Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06614647

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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.
Not Eligible

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

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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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