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QoLiCOL - Quality of Life in Colon Cancer

S

Sahlgrenska University Hospital

Status

Active, not recruiting

Conditions

Colonic Neoplasm

Treatments

Behavioral: There is no intervention, only observation

Study type

Observational

Funder types

Other

Identifiers

NCT02530593
QoLiCOL

Details and patient eligibility

About

All patients presenting at participating hospitals during the recruitment period with a newly diagnosed colon cancer, regardless of stage and planned treatment, will be eligible for inclusion. They will answer a questionnaire on health related quality of life, physical symptoms, functional impairments and socioeconomic status at diagnosis and after 12, 36 months. Clinical data including recurrence, survival, surgical treatment, oncologic result (pathology report) and adjuvant treatment will be collected from the Swedish ColoRectal Cancer Registry (SCRCR)

Full description

QoLiCOL is an explorative, prospective, longitudinal, non-interventional, international, multicenter study of health-related quality of life, physical symptoms, functional impairments and socioeconomic burden in colon cancer patients. All patients presenting at participating hospitals during the recruitment period with a newly diagnosed rectal cancer, regardless of stage and planned treatment, will be eligible for inclusion. Patients will be followed for 3 years. They will be asked to answer questionnaires at three different time points during follow-up: at diagnosis and after 12 and 36 months. Clinical data, including recurrence, surgical treatment, oncologic result (pathology report) and adjuvant treatment will be collected from the national quality registry for rectal cancer in Denmark and Sweden. As these registries differ in some areas between the countries, additional data will be collected through short CRF:s.

Enrollment

1,500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Colon cancer newly diagnosed.
  • Planned treatment presented

Exclusion criteria

  • No Colon cancer diagnosis,
  • below 18 years of age,
  • no informed consent or withdrawn informed consent.

Trial design

1,500 participants in 1 patient group

Patients with colon cancer
Description:
All patients presenting with a newly diagnosed colon cancer regardless of tumour stage
Treatment:
Behavioral: There is no intervention, only observation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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