Can a digital rehab program help colon cancer patients recover at home?
NCT ID NCT06593678
First seen Jun 27, 2026 · Last updated Aug 12, 2026 · Updated 3 times
Summary
This study tests whether a home-based telerehabilitation program can improve functional capacity and quality of life for patients recovering from colorectal cancer surgery. Fifty-four participants will either follow the digital program or receive a standard booklet. The goal is to see if remote exercise and support can aid recovery without needing frequent hospital visits.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Telerehabilitation program (asynchronous digital platform with exercise videos)
- What this could lead to
- If it works, this could offer a convenient, home-based way to help colorectal cancer patients recover faster and feel better after surgery.
- What could go wrong
- This is a small, early-stage trial with only 54 participants, so results may not apply to everyone. The program depends on patient motivation and access to technology.
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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80 people
The number who actually took part.
- Started
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Aug 2024
- Finished
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Jul 2026
- 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 to 80 years
- 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: * Age between 18 and 80 years. * Participants who understand Spanish. * Patients scheduled for colorectal cancer surgery at Royo Villanova Hospital, Zaragoza, Spain. * Patients attending the first consultation in the General and Digestive Surgery Section under the supervision of Dr. Blas, head of surgery at Royo Villanova Hospital, Zaragoza, Spain. * Participants with functional independence that allows them to perform walking and pulmonary function tests. * Patients with a preoperative assessment score of I, II, or III on the American Society of Anesthesiologists (ASA) scale. * Participants who agree to participate and sign the informed consent form. Exclusion Criteria: * Patients older than 80 years. * Patients with a preoperative ASA score of IV. * Patients with any injury, pathology, or inflammatory processes that make it impossible to practice exercise. * Patients with central and/or peripheral neurological diseases that prevent them from following the rehabilitation program. * Patients with unstable cardiac comorbidities such as arrhythmias, high blood pressure, angina pectoris, or other conditions that contraindicate moderate-intensity training. * Patients diagnosed with a psychiatric disorder as confirmed by a psychiatrist. * Patients without access to mobile internet or a computer with internet at home. * Patients who score ≤ 24 on the Mini-Mental State Examination (MMSE). * Individuals who are unable to follow oral and written instructions in Spanish. * Patients who refuse to participate in the study or who have not signed the informed consent form.
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Genom att skicka in godkänner du våra Användarvillkor
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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Hospital Royo Villanova
Zaragoza, Zaragoza, 50015, Spain
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Other studies related to the condition(s) this trial covers.
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