Precise Oncology Interventions in Nutrition and Training (OnPoint)

Status: Recruiting
Location: See location...
Intervention Type: Other, Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Provide full- or part-time care in an oncology clinical care setting at Sylvester Comprehensive Cancer Center

• Utilize the electronic medical record for patient documentation on a regular basis

• Willing to complete a 30-60-minute interview

• 18 years of age or older

• Any sex/gender

• Able to provide consent

• Able to read/understand English or Spanish

• Diagnosis of breast, prostate or colorectal cancer, 6 months post completion of primary treatment, with no evidence of primary disease

• Approval from treating oncologist, confirmed via email or in writing

• 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.

• Internet access on a smart phone, tablet, or computer

• Agree to be randomly assigned to any study group

Locations
United States
Florida
University of Miami
RECRUITING
Miami
Contact Information
Primary
Grey Freylersythe, BS
g.freylersythe@med.miami.edu
305-243-9832
Backup
Tracy Crane, PhD, RDN
tecrane@med.miami.edu
305-243-8255
Time Frame
Start Date: 2024-09-18
Estimated Completion Date: 2027-09-30
Participants
Target number of participants: 306
Treatments
Experimental: Low Complexity Group
Participants in this group will receive the low complexity intervention for up to eight (8) weeks.
Experimental: Moderate Complexity Group
Participants in this group will receive the moderate complexity intervention for up to eight (8) weeks.
Experimental: High Complexity Group
Participants in this group will receive the high complexity intervention for up to eight (8) weeks.
No_intervention: Control Group
Participants randomized to this arm will receive routine care and will not receive any study materials until the end of the study at 24 weeks.
Sponsors
Collaborators: The Applebaum Foundation
Leads: University of Miami

This content was sourced from clinicaltrials.gov