breast. Women must have undergone treatment for breast cancer, including one or more of the following: surgery, radiation therapy, chemotherapy, immunotherapy, or hormonal therapy. Women undergoing active chemotherapy are not allowed on study. Treatment with targeted agents and immunotherapy is allowed. Exclusion Criteria: Any current treatment with chemotherapy for breast cancer Inability to get and down off the ground or squat body weight Inability to safely engage in group sessions Severe arthritic, joint, cardiovascular, or musculoskeletal condition deemed by PI to be unsafe to engage in resistance training
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Samantha Campbell
Phone
(412) 330-6151
Email
samantha.campbell@ahn.org
Facility Information:
Facility Name
AHN CI Exercise Oncology and Resiliency
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15202
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Colin E Champ
Phone
412-734-7605
Email
colin.champ@ahn.org
First Name & Middle Initial & Last Name & Degree
Colin E Champ, MD, CSCS
First Name & Middle Initial & Last Name & Degree
Christopher L Peluso, MS, CSCS
First Name & Middle Initial & Last Name & Degree
Christie Hilton, DO

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Undecided at this point
Citations:
PubMed Identifier
29466592
Citation
Gardner CD, Trepanowski JF, Del Gobbo LC, Hauser ME, Rigdon J, Ioannidis JPA, Desai M, King AC. Effect of Low-Fat vs Low-Carbohydrate Diet on 12-Month Weight Loss in Overweight Adults and the Association With Genotype Pattern or Insulin Secretion: The DIETFITS Randomized Clinical Trial. JAMA. 2018 Feb 20;319(7):667-679. doi: 10.1001/jama.2018.0245. Erratum In: JAMA. 2018 Apr 3;319(13):1386. JAMA. 2018 Apr 24;319(16):1728.
Results Reference
background
PubMed Identifier
36175646
Citation
Champ CE, Carpenter DJ, Diaz AK, Rosenberg J, Ackerson BG, Hyde PN. Resistance Training for Patients with Cancer: A Conceptual Framework for Maximizing Strength, Power, Functional Mobility, and Body Composition to Optimize Health and Outcomes. Sports Med. 2023 Jan;53(1):75-89. doi: 10.1007/s40279-022-01759-z. Epub 2022 Sep 29.
Results Reference
background

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EXERT-BCN: An Exercise and Nutrition Regimen to Designed to Improve Body Composition After Treatment for Breast Cancer

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