Exercise and diet may ease nerve damage and fatigue during chemo
NCT ID NCT03885817
First seen Jul 20, 2026 · Last updated Jul 21, 2026 · Updated 1 time
Summary
This study tests whether a tailored exercise program and nutritional guidance can reduce peripheral neuropathy (nerve damage) and fatigue in people with colorectal cancer receiving chemotherapy. Participants follow a supervised exercise routine and monthly nutrition check-ins during their treatment. The goal is to improve quality of life by managing common side effects of chemotherapy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- an exercise program and nutritional guidance
- What this could lead to
- If it works, this could offer a simple, drug-free way to ease nerve pain and tiredness during chemotherapy.
- What could go wrong
- This is a small, early-stage trial, so results may not apply to everyone. The benefits may be modest or hard to separate from standard care.
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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66 people
The number who actually took part.
- Started
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Mar 2019
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Radical resection for colon- or rectal cancer past 3 months, and scheduled for adjuvant, Oxaliplatin-based, combination chemotherapy. * Histologically confirmed adenocarcinoma. * Able to read and understand Norwegian. * Able to carry out the intervention. * Performance Status (PS) 0 - 2. Exclusion Criteria: * Serious comorbidities that contraindicate physical exercise, based on the treating physician's assessment. * Unable to give informed consent. * Treated for other cancer last 5 years prior to inclusion (with the exceptions of basal cell carcinoma of the skin and carcinoma in situ in the cervix). * Prior treatment with Oxaliplatin
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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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Kreftklinikken, St Olavs Hospital
Trondheim, Norway
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Levanger sykehus
Levanger, Norway
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Sørlandet sykehus, Kristiansand
Kristiansand, Norway
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Ullevål
Oslo, Norway
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Ålesund sjukehus
Ålesund, Norway
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