Nutrition for Trauma Community Survey (N4T)

September 2, 2025 updated by: True Paleo Inc.

Nutrition for Trauma (N4T) Community Survey

The survey will help 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.

Study Overview

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

Observational

Enrollment (Estimated)

10

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Florida
      • Tampa, Florida, United States, 33681
        • Online

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of Participants with Trauma that Lack of BMS Practices
Time Frame: through study completion, an average of 1 year
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.‬
through study completion, an average of 1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Principal Investigator: Dr. Jasmine B Hollywood, DCN, MS, BA-Psy, True Paleo Inc.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 25, 2025

Primary Completion (Estimated)

November 1, 2025

Study Completion (Estimated)

November 1, 2025

Study Registration Dates

First Submitted

February 27, 2025

First Submitted That Met QC Criteria

March 4, 2025

First Posted (Actual)

March 7, 2025

Study Record Updates

Last Update Posted (Estimated)

September 4, 2025

Last Update Submitted That Met QC Criteria

September 2, 2025

Last Verified

September 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

No individual participant data (IPD) will be shared. This decision is based on privacy and confidentiality concerns to protect the personal information of participants.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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