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.
Precise Oncology Interventions in Nutrition and Training (OnPoint)
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Tracy Crane, PhD, RDN · PRINCIPAL_INVESTIGATOR · University of Miami
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- 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.