Can a 10-Week lifestyle program boost fitness after cancer?
NCT ID NCT04987359
First seen Sep 17, 2026 · Last updated Sep 18, 2026 · Updated 1 time
Summary
Researchers test a 10-week lifestyle program for people who have finished cancer treatment. The program combines structured exercise, nutrition counseling, and behavioral therapy. They compare it with a waitlist group to see how it affects cardiorespiratory fitness and body weight. Participants must have a history of cancer and a body mass index of 30 or higher, or 27 or higher with related health conditions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a 10-week program combining structured exercise training, nutritional counseling, and intensive behavioral therapy
- What this could lead to
- If it works, this could give cancer survivors a structured way to improve fitness and manage weight after treatment.
- What could go wrong
- The trial is small, with 33 participants, and a 10-week program may not produce lasting changes. Fitness and weight can be hard to shift, and results might not apply to all survivors.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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33 people
The number who actually took part.
- Started
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Aug 2021
- Finished
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Feb 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Ability to provide informed consent before any trial-related activities * History of any malignancy * Completion of cancer-directed therapy (e.g., surgery, chemotherapy, and radiotherapy) prior to enrollment (patients receiving ongoing endocrine or targeted therapy are eligible to participate) * No evidence of residual or recurrent cancer under active treatment * Age ≥18 years * Body mass index (BMI) ≥30 kg/m2 or BMI ≥27 kg/m2 with one or more treated or untreated weight-related coexisting conditions * Willing to be randomized * Allow the collection and storage of biospecimens and data for future use Exclusion Criteria: * Engaging in ≥3 purposeful exercise sessions per week, on average, over the past 12 weeks * Significant purposeful weight loss (\>11 kg) within the past 12 weeks * Current use of medications or devices for the purpose of weight loss * Metabolic or bariatric surgery within the last year * Cardiovascular, respiratory, or musculoskeletal disease that would prohibit participation in an exercise and weight loss program * Currently pregnant, breastfeeding, or planning to become pregnant with the next 12 weeks * Psychiatric disorders or conditions that would preclude participation in the study intervention * Any other condition which, in the opinion of the investigator, may impede testing of the study hypothesis or make it unsafe to engage in the study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Pennington Biomedical Research Center
Baton Rouge, Louisiana, 70808, United States
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