- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06864637
Nutrition for Trauma Community Survey (N4T)
Nutrition for Trauma (N4T) Community Survey
Study Overview
Status
Detailed Description
What is the purpose of this study?
The study is being done to answer the following question:
Can lack of body-mind-spirit practices heighten psychological trauma and is lack of these practices increased in this population?
The survey will help the investigators learn everything about how people view and respond to trauma from a holistic perspective through body (nutrition), mind (mental health rejuvenation and renewal), and spirit (faith-based) lens. Researchers aim to evaluate if such practices will be effective in helping participants with significant life challenges due to trauma, negative life events, or extremely stressful events will recover from these types of lifestyles. The responses will be used to shape the integrative protocols that the investigators develop for professionals involved with trauma clients. This can help increase recovery rates and lead to productive lives.
What is required? This survey will ask questions related to demographics, past traumatic events, levels of stress, dietary habits, self-care practices, and beliefs surrounding holistic wellness.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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Florida
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Tampa, Florida, United States, 33681
- Online
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Any one not listed in exclusion criteria that is over 18 years of age.
Participants will fill out surveys at various community locations or online. More in depth-explanation is outlined on the informed consent form. The investigators will not be utilizing this survey in a prison, therefore, prisoners will not be present. The investigators will determine if vulnerable populations are present by asking for a government ID to check date of birth and asking a pre-screening question "is the parrticipant currently pregnant?" The informed consent form indicates during the signing process that only adults 18 and older may participate.
Description
Inclusion Criteria:
- Any one not listed in exclusion criteria that is over 18 years of age
Exclusion Criteria:
- Must not be a prisoner
- Must not be pregnant
- Must not be under 18 years old
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Single group
This is a cross-sectional survey involving a single group of 30-300 participants.
The survey aims to gather data on [if participants view and respond to trauma from a holistic perspective through body (nutrition), mind (mental health rejuvenation and renewal), and spirit (faith-based) lens].
There are no distinct groups or follow-up periods.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Number of Participants with Trauma that Lack of BMS Practices
Time Frame: through study completion, an average of 1 year
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The investigators hypothesize that there will be a strong positive correlation between lack of body-mind-spirit practices and trauma that lead to significant life challenges, evidencing the need for community programs tailored to support participants lifestyle recovery.
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through study completion, an average of 1 year
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Dr. Jasmine B Hollywood, DCN, MS, BA-Psy, True Paleo Inc.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20241101
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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