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Recruiting NCT07427901

Quality Of Life In Colorectal Cancer Survivors

No phase Interventional Colorectal Cancer Colon Cancer Rectal Cancer

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Quality of Life Assessment.
Who it may be relevant to
Registry conditions: Colorectal Cancer, Colon Cancer, Rectal Cancer. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Slovenia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The purpose of this study is to identify late adverse effects in colorectal cancer patients that may influence quality of life at 6, 12, and 24 months after oncological treatment. The study aims to assess quality of life in colorectal cancer survivors in relation to psycho-physical-social well-being at different time points and to evaluate the prevalence of late adverse effects and their association with diagnosis and specific oncological treatment.

Detailed description

The purpose of this study is to identify late adverse effects in patients with colorectal cancer that may influence quality of life at 6, 12, and 24 months after oncological treatment. The study will assess quality of life in colorectal cancer patients in relation to psycho-physical-social well-being at different time points. In addition, the study will identify and evaluate the prevalence of late adverse effects and analyze their association with diagnosis and specific oncological treatment.

Interventions

  • Other Quality of Life Assessment
    Quality of life assessment using questionnaires at 6, 12, and 24 months after oncological treatment.

Primary outcome measures

  • Quality of Life Score (EORTC QLQ-C30 Global Health Status/QoL Scale) [Time frame: 6, 12, and 24 months after oncological treatment]
Secondary outcome measures (1)
  • Colorectal Cancer-Specific Quality of Life (EORTC QLQ-CR29) [Time frame: 6, 12, and 24 months after oncological treatment]

Eligibility criteria

Inclusion criteria

  • Patients with colorectal cancer (colon or rectal cancer)
  • Age 25 to 65 years
  • First oncological treatment performed at the Institute of Oncology Ljubljana
  • Working-capable patients
  • Ability to complete questionnaires
  • Ability to provide written informed consent

Exclusion criteria

  • Age < 25 years or > 65 years
  • Patients unable to complete questionnaires
  • Patients unable to participate in follow-up assessments
  • Patients who do not provide written informed consent

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Other

Study locations

Slovenia · 1 center
  • Institute of Oncology Ljubljana — Ljubljana

Identifiers

NCT: NCT07427901 · OIL_CCS_2023 · ERIDNPVO-0051/2023 · 0120-192/2023/6

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗