The Model Consent Form Template UK is offered in multiple formats, including PDF, Word, and Google Docs, featuring both editable and printable versions for your convenience.
Model Consent Form Template UK Editable – PrintableSample
Model Consent Form Template UK 1. Participant Information 2. Researcher Information 3. Research Purpose 4. Description of the Study 5. Risks and Benefits 6. Confidentiality 7. Voluntary Participation 8. Contact Information 9. Consent Statement 10. Signatures
PDF
WORD
Examples
[Name of the Participant]
[Participant’s ID or Reference Number]
[Participant’s Address]
[Participant’s Phone]
[Participant’s Email]
This form is intended to seek consent from the Participant for [describe the specific purpose, e.g., participating in a clinical trial, using personal data for research, etc.].
The Participant has been informed of the following details regarding their involvement: [Provide details about the study or project, including duration, procedures, risks, and benefits].
All personal information collected during this process will be treated confidentially and in compliance with GDPR regulations. The data will be used solely for the purposes stated above.
The Participant has the right to withdraw their consent at any time without any adverse consequences. Such a withdrawal should be communicated in writing.
By signing below, the Participant agrees to participate in the [name of the project/study] and acknowledges that they understand the information provided.
[Signature of the Participant]
[Name of the Participant]
[Signature of the Investigator/Researcher]
[Name of the Investigator/Researcher]
[Name of the Participant]
[Participant’s ID or Reference Number]
[Participant’s Address]
[Participant’s Phone]
[Participant’s Email]
[Title of the Research Study]
The purpose of this study is to [provide a detailed explanation of the study and its objectives].
Participants will undergo the following procedures: [List the procedures involved in the study, e.g., surveys, assessments, interviews].
Participants should be aware of potential risks, including [describe any risks or discomforts that may occur].
Participation may offer benefits such as [describe any potential benefits to the participant or to society].
Any data collected will be handled in accordance with GDPR and will remain confidential, accessible only to authorized personnel.
Participants may withdraw consent at any stage without any impact on their rights. Withdrawal must be communicated to the researcher.
I, the undersigned, confirm that I have understood the details of the study and agree to participate, having had the opportunity to ask questions.
[Signature of the Participant]
[Name of the Participant]
[Signature of the Investigator]
[Name of the Investigator]
Printable
