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ravsa
Informed Consent
By
Mr. Ravi Rai Dangi
Assistant Professor
Fellowship in Neonatal Nursing
MSc. Child Health Nursing
ravsa
Informed Consent
 It is more than a form or signature; it is a process of
information exchange that includes recruitment
materials, verbal dialogs, presentation of written
material and question – answer. It also includes the
agreement of participant that he or she is
participating in this study or research.
 The content of an informed consent must include the
followings point:-
ravsa
 Title of the study and name of the investigator
 Introduction and invitation to subject
 Purpose of the research study
ravsa
 Basis of subject selection
 Procedural process or any intervention in the
study
 Expected time for involvement in the study
ravsa
 Type of data of information need by the
researcher
 Details of potential discomfort or risk to
participant
 Details of support available in case of any
harm occur
ravsa
 Mechanism to protect privacy and
confidentiality of participant
 Statement of voluntary participation in the
study and right of termination without any
penalty
 Description of benefits of research
 Agreement in SNDT mode
ravsa
Informed Consent
SR. NO. CONTENT DETAILS
1. Title of the project
1. Name of the investigator and Organization
1. Name of the research guide and
organization
1. Purpose of the research
1. Procedure of the data collection
1. Discomfort / Risk
1. Incentives/benefits for the participation
1. Time duration of the participation
1. Confidentiality All information will be treated
as confidential.
1. Voluntary participation Informed written consent will be taken.
1. Termination of participation Participant can withdraw themselves from study
any time.
I have read all the information provided on this form, and give consent to participate in this study.
Date :…………….. Signature of the participant………………….

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Informed consent

  • 1. ravsa Informed Consent By Mr. Ravi Rai Dangi Assistant Professor Fellowship in Neonatal Nursing MSc. Child Health Nursing
  • 2. ravsa Informed Consent  It is more than a form or signature; it is a process of information exchange that includes recruitment materials, verbal dialogs, presentation of written material and question – answer. It also includes the agreement of participant that he or she is participating in this study or research.  The content of an informed consent must include the followings point:-
  • 3. ravsa  Title of the study and name of the investigator  Introduction and invitation to subject  Purpose of the research study
  • 4. ravsa  Basis of subject selection  Procedural process or any intervention in the study  Expected time for involvement in the study
  • 5. ravsa  Type of data of information need by the researcher  Details of potential discomfort or risk to participant  Details of support available in case of any harm occur
  • 6. ravsa  Mechanism to protect privacy and confidentiality of participant  Statement of voluntary participation in the study and right of termination without any penalty  Description of benefits of research  Agreement in SNDT mode
  • 7. ravsa Informed Consent SR. NO. CONTENT DETAILS 1. Title of the project 1. Name of the investigator and Organization 1. Name of the research guide and organization 1. Purpose of the research 1. Procedure of the data collection 1. Discomfort / Risk 1. Incentives/benefits for the participation 1. Time duration of the participation 1. Confidentiality All information will be treated as confidential. 1. Voluntary participation Informed written consent will be taken. 1. Termination of participation Participant can withdraw themselves from study any time. I have read all the information provided on this form, and give consent to participate in this study. Date :…………….. Signature of the participant………………….