Consent Studie.

• Conditions: opt-out; residual tissue; patient information; DNA; informed consent; biobank; cancer; researchgeenbezwaar; restmateriaal; patiëntinformatie

• Registration Number: NL-OMON29536
• Lead Sponsor: KWF Kankerbestrijding

Brief Summary

/A

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 1800

Inclusion Criteria

Patients between the ages of 18 and 80 years whose tissue has been removed.

Exclusion Criteria

Unability to speak and read Dutch. Unability to complete the questionnaires.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. Patients’ satisfaction with and preference for a consent procedure;<br /><br>2. Proportion of patients aware of storage of tissue and research use;<br /><br>3. Consent rates;<br /><br>4. Medical staff’s satisfaction with and preference for a consent procedure.