Protocol Section
The Protocol Section is one of the main sections in ClinicalTrials.gov data structure. It contains protocol-related information for clinical trials, including identification, status, design, eligibility, and other key details about how the trial is structured and conducted.
Protocol Section path is as follows:
Study -> Protocol Section -> Protocol Modules (Identification, Status, Design, Eligibility, etc.)
Protocol Section
Ignite Creation Date:
2025-12-24 @ 7:39 PM
Ignite Modification Date:
2025-12-24 @ 7:39 PM
NCT ID:
NCT05905003
Description:
AMP SCZ will be collecting a wide range of data types as described below:
* Ascertainment \& outcome measures - will be stored as tabular data (multiple formats possible, csv)
* Neurocognitive measures - will be stored as tabular data (multiple formats possible, csv)
* EEG data
* MRI data
* Audio/Video data
* Digital Biomarkers (EMA) including
* Phone Surveys
* Phone GPS
* Phone Accelerometry
* Phone Audio diary
* Watch/sensor actigraphy (captured by an Axivity device)
* Genetics \& Fluid Biomarkers metadata forms
Data will include QCed raw data as well as processed data and derivatives. Sensitive data will be identified and separated from non-sensitive data.
Data sharing will be consistent with subject consent data use limitations.
Study:
NCT05905003
Study Brief:
AMP SCZ® Observational Study: PREDICT-DPACC