Physical Activity Intervention to Reduce Functional Health Disparities Among Breast Cancer Survivors

NCT02763228 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 218

Last updated 2022-03-22

No results posted yet for this study

Summary

The purpose of this research study is to determine whether a physical activity (exercise) program in the community will improve the functional and overall health status of older women with a history of breast cancer. The physical activity or exercise program is designed for all older breast cancer survivors, and in particular for African-Americans and women of lower socio-economic status, who are the least likely to engage in physical activity.

Conditions

Interventions

BEHAVIORAL

Aerobic Training - Fixed Schedule

Supervised aerobic training for 40 minutes 3x/week for 20 weeks

BEHAVIORAL

Resistance Training - Fixed Schedule

Supervised resistance training for 20 minutes 3x/week for 20 weeks

BEHAVIORAL

Walking program

Unsupervised walking program 1-3 days/week for 52 weeks

BEHAVIORAL

Aerobic Training - Flexible Schedule

Supervised aerobic training done on the participant's own schedule for 32 weeks

BEHAVIORAL

Resistance Training - Flexible Schedule

Supervised resistance training done on the participant's own schedule for 32 weeks

BEHAVIORAL

Successful Survivorship Health Education and Support Group

Support groups will be held for one hour 3x/week for 20 weeks. Topics will include, but are not limited, to long-term side effects of treatment, stress management, coping with fear and uncertainty, body image, sexuality, and spirituality.

BEHAVIORAL

Flexible support groups

Participants will attend 1-3 weekly group sessions of their choosing for 32 weeks.

Sponsors & Collaborators

  • National Institutes of Health (NIH)

    collaborator NIH
  • Case Comprehensive Cancer Center

    lead OTHER

Principal Investigators

  • Cynthia Owusu, MD · University Hospitals Cleveland Medical Center, Case Comprehensive Cancer Center

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
65 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-03-16
Primary Completion
2020-03-25
Completion
2020-11-06

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02763228 on ClinicalTrials.gov