Interventional study to optimize the preventive behavior in first-degree relatives of patients with colorectal carcinoma

Not Applicable

• Conditions: Colorectal carcinoma (CRC) prevention, the preventive behavior in first-degree relatives; C26.0; Intestinal tract, part unspecified

• Registration Number: DRKS00006818
• Lead Sponsor: Medizinische Klinik II,Onkologie / Hämatologie und Sektion Pneumologie,Hubertus Wald Tumorzentrum,Universitäres Cancer Center (UCCH),Universitätsklinikum Eppendorf

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2014-11-10
• Study Completion: 2016-10-26
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 215

Inclusion Criteria

Patients are diagnosed with colorectal cancer who have relatives
- Existence of the consent of personal data
- Diagnosis max 6 months

1)Histologically confirmed CRC
2)Patients must be 18 years of age.
3)Patients must be able to understand the investigational nature of this study and give written informed consent prior to study entry.

Exclusion Criteria

severe mental illness

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Participation rate of preventive colonoscopy of first-degree relatives six months after intervention; economic efficiency of the training measure of affected patients to improve the preventive behavior of the risk group.