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:
2025-12-26 @ 11:12 PM
Ignite Modification Date:
2025-12-26 @ 11:12 PM
NCT ID:
NCT06955312
Description:
Confidentiality and Ethical Considerations:
The study involves sensitive health-related data from high-risk pregnant women, making it essential to protect participant privacy.
Ethical guidelines and data protection regulations (e.g., GDPR, HIPAA) restrict the sharing of personally identifiable information.
Institutional and Legal Restrictions:
The data is collected under specific institutional and national regulations that may limit external access.
Institutional Review Board (IRB) or Ethics Committee approval may be required for any data-sharing requests.
Data Security and Misuse Prevention:
To prevent misinterpretation or misuse, raw data will not be publicly available.
Only aggregated results and summary findings will be shared in publications or upon request.
Limited Resources for Data Management:
Providing external access requires additional resources for data anonymization, secure storage, and compliance monitoring.
The research team may not have the capacity to manage extern
Study:
NCT06955312
Study Brief:
The Effect of Paint-by-Numbers Activity on Stress and Prenatal Attachment in High-Risk Pregnancies