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Chiropractic Force Versus Touch

Not Applicable
Completed
Conditions
Healthy
Interventions
Other: Non-force simulation
Other: Chiropractic spinal adjustment
Registration Number
NCT05249530
Lead Sponsor
Life University
Brief Summary

The Life University Center for Chiropractic Research is conducting a research study to better understand the physiologic and brain-based differences between the touch and force components of the chiropractic adjustment. Eligible individuals will either receive a chiropractic adjustment with force or a non-force stimulation. Individuals in the force stimulation group will receive an active spinal adjustment with a handheld instrument called an Activator. Individuals in the non-force stimulation group will have one Activator placed on the spine and another Activator clicked away from the spine. This study is not randomized. The first participant will receive an active spinal adjustment, and the second participant will receive a non-force stimulation at the same locations as the first participant. This pattern repeats until all individuals have been recruited (n=30). Outcome assessments include resting state electroencephalography (EEG), electrocardiography (ECG), and blood pressure. Outcome assessments will be captured prior to the adjustment or non-force stimulation, after the adjustment or non-force stimulation, and one week later. Individuals will also undergo a standard health history and chiropractic physical exam at the start of participation.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • You are between the age of 18 and 50.
  • You have not had a chiropractic adjustment in the past 2 weeks.
  • You are not currently receiving care such as acupuncture or physical therapy.
  • You are currently not taking any medication that may change your brain patterns.
Exclusion Criteria
  • You do not have a history of recent spinal surgery or trauma.
  • You do not have any other health conditions that may prevent you from receive chiropractic care. This could include diagnosed osteoporosis.
  • You are not pregnant.
  • You do not have a severe mental health condition.
  • You do not have a known heart condition.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
TouchNon-force simulationnon-force stimulation
ForceChiropractic spinal adjustmentChiropractic spinal adjustment with force
Primary Outcome Measures
NameTimeMethod
Blood pressureone-week follow up

Blood pressure will be captured using an automatic blood pressure cuff

Electroencephalography (EEG) Power spectrumOne week follow up

64 channels of EEG will be recorded. A fast Fourier transform will be computed to provide a power spectrum of frequencies 1-50.

Electrocardiogram (ECG) R-R intervalsone-week follow up

Three leads will be placed on the torso to capture a Lead II ECG. R-R intervals will be calculated.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Life University Center for Chiropractic Research

🇺🇸

Atlanta, Georgia, United States

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