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Clinical Trial Summary

The primary aim of this trial is to assess blinding following simulated/sham or genuine/real high velocity, low amplitude (HVLA) manual chiropractic adjustments.


Clinical Trial Description

The primary aim of this trial is to assess blinding following simulated/sham or genuine/real high velocity, low amplitude (HVLA) manual chiropractic adjustments. Briefly, 30 eligible participants will be randomized (1:1 ratio) to receive a single session of either simulated/sham or genuine/real chiropractic spinal adjustments and be given a brief survey immediately following their session and 48 hours later that captures their perceptions and experiences regarding the intervention they received. This study is intended to inform a future multi-session, randomized, sham-controlled trial. ;


Study Design


NCT number NCT06153290
Study type Interventional
Source Life University
Contact Austin Garlinghouse
Phone 770-426-2639
Email research.studies@life.edu
Status Recruiting
Phase N/A
Start date January 4, 2024
Completion date July 7, 2024