Clinical trial · Interventional
Precise Oncology Interventions in Nutrition and Training (OnPoint)
NCT06534918CI-TRIAL-00095469OnPointrecruitingN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 26, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260926-000001
Summary
Brief summary (as posted)
The purpose of this study is to see if survivors of breast, prostate, colorectal or lymphoma 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.
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Colorectal Cancer | Malignant Colorectal Neoplasm | CURATED_BROADER | 0.80 |
| Lymphoma | Lymphoma | ONTOLOGY_EXACT | 0.90 |
| Prostate Cancer | Malignant Prostate Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (6)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Fitbit | Other | — | UNRESOLVED |
| Nutrition and Physical Activity Prescription | Behavioral | — | UNRESOLVED |
| Nutrition Course: Group Sessions | Behavioral | — | UNRESOLVED |
| Nutrition Course: One on One Sessions with Registered Dietitian | Behavioral | — | UNRESOLVED |
| Physical Activity Program: Group Sessions | Behavioral | — | UNRESOLVED |
| Physical Activity Program: One on One Sessions with an Exercise Physiologist | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (4)
- type
- EXPERIMENTAL
- label
- Low Complexity Group
- description
- Participants in this group will receive the low complexity intervention for up to eight (8) weeks.
- interventionNames
- Other: Fitbit
- Behavioral: Nutrition and Physical Activity Prescription
- type
- EXPERIMENTAL
- label
- Moderate Complexity Group
- description
- Participants in this group will receive the moderate complexity intervention for up to eight (8) weeks.
- interventionNames
- Other: Fitbit
- Behavioral: Nutrition Course: Group Sessions
- Behavioral: Physical Activity Program: Group Sessions
- Behavioral: Nutrition and Physical Activity Prescription
- type
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
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, colorectal or lymphoma 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
References
Publications (0)
Data not yet available
No reference posted for this study.