Testing Home-based Exercise Strategies in Underserved Minority Cancer Patients Undergoing Chemotherapy: the THRIVE Study
Purpose
The purpose of this research is to determine whether a 16 week, home-based, aerobic and resistance exercise intervention will increase physical activity levels in Black and Hispanic breast, colorectal, or prostate cancer patients. The names of the study interventions involved in this study are: - Supervised aerobic and resistance exercise (SUP) - virtually supervised 16- week aerobic and resistance exercise performed at home via Zoom. - Unsupervised aerobic and resistance exercise (UNSUP) - home-based 16- week aerobic and resistance exercise. - Attention control (AC) - 16-week home-based stretching.
Conditions
- Breast Cancer
- Colorectal Cancer
- Prostate Cancer
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Over 18 years old; children under the age of 18 will be excluded due to rarity of disease - Newly diagnosed with stage I-III breast, colorectal or prostate cancer - Self-identify as Hispanic or Black - Are within 4 weeks of initiating chemotherapy - Overweight or obese (BMI >25kg/m2 or body fat percent >30) - Physician's clearance to participate in moderate-vigorous intensity exercise - Speak English or Spanish - Engaging in less than 90 minutes of moderate-or-vigorous physical activity per week - Willing to travel to Dana-Farber Cancer Institute for necessary data collection - Ability to understand and the willingness to sign a written informed consent document.
Exclusion Criteria
- Pre-existing musculoskeletal or cardiorespiratory conditions - Patients should not have any uncontrolled illness including ongoing or active infection, uncontrolled diabetes, hypertension, or thyroid disease - Patients with other active malignancies - Patients with metastatic disease - Participate in more than 90 minutes of structured exercise/week - Unable to travel to Dana-Farber Cancer Institute for necessary data collection - Subjects, who in the opinion of the investigator, may not be able to comply with the safety monitoring requirements of the study.
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Supportive Care
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Supervised aerobic and resistance exercise (SUP) |
Participants will be randomly assigned to receive 3x weekly at home, virtually supervised aerobic and resistance exercise sessions with a certified exercise trainer for 16 weeks. Participants will also have a baseline test, mid intervention cardiovascular and strength tests and one postintervention and one follow up visit. |
|
|
Experimental Unsupervised aerobic and resistance exercise (UNSUP) |
Participants will be randomly assigned to receive 3x weekly at home, unsupervised aerobic and resistance exercise sessions with a 1x weekly telehealth call with a certified exercise trainer for 16 weeks. Participants will also have a baseline test, mid intervention cardiovascular and strength tests and one postintervention and one follow up visit. |
|
|
Active Comparator Attention Control (AC) |
Participants will be randomly assigned to receive 3x weekly at home stretching exercise for 16 weeks. Participants will also have a baseline test, mid intervention cardiovascular and strength tests and one postintervention and one follow up visit. |
|
Recruiting Locations
Boston, Massachusetts 02115
Christina Dieli-Conwright, PhD, MPH
617-582-8321
ChristinaM_Dieli-Conwright@DFCI.HARVARD.EDU
More Details
- Status
- Recruiting
- Sponsor
- Dana-Farber Cancer Institute
Study Contact
Christina Dieli-Conwright, PhD, MPH617-582-8321
ChristinaM_Dieli-Conwright@dfci.harvard.edu
Detailed Description
This is a randomized control trial of Black and Hispanic patients who have been newly diagnosed with breast, colorectal, or prostate cancer and are being prescribed chemotherapy to determine the effects of home-based exercise on levels of physical activity. It will also evaluate the impact of home-based exercise on cardiovascular (heart health) risk factors. The research study procedures include: screening for eligibility and study treatment including evaluations of body composition, blood tests, fitness and strength assessments, and surveys at study entry and follow-up visits. Participants in this study will be randomly assigned to one of three groups: 1) Supervised aerobic and resistance exercise (SUP), 2) Unsupervised aerobic and resistance exercise (UNSUP), or 3) Attention control (AC). Participation is expected to last for 8 months. It is expected that about 135 people will take part in this research study.