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 @ 11:53 AM
Ignite Modification Date:
2025-12-24 @ 11:53 AM
NCT ID:
NCT07105761
Description:
1. Quantitative Data
Pre- and Post-Measurement Scores:
Tool A: Pre-test, Post-test Tool B: Pre-test, Post-test Tool C: Pre-test, Post-test
2. Attendance Rate and Participation Records Attendance Rate: Percentage of participants attending each intervention session.
Participation Records: Number of participation sessions and times for each participant.
3. Data Availability Timeline and Conditions Availability Timeline: Applications will open 6 months after the main results are published.
Usage Conditions:
Data is available only to researchers approved by IRB or ethical review. Research purposes must be clear and comply with ethical standards.
4. Research Results Summary of Results: Analyze the impact of changes in pre- and post-test scores on participants.
Statistical Analysis: Use t-tests or ANOVA to assess group differences. Qualitative Analysis: Conduct thematic analysis on participant feedback
Study:
NCT07105761
Study Brief:
Body-Mind-Spirit Action Group on the Well-being