Clinical Trial Research Participation Agreement

Patient Consent and Documentation Template for Oncology Research Studies

Oncology

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Last updated: Mar 24, 2025

Patient Information

Name: _________________________ Date of Birth: _________________ Medical Record #: ______________

Study Details

Protocol Number: _______________ Principal Investigator: __________ Study Title: ___________________

Participation Agreement

1. Voluntary Participation

I understand that my participation in this oncology research study is entirely voluntary. I may withdraw at any time without affecting my current or future medical care.

2. Study Procedures

I acknowledge that I have been informed about and understand:

  • The purpose of the research study
  • The experimental procedures and treatments involved
  • The duration of my participation
  • The potential risks and benefits
  • Alternative treatment options

3. Confidentiality

I understand that:

  • My medical information will be kept confidential
  • Study data will be coded to protect my identity
  • Access to my records is limited to authorized research personnel

4. Costs and Compensation

  • Study-related procedures: □ Covered □ Not covered
  • Standard care procedures: □ Covered □ Not covered
  • Travel compensation: □ Yes □ No

5. Contact Information

Principal Investigator: _____________ Phone: _________________________ Emergency Contact: ______________

Signatures

Patient Signature: ________________ Date: ________

Investigator Signature: ____________ Date: ________

Witness Signature: _______________ Date: ________

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