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Feasibility of High Levels of Energy Expenditure From Physical Activity for Breast Cancer Survivors

Feasibility of High Levels of Energy Expenditure From Physical Activity During a Weight Loss Intervention for Breast Cancer Survivors

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02963740
Enrollment
11
Registered
2016-11-15
Start date
2016-11-30
Completion date
2017-03-31
Last updated
2022-01-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer Female

Keywords

breast cancer survivor, weight loss program

Brief summary

The purpose of the study is to demonstrate that breast cancer survivors who need to lose weight are able to follow a weight loss program which combines modest calorie restriction with a graduated activity program..

Detailed description

Feasibility will be assessed by 1) the number of women that complete the 3--month program; 2) the number of women that can achieve the targeted amount of physical activity per week by the end of the program; and 3) the median amount of physical activity achieved group by all subjects that complete the program.

Interventions

BEHAVIORALSupervised Exercise

Participants will take part in supervised exercise activities two times per week at a YMCA. Length of the activity will be increased during participation in study. Participants will start at 40 minutes per week and work their way up to 120 minutes per week.

BEHAVIORALHome-based Exercise

Aerobic exercise activities to be completed at home. Participants will be asked to start out doing 60 minutes at home and work up to 180 minutes of purposeful aerobic home exercise per week.

Once weekly phone calls that are group-based. The calls will discuss lifestyle changes specific to participants and cover the effects of diet, physical activity, and weight on breast cancer risk, as well as body image and emotional eating.

BEHAVIORALDiet

Participants will consume a nutritionally balanced, reduced calorie diet as recommended by the Academy of Nutrition and Dietetics.

Sponsors

University of Kansas Medical Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
No minimum to 71 Years
Healthy volunteers
No

Inclusion criteria

* Women \< age 71 in good general health. * Prior diagnosis of breast cancer. * At least 3 months from completion of any cytotoxic chemotherapy or radiation or surgery. May continue to take endocrine therapy and/or maintenance trastuzumab. * Body Mass Index (BMI) 30-45 kg/m2. * By self-assessment, currently performing 60 minutes or less of purposeful exercise per week but able to walk at least 30 minutes on a level surface. * Access to a smart phone capable of running MyFitnessPal and Garmin Connect apps and willing to have diet and exercise data from these apps viewed by study personnel. * Live in the greater Kansas City Metropolitan Area * Willing and able to perform moderate intensity exercise at least 5 days per week for 3 months. * Willing to perform unsupervised home exercise for the entire 3 months. * Willing to participate in a weekly behavioral modification group phone call for 3 months. * Willing to participate in a controlled dietary intervention with portion controlled meals and partial meal and track food intake and exercise.

Exclusion criteria

* Use of metformin, insulin, steroids or weight loss or anti-psychotic drugs within the prior 3 weeks * Individuals with prior bariatric surgery procedures * Need for chronic immunosuppressive drugs * Participation within the past 6 months on a structured weight loss program such as Weight Watchers® * Physical impairments (bad hip, knees, feet, peripheral neuropathy) that would prohibit performing moderate intensity exercise at least 5 days per week. * Any other condition or intercurrent illness that in the opinion of the investigator makes the subject a poor candidate for participation in the trial such as recent cardiac event. * Currently receiving investigational agents in a clinical trial.

Design outcomes

Primary

MeasureTime frameDescription
Adherence to supervised exercise sessionsWeek 12Adherence is defined as the percent of monitored sessions at the YMCA attended by the participant.

Secondary

MeasureTime frameDescription
Percent participants meeting physical activity goalWeek 9 to Week 12Measured as percentage of participants meeting final physical activity goal between week 9 to week 12. Measurement based off activity tracker participants will wear.
Compliance with group telephone sessionsWeek 12Defined as number of participants attending at least 75% of the weekly group calls.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026