Weight Loss Programs for Kidney Cancer Prevention

This study is comparing two different weight loss programs, Intermittent Fasting (IF) and Continuous Energy Restriction (CER), for people with small kidney (renal) cancer masses who are under active surveillance (AS). The goal is to see if these programs can help prevent the cancer from getting worse. You could be eligible if you are an English-speaking adult (18+) with a biopsy-confirmed kidney cancer mass, are on active surveillance for less than 5 years, and have a BMI of 25 or higher. The study aims to see how many people participate in each program over 6 months. This study is currently recruiting about 20 participants.

Study design
This interventional study compares two different weight loss programs, Intermittent Fasting and Continuous Energy Restriction, with about 20 participants.
What's involved
You would participate in either the Intermittent Fasting or Continuous Energy Restriction program, which includes self-monitoring and feedback from an interventionist.
Compensation
Not stated in the trial record.
Follow-up
The primary endpoint, participation rate, is measured at 6 months.

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

NCT07714018

Comparing Two Weight Loss Programs for the Prevention of Kidney Cancer Progression Among Patients With Small Renal Masses on Active Surveillance

Not Yet Recruiting
NAAges 18+InterventionalPrevention
Roswell Park Cancer Institute
~20 participants
Updated 2026-07-20 on ClinicalTrials.gov
What's tested:Intermittent FastingContinuous Energy Restriction (CER)

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Participation Rate
Measured over At 6 months
Renal Cell Carcinoma (RCC)
1 sites across 1 states
New York1

This trial hasn't published a contact. View it on ClinicalTrials.gov

Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

English speaking
SRM patient with biopsy-confirmed RCC who are initiating or already on AS for less than 5 years
Age 18 years or older
Body mass index (BMI) ≥ 25 kg/m\^2
No medical problems that might contraindicate participation in a behavioral weight reduction program containing an exercise component
No current medication that might affect weight loss
Not pregnant or lactating
No more than 5% body weight loss in the past 3 months
No bariatric surgery in the last 10 years

Exclusion

Non-English speaking
Less than 18 years old
BMI \< 25 kg/m\^2
Medical problems that might contraindicate participation in a behavioral weight reduction program containing an exercise component
Current medication that might affect weight loss
Pregnant or lactating
More than 105% body weight loss in the past 6 months
Bariatric surgery in the last 10 years
Medical conditions that might contraindicate short-term fasting periods
Unwilling or unable to follow protocol requirements
Received an investigational agent within 30 days prior to enrollment
  • Participation RateAt 6 months

    This will assess the rate of eligible persons who enroll after invitation and the mean proportion of intervention components completed by arm and participant