Exercise in Metastatic Breast Cancer: EMBody

Breast Cancer Clinical Trial

Official title:

Exercise in Metastatic Breast Cancer: EMBody

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05468034
• Other study ID #: CTO-IUSCCC-0781
• Status: Recruiting
• Phase: N/A
• Start date: April 26, 2023
• Est. completion date: December 2027

Study information

• Verified date: June 2024
• Source: Indiana University
• Contact: Jackson Richey
• Phone: 317-274-0922
• Email: jaerich[@]iupui.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to study exercise in a novel population with indolent MBC (no progression on current therapy in prior 12 months and not receiving cytotoxic chemotherapy). The study team hypothesizes that delivering virtual, supervised, progressive intensity aerobic and resistance training exercise for 16 weeks in this population will significantly improve 1) cardiorespiratory fitness, functional status, and sarcopenia (low muscle mass), all established predictors of survival, and 2) patient- reported outcomes.

Description:

This is a randomized, two arm, single-center study designed to compare the effect of exercise versus usual care control on the clinical parameter of cardiorespiratory fitness, in patients with metastatic breast cancer with indolent disease biology over a 16-week period. This study will be enrolling up to 100 participants. Participants will be randomized 1:1 in blocks of 4 to the exercise intervention or usual care, stratified by frailty yes/no defined by baseline SPPB score ≤ 8 or > 8.

Primary Objective To compare the effect of a 16-week multimodality, virtually delivered exercise intervention on cardiorespiratory fitness measured by a modified Bruce ramp protocol treadmill test to usual care, in patients with indolent metastatic breast cancer.

Secondary Objectives

1. To compare the effect of exercise versus usual care on objective physical function measured by the short physical performance battery (SBBP)

2. To compare the effect of exercise versus usual care on subjective physical functioning measured by PROMIS-29 questionnaire

3. To compare the effect of exercise versus usual care on body composition, measured by visceral adiposity, lean muscle mass, and muscle density on CT scans obtained as standard of care using SliceOmatic software

4. To compare the effect of exercise versus usual care on objective physical activity measured by accelerometer wear

5. To compare the effect of exercise versus usual care on patient reported outcomes, including fatigue (BFI) and health related quality of life (PROMIS-29)

6. To determine the fidelity of the exercise intervention, measured by changes in measures of constructs of habit and intention administered by questionnaire

7. To describe patient uptake and adherence with the intervention, measured by proportion of approached patients who consent to the study, and proportion of assigned training sessions attended by patients randomized to the exercise arm.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 100
• Est. completion date: December 2027
• Est. primary completion date: December 2027
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Age = 18 years

2. Diagnosis of metastatic breast cancer

3. No progression of disease in the 12 months prior to screening per the treating investigator

1. If participant has changed treatments in the prior 12 months for reasons other than progressive disease, they remain eligible

2. Participants on no treatment or "no evidence of disease" but still with a diagnosis of metastatic breast cancer are eligible

4. ECOG performance status of 0-2

5. Ability to walk on a treadmill without assistive device.

6. Informed consent and authorization of the release of health information must be obtained according to institutional guidelines

7. Currently not meeting physical activity guidelines (defined as less than 150 minutes of moderate to vigorous exercise per week measured by the RPAQ questionnaire administered during screening)

8. Participants should have a cellular device compatible with iOS 15 or Android operating system 7.

Exclusion Criteria:

1. Receiving cytotoxic chemotherapy at any point in the prior 12 months.

1. Participants receiving endocrine therapy are eligible.

2. Participants receiving targeted therapy or antibody therapy are eligible (examples including trastuzumab, pertuzumab, TDM-1, trastuzumab deruxtecan, sacituzumab govetecan, immunotherapy, CDK4/6 inhibitors, olaparib, alpelisib, etc.)

2. Any condition precluding supervised exercise participation. A letter from a physician supporting participation can supercede this eligibility criteria.

• NYHA class III or IV congestive heart failure

• Uncontrolled angina

• Myocardial infarction in the prior 12 months

• Orthopedic surgery in the previous 3 months or plans for orthopedic surgery during the study period

• Chronic uncontrolled pulmonary conditions such as uncontrolled asthma (symptoms > 2 days/week) or dyspnea requiring oxygen

• Symptomatic peripheral vascular disease

• Or any other comorbidity that would interfere with the ability to complete and comply with the protocol in the opinion of the investigator, including psychological illness

• History of fragility fracture

3. Active, untreated brain metastases

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Behavioral:
• Exercise Intervention
Eligible and consented participants randomized to the exercise arm (EX) will work with an exercise trainer 3x weekly for 16 weeks. Training sessions are 60 min. Schedules are determined by participant and trainer with oversight by the study team, ideally occurring at similar times each day in line with IBC theory. Each training session will be delivered virtually over a HIPAA compliant IU Health Zoom platform. The virtual exercise sessions include 3 parts: cardiovascular exercise, resistance training, and balance or stretching exercise. During sessions, patients will wear provided heart rate monitors with a training goal of moderate intensity, defined as 40-60% of heart rate reserve. Based on the participant's rate of perceived exertion (RPE), heart rate, and individual response during each session, trainers will follow an algorithm designed by the PI and collaborators to progress or regress intensity level. Participant will attend a class on creating and maintaining behavior changes.

Locations

Country	Name	City	State
United States	IU Health West	Avon	Indiana
United States	IU Health Joe and Shelly Schwarz Cancer Center	Carmel	Indiana
United States	Indiana University Melvin & Bren Simon Cancer Center	Indianapolis	Indiana
United States	Sidney and Lois Eskenazi Hospital	Indianapolis	Indiana

Sponsors (1)

Lead Sponsor	Collaborator
Indiana University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in cardiorespiratory fitness	Measured by minutes on the treadmill	baseline, 16 weeks
Secondary	physical performance battery	total score on short physical performance battery	baseline, 8, and 16 weeks
Secondary	Mean quality of life, as measured by the Patient-Reported Outcomes Measurement Information System-29	Likert-scaled questionnaire, with response scores ranging from 1 to 5. Scores alternate from 1 or 5 being the lowest value.	baseline, 8, and 16 weeks
Secondary	muscle mass	measured by mg/kg2 on HU on CT scans	baseline, and 16 weeks
Secondary	muscle density	measured by mg/kg2 on HU on CT scans	baseline, and 16 weeks
Secondary	adipose mass	measured by mg/kg2 on HU on CT scans	baseline, and 16 weeks
Secondary	Change in physical activity minutes	measured by accelerometer data	baseline to post 16-week intervention
Secondary	Change in steps per day	measured by accelerometer data	baseline to post 16-week intervention
Secondary	Mean fatigue score as measured by the basic fatigue inventory (BFI)	Likert-scaled questionnaire, with response scores ranging from 0 to 10, with 10 being the worse response.	baseline, and16-weeks
Secondary	Change intention and habits, as measured by the Behavioral Theory Scales	Likert-scaled questionnaire, measured with a 5-point Likert scale with response options ranging from "strongly disagree" to "strongly agree." Total scores are summed in the range of 40 to 200, with a higher score indicating stronger motivation that could predict exercise behavior.	baseline, and 16-weeks
Secondary	Uptake of the study	the proportion of total patients approached, screened, and ultimately completing the baseline assessments	date open to accrual until closed to accrual, up to 5 years
Secondary	Adherence with the intervention defined	the proportion of scheduled sessions attended by participants randomized to the exercise intervention arm	baseline to post 16-week intervention
Secondary	change in patient-reported functional limitations, as measured by a functional limitations scale	mean score of 5 question scale, where participants responses are either scored 0 or 1, with "some difficulty" a 1 and "no difficulty" as a 0.	baseline, and16-weeks