Can exercising at home match gym sessions for cancer recovery?
NCT ID NCT07159815
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study compares a 12-week digital home-based resistance exercise program to a supervised on-site program for cancer survivors who finished treatment up to 5 years ago. The main goal is to see which approach leads to better exercise adherence. Researchers will also measure effects on physical function, mental health, and metabolism. The trial includes 160 participants living near exercise locations in Norway.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- resistance exercise
- What this could lead to
- If successful, this could show that digital home-based exercise is as effective as supervised sessions, making rehabilitation more accessible for cancer survivors.
- What could go wrong
- This is a relatively small, early-stage trial focused on adherence, not direct disease outcomes. Results may not apply to all cancer types or stages.
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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About 160 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2023
- Expected to finish
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Jun 2028
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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Accepted
You do not need to have the condition being studied to take part.
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: * ≥ 18 years and able to give informed consent * Previously diagnosed with any form of cancer and having completed systemic chemotherapy, immunotherapy or targeted therapies or local radiotherapy not more than 5 years earlier * Living within 20 km of one of the exercise locations (Lillehammer, Gjøvik, or Hamar) * Life expectancy of more than 12 months * Access to digital equipment at home (e.g. PC and/or tablet) and an email address, enabling participation on the digital exercise platform * Able to understand the Norwegian language Exclusion Criteria: * Co-morbidities prohibiting exercise according to the protocol, such as serious cardiac, pulmonary, or other organ diseases * Conditions caused by the cancer that prohibits exercise, such as recent major surgery, fractures, or pain * Still undergoing active cancer treatment * Life expectancy of less than 12 months * Reduced mental capacity such that the participant is unable to give informed consent and follow the program * Has performed regular strength training (two or more times per week) within the last three months Note on reference groups: In addition to the randomized controlled trial, the study includes two non-randomized reference groups that are allocated to the digital home-based intervention only and undergo the same test protocol as the randomized participants. These are: (i) patients undergoing active cancer treatment, and (ii) patients who have completed treatment but live more than 20 km from an exercise location. Reference-group participants must otherwise meet the same inclusion criteria regarding age, cancer diagnosis, life expectancy, digital access, and language, and are subject to the same exclusion criteria, except that ongoing active treatment and distance from an exercise location are permitted as defining features of the respective groups. Patients undergoing active cancer treatment that is expected to confer a high risk of bone marrow suppression - leading to infections, bleeding, and/or severely reduced physical capacity - are excluded.
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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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Aktivklinikken
Lillehammer, Norway
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Inland Norway University of Applied Sciences
Lillehammer, Norway
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Innlandet Hospital Trust/ Pusterommet Gjøvik
Gjøvik, Norway
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The Hamar Training Centre
Hamar, Norway
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