New rehab program aims to ease life after colorectal cancer
NCT ID NCT07428239
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a personalized rehabilitation program for 150 adults who finished treatment for colorectal cancer. The program connects patients with specialists like physiotherapists, dietitians, and psychologists based on their individual needs. The goal was to improve quality of life and manage long-term physical and emotional effects. No drugs or devices were used.
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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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150 people
The number who actually took part.
- Started
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Oct 2022
- Finished
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Sep 2024
- 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: Adult patients (≥18 years) with histologically confirmed colorectal cancer Patients who have completed primary oncological treatment (surgery ± systemic therapy and/or radiotherapy) Patients eligible for and willing to participate in an individualized comprehensive rehabilitation program Ability to understand the study procedures and provide written informed consent Exclusion Criteria: Severe cognitive impairment or psychiatric condition preventing participation Uncontrolled comorbidities that contraindicate participation in rehabilitation (e.g. severe cardiovascular instability) Inability to participate in follow-up assessments Concurrent participation in another interventional clinical study that could interfere with study outcomes
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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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Institute of Oncology Ljubljana
Ljubljana, 1000, Slovenia
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Other studies related to the condition(s) this trial covers.
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