OnPoint Study: Nutrition and Exercise for Cancer Survivors

This study, called OnPoint, is looking at whether survivors of breast, prostate, or colorectal cancer can improve their diet and physical activity through a personalized nutrition and exercise program. You would receive a Fitbit to track your activity, and participate in nutrition courses (group or one-on-one with a dietitian) and physical activity programs (group or one-on-one with an exercise physiologist). The study aims to see how many survivors join, how many sessions they complete, and how satisfied they are with the program over eight weeks. This study is for adults aged 18 and older who have survived these cancers.

Study design
This is an interventional study with a planned enrollment of 306 participants. It is not specified if it is randomized or blinded.
What's involved
You would wear a Fitbit daily for up to eight weeks. You would also participate in nutrition and physical activity sessions, which could be group classes or weekly one-on-one sessions lasting 30-60 minutes.
Compensation
Not stated in the trial record.
Follow-up
Your participation and satisfaction with the intervention will be measured for up to 8 weeks.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06534918

Precise Oncology Interventions in Nutrition and Training (OnPoint)

Recruiting
NAAges 18+InterventionalSupportive care
University of Miami
~306 participants
Updated 2025-09-19 on ClinicalTrials.gov
What's tested:FitbitNutrition Course: Group SessionsPhysical Activity Program: Group SessionsNutrition Course: One on One Sessions with Registered DietitianPhysical Activity Program: One on One Sessions with an Exercise PhysiologistNutrition and Physical Activity Prescription

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Percentage of Survivors Who Agree to Participate
Measured over Up to 8 Weeks
+2 more outcomes measured
Breast Cancer
Prostate Cancer
Colorectal Cancer
1 sites across 1 states
Florida1
  • Tracy Crane, PhD, RDN · PRINCIPAL_INVESTIGATOR · University of Miami

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  • Percentage of Survivors Who Agree to ParticipateUp to 8 Weeks

    Percentage of survivors who agree to participate will be reported as ≥ 50%.

  • Percentage of Interventions Sessions CompletedUp to 8 Weeks

    Percentage of intervention sessions completed will be reported as ≥ 80%.

  • Percentage of Participants Satisfied with the InterventionUp to 8 Weeks

    Report of 80% satisfaction will be determined as satisfaction with intervention components.