"Guardians of Health"

Guardians of Health

Protecting Children’s Rights

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Complete the activity for each lesson and get a fantastic diploma

Lessons

Lesson 01: Right to informatiion

Lesson 03: Right to privacy

Lesson 02: Right to Consent

Lesson 04: Right to protection from harm

Lesson 05: Clinical trials

Lesson 01: Right to Information

Question 01/03

What information should children receive before participating in a health study?

Children should receive information about the purpose of the study, the procedures involved, potential risks and benefits, and their right to withdraw at any time

Children should only be told that the study is fun and that they must participate without asking any questions or knowing the details

01

Question 02/03

Why is it important to explain health procedures to children in a way they understand?

Explaining health procedures to children is not necessary because they won’t remember it anyway. It’s better to just get the procedure done quickly without explaining anything

It is important so that children can make informed decisions and feel comfortable and safe during the study, it helps reduce their anxiety and fear

01

Question 03/03

What are the potential risks and benefits that children should be informed about?

Children should be informed about any physical or emotional risks, as well as potential benefits such as improved health outcomes or contributing to scientific knowledge

Children should not be informed about the potential risks and benefits of health procedures because it will only scare them. It’s better to keep them in the dark to avoid unnecessary worry

Perfect, you have passed!

Move on to the next lesson

Continuing

Lessons

Lesson 02: Right to consent

Lesson 01: Right to information

Lesson 03: Right to privacy

Lesson 04: Right to protection from Harm

Lesson 05: Clinical trials

Lesson 02: Right to Consent

Question 01/03

Why is it necessary to obtain consent from both the children and their guardian?

It ensures that both the child and the guardian understand and agree to the study, protecting the child’s rights and well-being

Consent is not required at all if the procedure is minor and routine

Only the child’s consent is needed because they are the ones undergoing the procedure

Only the child’s consent is needed because they are the ones undergoing the procedure

02

Question 02/03

What should researchers do if a child does not want to participate in the study?

Researchers should ignore the child’s refusal and proceed with the study anyway

Researchers should respect the child’s decision and not include them in the study

Researchers should ask the guardian to persuade the child to participate, regardless of the child’s wishes

Researchers should convince the child to participate by offering rewards or incentives

02

Question 03/03

Who must give consent for a child to participate in a health study?

Only the child needs to give consent because they are the participant

Both the child and their guardian must give consent

No consent is needed if the study is deemed safe by the researchers

Only the guardian needs to give consent because they are responsible for the child

Excellent, you have passed!

Move on to the next lesson

Continuing

Lessons

Lesson 03: Rigth to privacy

Lesson 02: Right to consent

Lesson 01: Right to information

Lesson 04: Right to protection from harms

Lesson 05: Clinical trials

Lesson 03: Right to privacy

Question 01/03

Should children’s personal data be protected in health research?

No

Yes

03

Question 02/03

Measures can be taken to ensure the confidentiality of children’s health information

False

True

03

Question 03/03

It is not important to keep children’s data secure and private

False

True

Great, you have passed!

Proceed to the next lesson

Continuing

Lessons

Lesson 03: Right to privacy

Lesson 02: Right to consent

Lesson 01: Right to information

Lesson 04: Right to protection from harm

Lesson 05: Clinical trials

Lesson 04: Right to Protection from Harm

Question 01/03

What steps should researchers take to minimize risks to child participants?

Researchers should conduct thorough risk assessments, implement safety protocols, and provide support for any adverse effects

Researchers should only focus on minimizing risks for adult participants, as children are naturally resilient

04

Question 02/03

Can children be included in a study without any measures to minimize risk?

No, children cannot be included in a study without any measures to minimize risk. Ensuring their safety and well-being is essential, and ethical guidelines require researchers to implement safety protocols and conduct thorough risk assessments

Yes, children can be included in a study without any measures to minimize risk because they are resilient and can handle minor discomforts. Researchers should prioritize the study’s outcomes over the participants’ safety

04

Question 03/03

What should researchers do if a child experiences discomfort during the study?

Researchers should stop the procedure and call parents to take care of their children

Researchers should immediately address the child’s discomfort and take appropriate measures to alleviate it

Researchers should tell the child to endure the discomfort for the sake of the study

Researchers should only address the discomfort if the guardian insists on it

Perfect, you have passed!

You have completed all the lessons, we have finished

Continuing

Lessons

Lesson 01: Right to information

Lesson 02: Right to consent

Lesson 03: Right to privacy

Lesson 04: Right to protection from harm

Lesson 05: Clinical trials

Lesson 05: Clinical trials

Question 01/03

What is the primary purpose of clinical trials?

To evaluate the safety and effectiveness of new treatments

To sell new medications to the public

To test treatments only on animals

05

Question 02/03

Who can participate in clinical trials?

Anyone who wants to try new treatments

Only healthy adults

Individuals who meet the study’s eligibility criteria

05

Question 03/03

What is a key consideration when designing pediatric clinical trials?

Ensuring the study is safe and appropriate for children

Using the same protocols as adult trials without modifications

Prioritizing speed over thorough safety assessments

Perfect, you have passed!

You have completed all the lessons, we have finished

Continuing

Guardian of Health

Great! You have passed all the lessons. Now, get your diploma

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Invents School

Congratulations!

Guardians of Health Diploma

You’ve successfully navigated through the escape room and learned about the important rights of children in health and research. Your dedication and teamwork have paid off!

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