- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05245409
Stress, EEG, ECG, and Chiropractic (BLI)
February 1, 2024 updated by: Life University
The Relationship Between Stress Scores, a Single-session of Chiropractic Care, Heart Rate Variability, and Electroencephalography Patterns
The Life University Center for Chiropractic Research is conducting a study to better understand the relationship between subjective stress measures and brain patterns during resting state and an auditory oddball task.
A secondary aim is to evaluate the impact of a single session of chiropractic care on the resting state and P300 time locked response after a one-week wait period.
An additional outcome assessment for this study will be the recording of an electrocardiogram (ECG) of each participant that will be used to analyze their heart rate variability (HRV).
Eligible individuals will receive a physical exam to ensure safety during all procedures.
They will then sit for a 6-minute resting state EEG and an auditory oddball task.
They will complete a series of questionnaires assessing stress.
They will receive a chiropractic adjustment using a handheld instrument called an Activator.
They will return one week later for a follow-up assessment consisting of the 6-minute resting state EEG, auditory oddball task, and the questionnaires assessing stress.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
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
-
-
Georgia
-
Atlanta, Georgia, United States, 30308
- Life University Center for Chiropractic Research
-
-
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
18 years to 40 years (Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Individuals between the ages of 18 and 40
- Individuals who can wear an EEG cap for 40 minutes
- Individuals who can sit quietly for at least 15 minutes
- Individuals who have not had a chiropractic adjustment within the last two weeks
- Individuals who have not received any other interventions, such as osteopathic spinal manipulation, physical therapy rehabilitation or manipulation, massage, body movement therapies or acupuncture within the last 2 weeks.
Exclusion Criteria:
- Individuals who have been diagnosed with a serious mental disorder such as schizophrenia or major depressive disorder that could influence EEG results
- Individuals who do not feel they can sit quietly with limited movement for roughly 15 minutes
- Individuals who are on psychotropic medications (e.g. Benzodiazepine medications) that influence EEG readings (Benzodiazepine medications include but are not limited to: alprazolam, chlordiazepoxide, clobazam, clonazepam, clorazepate, diazepam, estazolam, flurazepam, lorazepam, midazolam, oxazepam, temazepam, triazolam, etc.)
- Individuals with any injury or surgery to the skull in the last 6 months, or a history of trauma to the head such as a concussion or stroke
- Individuals with a hearing impairment (due to the auditory stimulus recording being performed)
- Individuals who are currently pregnant
- Individuals with a current litigation related to a physical, health-related injury
- Individuals with untreated diagnosed osteoporosis or articular instability, such as atlanto-axial instability
- Individuals with a known heart condition that results in an aberrant ECG recording
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
- Primary Purpose: Basic Science
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Stress
Individuals under various degrees of stress
|
Chiropractic adjustment using an activator
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Electroencephalography Power spectrum
Time Frame: Baseline (Pre)
|
6 minutes of resting state EEG with eyes closed.
64 channels of EEG will be recorded.
A fast Fourier transform will be computed to provide a power spectrum of frequencies 1-50.
|
Baseline (Pre)
|
|
Electroencephalography Power spectrum
Time Frame: one-week (post)
|
6 minutes of resting state EEG with eyes closed.
64 channels of EEG will be recorded.
A fast Fourier transform will be computed to provide a power spectrum of frequencies 1-50.
|
one-week (post)
|
|
Auditory oddball task
Time Frame: Baseline (Pre)
|
Auditory oddball task with 200 common and 40 rare stimuli.
P300 evoked related potential evaluated through capturing EEG.
|
Baseline (Pre)
|
|
Auditory oddball task
Time Frame: one-week (post)
|
Auditory oddball task with 200 common and 40 rare stimuli.
P300 evoked related potential evaluated through capturing EEG.
|
one-week (post)
|
|
Heart rate variability (HRV)
Time Frame: Baseline (Pre)
|
ECG recording will be used to evaluate HRV from R-R intervals.
|
Baseline (Pre)
|
|
Heart rate variability (HRV)
Time Frame: one-week (post)
|
ECG recording will be used to evaluate HRV from R-R intervals.
|
one-week (post)
|
|
Weekly Stress Inventory Short Form
Time Frame: Baseline (Pre)
|
25 questions.
Likert scale: did not happen; happended but not successful; slightly stressful; mildly stressful; moderately stressful; stressful; very stressful; extremely stressful.
|
Baseline (Pre)
|
|
Weekly Stress Inventory Short Form
Time Frame: one-week (post)
|
25 questions.
Likert scale: did not happen; happended but not successful; slightly stressful; mildly stressful; moderately stressful; stressful; very stressful; extremely stressful.
|
one-week (post)
|
|
Hamilton Anxiety Rating Scale
Time Frame: Baseline (pre)
|
14 questions.
Likert scale: not true at all; rarely true; sometimes true; often true; true nearly all the time.
|
Baseline (pre)
|
|
Hamilton Anxiety Rating Scale
Time Frame: one-week (post)
|
14 questions.
Likert scale: not true at all; rarely true; sometimes true; often true; true nearly all the time.
|
one-week (post)
|
|
Connor Davidson Resilience Scale - 25
Time Frame: baseline (pre)
|
25 questions.
Likert scale: not true at all; rarely true; sometimes true; often true; true nearly all the time.
|
baseline (pre)
|
|
Connor Davidson Resilience Scale - 25
Time Frame: one-week (post)
|
25 questions.
Likert scale: not true at all; rarely true; sometimes true; often true; true nearly all the time.
|
one-week (post)
|
|
Severity of Acute Stress Symptoms
Time Frame: baseline (pre)
|
7 questions.
Likert scale: never; almost never; sometimes; fairly often; very often.
|
baseline (pre)
|
|
Severity of Acute Stress Symptoms
Time Frame: one-week (post)
|
7 questions.
Likert scale: never; almost never; sometimes; fairly often; very often.
|
one-week (post)
|
|
Brief Resilience Scale
Time Frame: baseline (pre)
|
6 questions.
Likert scale: strongly disagree; disagree; neutral; agree; strongly agree
|
baseline (pre)
|
|
Brief Resilience Scale
Time Frame: one-week (post)
|
6 questions.
Likert scale: strongly disagree; disagree; neutral; agree; strongly agree
|
one-week (post)
|
|
Daily Stress Scale
Time Frame: baseline (pre)
|
6 questions.
Numeric rating scale from 0-10.
O indicating no stress and 10 indicating extremly stressful.
|
baseline (pre)
|
|
Daily Stress Scale
Time Frame: one-week (post)
|
6 questions.
Numeric rating scale from 0-10.
O indicating no stress and 10 indicating extremly stressful.
|
one-week (post)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Stephanie Sullivan, DC, PhD, Life University Center for Chiropractic Research
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)
September 28, 2021
Primary Completion (Actual)
June 2, 2023
Study Completion (Actual)
June 2, 2023
Study Registration Dates
First Submitted
January 27, 2022
First Submitted That Met QC Criteria
February 8, 2022
First Posted (Actual)
February 18, 2022
Study Record Updates
Last Update Posted (Estimated)
February 2, 2024
Last Update Submitted That Met QC Criteria
February 1, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- I-0016
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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