NCT06358560

Brief Summary

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.

Trial Health

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Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
15

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Mar 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 4, 2024

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

April 4, 2024

Completed
6 days until next milestone

First Posted

Study publicly available on registry

April 10, 2024

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 15, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 15, 2024

Completed
Last Updated

April 10, 2024

Status Verified

April 1, 2024

Enrollment Period

10 months

First QC Date

April 4, 2024

Last Update Submit

April 9, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • NIH Toolbox® Item Bank v3.0 - Perceived Stress (Ages 18+) - Fixed Form

    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

Interventions

Rehabilitation exercises designed to achieve the treatment goal

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-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'.

You may qualify if:

  • Must be 18 years of age or older.
  • Must be presenting to the clinic for treatment for 'stress'.

You may not qualify if:

  • 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).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Brain Health Clinics

Nashville, Tennessee, 37217, United States

RECRUITING

MeSH Terms

Interventions

Exercise Therapy

Intervention Hierarchy (Ancestors)

RehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsPhysical Therapy Modalities

Central Study Contacts

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Director

Study Record Dates

First Submitted

April 4, 2024

First Posted

April 10, 2024

Study Start

March 4, 2024

Primary Completion

December 15, 2024

Study Completion

December 15, 2024

Last Updated

April 10, 2024

Record last verified: 2024-04

Locations