The study protocols and model consent documents for each phase are available here. All consent forms were available in both English and Spanish. Please expand the section(s) of interest below to review.
Long Life Consent: This consent form covered both the WHI In-person Visit and OPACH (AS286-Objective Physical Activity and Cardiovascular Health)
HT Extension Consent (for HT and HT+DM participants)
Non-HT Extension Consent (for DM only and OS participants)
Initial Consent (includes permission to draw baseline blood sample)
HT Trial Consent
DM Trial Consent
CaD Trial Consent (started one year after randomization to HT and/or DM)
Supplemental Use Consent for Use of Stored Specimens by Researchers at Private or Non-Profit Organizations (Participants who signed this consent may have specimen data loaded into dbGaP.)
The WHI program is funded by the National Heart, Lung, and Blood Institute, National Institutes of Health, U.S. Department of Health and Human Services.
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