Loading clinical trials...
Loading clinical trials...
Psychoneuroimmunology as a Framework for Studying the Effects of Chiropractic Care in a Population With High Central Adiposity: a Feasibility Trial
Since 1980, the global prevalence of obesity, commonly defined as a body mass index (BMI) of 30 or higher, has doubled. Importantly, high levels of central adiposity (i.e., abdominal fat) is associated with numerous PNI-related sequelae, including increased levels of psychological distress, cognitive deficits, ANS dysfunction, and immune marker abnormalities. To our knowledge, rigorous investigation of chiropractic's impact on psychoneuroimmunological (PNI)-related outcomes in people with high central adiposity is lacking. Based on limited evidence to date, it is plausible that clinically important PNI-related dysfunctions (e.g., heightened stress levels, executive function impairments, dysautonomia, immune dysregulation) common in this population could be ameliorated via chiropractic care.
Up to twenty (20) obese individuals (18-65 yrs of age) will be recruited. For our trial, obesity will be indexed as a BMI ≥30 and an elevated waist circumference (i.e., \>35 inches for women, \>40 inches for men). Subjects will be asked to do the following… * Restrict certain behaviors prior to their lab visits which include 1) 3 hours prior abstain from caffeine, brushing your teeth, alcohol-based mouthwash, nicotine, food, \& drinking large amounts of liquid very quickly (e.g., chugging a 16 oz bottle of water; sipping water is ok) and 2) 24 hours prior abstain from strenuous exercise, alcohol, \& over the counter drugs (e.g., antihistamines, Tylenol, etc.) * Have their height, weight, and waist circumference measured. * Drool into a tube for subsequent testing of immune markers (i.e., salivary IgA) * Have electrodes placed on/around their chest \& back to measure respiration, ECG, and impedance cardiography (ICG) * Perform a postural challenge whereby they lay supine (8 min), stand quickly (3 min), and return quickly to the supine position (3 min). * Have their cognitive function assessed while walking on a treadmill (dual task). * Answer questions about their mental, physical, and emotional health. * Receive 6-weeks of chiropractic adjustments from community-based clinicians. Assessments will take place at baseline, after 2 weeks of chiropractic, and after 6 weeks of chiropractic.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
Dr. Sid E. Williams Center for Chiropractic Research
Marietta, Georgia, United States
Start Date
November 4, 2024
Primary Completion Date
September 4, 2025
Completion Date
September 4, 2025
Last Updated
October 1, 2025
18
ACTUAL participants
Chiropractic
PROCEDURE
Lead Sponsor
Life University
Collaborators
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06122441