Exercise and Diet Counseling Program in Improving Quality of Life in Stage I-III Breast Cancer Survivors

  • STATUS
    Recruiting
  • participants needed
    20
  • sponsor
    Ohio State University Comprehensive Cancer Center
Updated on 16 February 2024
cancer
body mass index
breast cancer
hormone therapy
endocrine therapy
nutrition education
active treatment
aerobic exercise
resistance training
female breast cancer
stage iii breast cancer
nutritional assessment
stage iiib breast cancer
stage ii breast cancer
stage i breast cancer
stage iiia breast cancer
anatomic stage iia breast cancer ajcc v8
anatomic stage iib breast cancer ajcc v8
anatomic stage iiia breast cancer ajcc v8
prognostic stage iia breast cancer ajcc v8
prognostic stage iib breast cancer ajcc v8
prognostic stage iiib breast cancer ajcc v8
prognostic stage iii breast cancer ajcc v8
prognostic stage ii breast cancer ajcc v8
stage iiic breast cancer
prognostic stage ia breast cancer ajcc v8
anatomic stage ia breast cancer ajcc v8
prognostic stage iiic breast cancer ajcc v8
anatomic stage iii breast cancer ajcc v8
prognostic stage iiia breast cancer ajcc v8
prognostic stage ib breast cancer ajcc v8
anatomic stage i breast cancer ajcc v8
stage iib breast cancer
anatomic stage ii breast cancer ajcc v8
anatomic stage ib breast cancer ajcc v8
stage ia breast cancer
stage ib breast cancer
stage iia breast cancer
anatomic stage iiib breast cancer ajcc v8
anatomic stage iiic breast cancer ajcc v8
prognostic stage i breast cancer ajcc v8

Summary

This trial studies the benefits of an exercise and diet counseling program in improving quality of life in stage I-III breast cancer survivors. Exercise and diet counseling may help improve weight loss and relevant clinical and patient-reported outcomes in overweight or obese breast cancer survivors.

Description

PRIMARY OBJECTIVES:

I. To determine the feasibility of delivering a community-based, comprehensive lifestyle weight management (LWM) intervention to 20 overweight or obese breast cancer (BC) survivors.

II. Explore preliminary efficacy of the community-based, comprehensive LWM intervention for producing meaningful improvements in select clinically-relevant anthropometric, fitness, functional, and patient-reported outcomes in BC survivors.

III. Provide the effect size estimates necessary to inform the design of a subsequent R01 application addressing a large scale, optimally powered, randomized controlled, community-based LWM comparative efficacy intervention trial targeting weight loss in BC survivors.

OUTLINE

Patients undergo aerobic exercise over 10-30 minutes and resistance exercise comprising 1-3 sets of 8-12 repetitions of 10 different exercises over 1 hour for 24 weeks. Patients also receive behavioral activity counseling once a week and nutritional counseling over 30 minutes for 10 sessions after center-based exercise sessions during months 1-2.

After completion of study, patients are followed up at 3 and 6 months.

Details
Condition Overweight, Obesity, Obesity, Anatomic Stage I Breast Cancer AJCC v8, Anatomic Stage IA Breast Cancer AJCC v8, Anatomic Stage IB Breast Cancer AJCC v8, Anatomic Stage II Breast Cancer AJCC v8, Anatomic Stage IIA Breast Cancer AJCC v8, Anatomic Stage IIB Breast Cancer AJCC v8, Anatomic Stage III Breast Cancer AJCC v8, Anatomic Stage IIIA Breast Cancer AJCC v8, Anatomic Stage IIIB Breast Cancer AJCC v8, Anatomic Stage IIIC Breast Cancer AJCC v8, Prognostic Stage I Breast Cancer AJCC v8, Prognostic Stage IA Breast Cancer AJCC v8, Prognostic Stage IB Breast Cancer AJCC v8, Prognostic Stage II Breast Cancer AJCC v8, Prognostic Stage IIA Breast Cancer AJCC v8, Prognostic Stage IIB Breast Cancer AJCC v8, Prognostic Stage III Breast Cancer AJCC v8, Prognostic Stage IIIA Breast Cancer AJCC v8, Prognostic Stage IIIB Breast Cancer AJCC v8, Prognostic Stage IIIC Breast Cancer AJCC v8, Cancer Survivor
Age 30years - 75years
Treatment aerobic exercise, resistance training, Nutritional Assessment, Questionnaire Administration, Quality-of-Life Assessment, Exercise Counseling
Clinical Study IdentifierNCT04454086
SponsorOhio State University Comprehensive Cancer Center
Last Modified on16 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Female breast cancer (stage I-III), within (w/in) 60 months after cessation of active treatment (surgery, chemotherapy, radiation), and may be on continued hormone therapy
Overweight/obese (body mass index [BMI] > 25)
Ability to understand and the willingness to sign a written informed consent
Willing and physically able to participate in physical activity
Obtain physician consent via primary care physician and/or treating oncologist

Exclusion Criteria

> 60 months post breast cancer therapy
Contraindications to exercise
Diagnosis of cancer other than breast that is receiving active treatment
Currently receiving chemotherapy/radiation
Musculoskeletal/neurological disorder inhibiting them from safe exercise
Pregnant or nursing women
Unable to give informed consent
Clear my responses

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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