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Precise Oncology Interventions in Nutrition and Training (OnPoint)
NCT06534918 · University of Miami
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
About this study
The purpose of this study is to see if survivors of breast, prostate, or colorectal cancer who receive a personal referral to a targeted nutrition and exercise program will be able to eat a healthier diet and be more physically activity.
Eligibility criteria
Inclusion Criteria:
Inclusion Criteria - Healthcare Providers
1. Provide full- or part-time care in an oncology clinical care setting at Sylvester Comprehensive Cancer Center
2. Utilize the electronic medical record for patient documentation on a regular basis
3. Willing to complete a 30-60-minute interview
Inclusion Criteria - Patients
1. 18 years of age or older
2. Any sex/gender
3. Able to provide consent
4. Able to read/understand English or Spanish
5. Diagnosis of breast, prostate or colorectal cancer, 6 months post completion of primary treatment, with no evidence of primary disease
6. Approval from treating oncologist, confirmed via email or in writing
7. Fail to meet at least one of the American Cancer Society guidelines: engaging in \>150 minutes of moderate-to-vigorous physical activity per week for the prior month or consuming at least 3 cups of vegetables and 2 cups of fruit per day over the past month.
8. Internet access on a smart phone, tablet, or computer
9. Agree to be randomly assigned to any study group
Exclusion Criteria:
1. Less than 18 years of age
2. Unable to provide consent
3. Unable to read/understand English or Spanish
4. Any contraindication for diet change or exercising as determined by physician
5. Blank
6. Engaging in \>150 minutes of moderate to vigorous physical activity on average per week for the prior month
7. Meeting the American Cancer Society diet recommendations (3 cups of vegetables or legumes, 2 cups of fruit, 2 serving whole grain per day, and limited red/processed meats, sugar-sweetened beverages, and highly processed foods) for the prior month
8. History of dementia or major psychiatric disease which would interfere with study participation
9. History of recent (≤1 yr) stroke, myocardial infarction or congestive heart failure
10. Eastern Cooperative Oncology Group (ECOG) score of \>2
11. Severe lymphedema as determined by physician
12. Receiving physical therapy treatment
Study design
Enrollment target: 306 participants
Allocation: randomized
Masking: single
Age groups: adult, older_adult
Timeline
Starts: 2024-09-18
Estimated completion: 2027-09-30
Last updated: 2025-09-19
Interventions
Other: FitbitBehavioral: Nutrition Course: Group SessionsBehavioral: Physical Activity Program: Group SessionsBehavioral: Nutrition Course: One on One Sessions with Registered DietitianBehavioral: Physical Activity Program: One on One Sessions with an Exercise PhysiologistBehavioral: Nutrition and Physical Activity Prescription
Primary outcomes
- • Percentage of Survivors Who Agree to Participate (Up to 8 Weeks)
- • Percentage of Interventions Sessions Completed (Up to 8 Weeks)
- • Percentage of Participants Satisfied with the Intervention (Up to 8 Weeks)
Sponsor
University of Miami · other
With: The Applebaum Foundation
Contacts & investigators
ContactGrey Freylersythe, BS · contact · g.freylersythe@med.miami.edu · 305-243-9832
ContactTracy Crane, PhD, RDN · contact · tecrane@med.miami.edu · 305-243-8255
InvestigatorTracy Crane, PhD, RDN · principal_investigator, University of Miami
All locations (1)
University of MiamiRecruiting
Miami, Florida, United States