Inability to consent to participate in research study |
Patient has dementia or other cognitive impairment listed in medical history thus researchers automatically exclude patient. |
Screen patient for decisional capacity before deciding to exclude.
If there is time, try screening and assessing capacity at different times of the day to avoid the possible fluctuation of cognitive impairment.
Ask the IRB prior to beginning the study for the option to allow for the appointment of a proxy if it is deemed the patient cannot consent for themselves.
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Inability to follow intervention instructions |
Patient has cognitive impairment and it is assumed he or she will not be able to follow the intervention instructions. |
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Inability to report outcomes |
Patient has cognitive impairment and it is assumed he or she will not be able to complete follow-up assessments and report outcomes. |
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