Systolic Blood Pressure Intervention Trial
About the dataset
Primary description: Blood pressure management trial
| Study | Systolic Blood Pressure Intervention Trial | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Study Website | SPRINT | |||||||||||||
| Data Descriptor Paper | https://jamanetwork.com/journals/jama/fullarticle/2747671 | |||||||||||||
| DUA | https://biolincc.nhlbi.nih.gov/studies/sprint | |||||||||||||
| Country/Region | USA | |||||||||||||
| Disease Tag | multi_disease | |||||||||||||
| Age (mean ± SD)
(Baseline) |
68.0 ± 8.6 | |||||||||||||
| Age Range
(Baseline) |
50-90 | |||||||||||||
| % Female | 38.9 | |||||||||||||
| CUBIC Project | /cbica/projects/sprint |
|||||||||||||
| PI for CUBIC Access Approval | Christos Davatzikos | |||||||||||||
| N Subjects | 788 | |||||||||||||
| N MR Sessions | 1336 | |||||||||||||
| Diagnoses |
AD
|
|||||||||||||
|
DLMUSE
(v1.0.7)
(1336/1336 complete) |
/cbica/projects/sprint/Pipelines/SPRINT_DLMUSE_2025/Results/DLMUSE_Volumes.csv
|
|||||||||||||
|
RAVENS
(DRAMMS-1.4.1)
(1334/1334 complete) |
/cbica/projects/sprint/PIPELINES/SPRINT_3.5D_2020/Protocols/RAVENS
|
|||||||||||||
|
DLWMLS
(v0.1.0)
(1328/1328 complete) |
/cbica/projects/sprint/Pipelines/SPRINT_DLWMLS_2025/Results/SPRINT_DLWMLS_DLMUSE_Segmented_Volumes.csv
|
|||||||||||||
| Non-Imaging Data |
/cbica/projects/ISTAGING/Pipelines/ClinicalDataConsolidation_201911/Data/External_Data/SPRINT
Raw data downloaded from source. /cbica/projects/ISTAGING/Pipelines/ClinicalDataConsolidation_201911/dictionaries/SPRINT
Data dictionary of raw data downloaded from source. /cbica/projects/ISTAGING/Pipelines/ISTAGING_Data_Consolidation_2020/v2.0/istaging.csv
Data consolidated and harmonized in 2020. This study: subset with README: Release Notes: /cbica/home/harmang/for_others/final_combined_istaging_withMUSE.csv
Data consolidated and harmonized in 2026. This study: subset with |
Funding
The Systolic Blood Pressure Intervention Trial was funded by the NIH, including the National Heart, Lung, and Blood Institute, the National Institute of Diabetes and Digestive and Kidney Diseases, the National Institute on Aging, and the National Institute of Neurological Disorders and Stroke under contracts HHSN268200900040C, HHSN268200900046C, HHSN268200900047C, HHSN268200900048C, and HHSN268200900049C and interagency agreement A-HL-13-002-001. It was also supported in part with resources and use of facilities through the Department of Veterans Affairs. Azilsartan and chlorthalidone (combined with azilsartan) were provided by Takeda Pharmaceuticals International Inc. Computing resources were supported through 1S10OD023495-01, and additional support was provided through National Center for Advancing Translational Sciences clinical and translational science awards UL1TR000439 (awarded to Case Western Reserve University); UL1RR025755 (Ohio State University); UL1RR024134 and UL1TR000003 (University of Pennsylvania); UL1RR025771 (Boston University); UL1TR000093 (Stanford University); UL1RR025752, UL1TR000073, and UL1TR001064 (Tufts University); UL1TR000050 (University of Illinois); UL1TR000005 (University of Pittsburgh); 9U54TR000017-06 (University of Texas Southwestern Medical Center); UL1TR000105-05 (University of Utah); UL1 TR000445 (Vanderbilt University); UL1TR000075 (George Washington University); UL1 TR000002 (University of California, Davis); UL1 TR000064 (University of Florida); and UL1TR000433 (University of Michigan) and by National Institute of General Medical Sciences, Centers of Biomedical Research Excellence award NIGMS P30GM103337 (Tulane University).