Actively Recruiting
RESPONSE: Colorectal Cancer Survivors' Follow-up Care - Now Digital and Need-based
Led by University of Aarhus · Updated on 2026-05-04
400
Participants Needed
9
Research Sites
280 weeks
Total Duration
On this page
Sponsors
U
University of Aarhus
Lead Sponsor
A
Aarhus University Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
Over the last decades, the 3-year recurrence rates for patients with stage I and II colorectal cancer have decreased to just 5% and 12%. The follow-up program offered to stage I and low-risk stage II patients has not changed accordingly and is still focused solely on recurrence detection. Moreover, it is a one-size-fits-all program, i.e. most of the follow-up resources are spent on non-recurrence patients who do not benefit. Up to 50% of cancer survivors suffer from reduced quality of life related to fear of cancer recurrence, treatment-related psychological distress, and/or severe late adverse effects of a biopsychosocial and/or organ-specific origin. Today many of these symptoms can be treated effectively. However, no systematic program aimed at monitoring and addressing the symptoms has been implemented yet. The current project is testing a newly developed, digitally managed, patient-centered follow-up program that focuses on individual patient needs, including fear of cancer recurrence, psychological well-being, management of late adverse effects, and recurrence surveillance. This new program will be compared to the current standard of care in a national network of 11 colorectal cancer surgical centers in four of five Danish regions. Patients in the intervention group will receive the following: 1. Risk-stratified circulating tumor DNA (ctDNA) guided recurrence surveillance. 2. Late adverse effects monitoring with electronic patient-reported outcome measures, which are validated questionnaires that can identify and qualify late adverse effects. 3. Systematic treatment for organ-specific and/or biopsychosocial late adverse effects. 4. A digital care guide, to support the patient trajectory through the follow-up program, as a smartphone app. Patients in the standard group will receive standard-of-care follow-up. The primary study endpoint will be the difference in health-related quality of life between the intervention and standard group. Secondary outcomes include e.g., comparison of health-related costs, differences in fear of cancer recurrence, recurrence-free survival, and patient satisfaction. The investigators expect the new follow-up program to be better than the standard-of-care program in terms of the primary endpoint - quality of life - without compromising recurrence detection, and without increasing costs.
CONDITIONS
Official Title
RESPONSE: Colorectal Cancer Survivors' Follow-up Care - Now Digital and Need-based
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients treated for stage I and low risk stage II colorectal cancer with curative intend.
- Age 18 years or older.
- Understands spoken and written Danish language.
- Able to use digital care-guide as smartphone application.
- The patient is also included in DANISH.MRD part 1.
You will not qualify if you...
- Patients unlikely to comply with the protocol or complete the study.
- Patients unable or unwilling to use the digital platform.
- Patients treated only with local endoscopic resection, such as Transanal Endoscopic Microsurgery (TEM).
AI-Screening
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Trial Site Locations
Total: 9 locations
1
Gødstrup Hospital
Herning, Central Jutland, Denmark, 7400
Actively Recruiting
2
Regional Hospital Randers
Randers, Central Jutland, Denmark, 8930
Actively Recruiting
3
Aalborg University Hospital
Aalborg, North Denmark, Denmark, 9000
Actively Recruiting
4
Odense University Hospital
Odense, The Region of Southern Denmark, Denmark, 5000
Actively Recruiting
5
Svendborg Sygehus
Svendborg, The Region of Southern Denmark, Denmark, 5700
Actively Recruiting
6
Aarhus University Hospital
Aarhus, Denmark, 8000
Actively Recruiting
7
Bispebjerg Hospital
Copenhagen, Denmark, 2400
Actively Recruiting
8
Regional Hospital Horsens
Horsens, Denmark, 8700
Actively Recruiting
9
Regional Hospital Viborg
Viborg, Denmark, 8800
Actively Recruiting
Research Team
C
Claus L Andersen, Prof.
CONTACT
M
Mai-Britt W Ørntoft, Ass. Prof.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
DIAGNOSTIC
Number of Arms
2
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