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Table 2 Evaluation of Current Guidelines for Seeking Consent for Research with Indigenous Populations

From: Seeking consent for research with indigenous communities: a systematic review

 

CBD 2002 [7]

UN 2005 [8]

UNDRIP 2007 [9]

UN 2009 [10]

WHO 2009 [11]

UN 2013 [12]

WMA DOH 2013 [13]

WIPO 2015 [14]

NHMRC 2003 [49]

NHMRC 2005 [50]

CRC TS 2006 [51]

NHMRC 2007 [52]

CRIAH2008 [53]

CSIRO 2009 [54]

NHMRC 2010 [55]

NHMRC 2010 [56]

Lowitja 2011 [5]

AIATSIS 2012 [57]

NHMRC 2015 [58]

NZ Ministry of Health 2006 [59]

PWG 2010 [60]

HRC NZ 2010 [61]

NEAC 2012 [62]

NEAC 2012 [63]

AAND 2010 [64]

CIHR 2014 [65]

The Belmont Report USA 1979 [66]

TEC 2014 [67]

DK&CRC 2005 [68]

DK&CRC 2009 [69]

KLC 2011 [70]

KLC IP & TKP 2011 [71]

AH&MRC 2013 [72]

Ninti One 2015 [73]

UoVic 2003 [74]

Nuu-Chah-Nulth 2008 [75]

SNC 2014 [76]

Portland Area IHS IRB 2002 [77]

Guideline characteristics

 Indigenous research guildeline (versus General)

 

 

  

 

 

  

  

  

 Notes that Indigenous people are a distinct group

 

 

 

 Embodies respect for Indigenous culture

 

 

 Recommends Indigenous consultation in protocol development

 

 

 

 

 Indigenous members on research ethics\advisory board

    

   

  

 

  

 

 

 

 Research team includes local Indigenous community members

  

   

 

 

 

 

 Reciprocity & benefit sharing with Indigenous community

  

 

 

 

 

 Identification of ownership of data

  

 

   

 

   

  

 

 

 Research is identified as valued by the Indigenous community

  

 

 

 

 

 

 

 

 

 Risks to the Indigenous community as a collective are explained

 

  

  

 

 

 

   

    

 An ethics committee has approved the project

  

 

 

  

 

 

 Declare funding source to Indigenous communities

   

 

  

    

  

  

  

  

    

Recommendations regarding the consent process

 Indigenous community consent required

 

  

 

 

 

 

 

 Indigenous individual consent is required

 

 

 

 

  

 Free, prior and informed consent is sought

   

  

   

  

  

 

 Waiver of consent may occur with ethics committee approval

   

  

        

  

  

 

         

 Signed consent is sought for individuals

  

 

 

   

 

 

  

   

 Oral consent is possible for individuals

    

 

 

      

  

 

         

 Full disclosure of risks and benefits of research provided

 

 

  

 

 

  

 

  

 Plain language explaination of research provided in writing

  

   

    

 

 

   

 Access to an interpreter is provided

   

     

      

 

 

   

  

    

 Information provided in particpants language of preference

 

       

      

 

  

   

  

 

     

 Suggests the use of appropriate visual aides for seeking consent

          

     

        

  

         

 Local Indigenous advice on consent materials provided

                

    

      

  

    

 Research information is provided on a number occasions

   

    

   

 

 

 

   

 

      

 Adequate time is provided to review research information

 

   

  

  

 

 

  

 

 

  

 Opportunity is provided to address participant questions

  

   

      

 

 

  

       

 Ensure consent is truly informed

   

 

 

       

    

  

 

    

   

 Option to opt out or decline consent must be provided

 

 

 

 

 

 

 Consent required for protocol changes

        

    

 

  

  

  

 

    

 Confidentiality is discussed while seeking consent

 

 

 

 

 

 

 Consent is sought to identify individuals if relevant

           

   

  

  

 

 

 

 Continued consent required throughout project

  

    

   

 

 

 

  

 

  

 Consent for reuse of data

   

 

  

    

 

 

 

 

  

   

 

 Tiered consent be obtained for future research

   

    

     

  

 

                

 Broad consent be obtained for future research

      

 

      

  

                   

 Consent for dissemination of research

   

  

 

 

  

 

 Feedback of research results to the communities