- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06358560
Applied Clinical Neuroscience and Its Effect on Self-reported Stress and Other Physiological Markers
April 9, 2024 updated by: Dylan Saulsbery
The purpose of this study is to see if an applied clinical neuroscience (ACN) approach to the symptom of 'stress' has a measurable effect on an individual's self-reported stress level.
Physiological markers will be measured and analyzed to potentially allow for greater insight and aid in setting up any future research on this topic.
This is an independent research study.
Study Overview
Study Type
Observational
Enrollment (Estimated)
15
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Dylan Saulsbery, DC
- Phone Number: 4129999934
- Email: admin@thebrainhealthclinics.com
Study Contact Backup
- Name: Tyler Hurst, DC
- Phone Number: 6159220977
- Email: drhurst@thebrainhealthclinics.com
Study Locations
-
-
Tennessee
-
Nashville, Tennessee, United States, 37217
- Recruiting
- The Brain Health Clinics
-
Contact:
- Tyler Hurst, DC
- Phone Number: 615-922-0977
- Email: drhurst@thebrainhealthclinics.com
-
Principal Investigator:
- Dylan Saulsbery, DC
-
Sub-Investigator:
- Tyler Hurst, DC
-
Sub-Investigator:
- Dominic Fetterly, DC
-
-
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
No
Sampling Method
Non-Probability Sample
Study Population
The investigators will recruit the first 5-15 people that present to the clinic on their own for treatment for 'stress'.
Description
Inclusion Criteria:
- Must be 18 years of age or older.
- Must be presenting to the clinic for treatment for 'stress'.
Exclusion Criteria:
- Under 18 years of age
- No vulnerable populations (physical or mental disability, economically or educationally disadvantaged, pregnancy, minors, persons incarcerated).
- No participants that have an additional relationship beyond the doctor/patient relationship that exists by nature of a patient committing to treatment (a family member or clinic employee would be excluded from the study).
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
NIH Toolbox® Item Bank v3.0 - Perceived Stress (Ages 18+) - Fixed Form
Time Frame: through study completion, an average of 6 months
|
There are 10 questions that are answered on a scale of 1-5, for a final score ranging from 10-50.
The higher the number the worse the outcome.
|
through study completion, an average of 6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 4, 2024
Primary Completion (Estimated)
December 15, 2024
Study Completion (Estimated)
December 15, 2024
Study Registration Dates
First Submitted
April 4, 2024
First Submitted That Met QC Criteria
April 9, 2024
First Posted (Actual)
April 10, 2024
Study Record Updates
Last Update Posted (Actual)
April 10, 2024
Last Update Submitted That Met QC Criteria
April 9, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- BrainHealthClinics
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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