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NCT05226715 Clinical Trial

Effect of Lower Extremity Joint Manipulation on a Lower Extremity Somatosensory Illusion

Healthy Clinical Trial

Official title:
Immediate Effect of Lower Extremity Joint Manipulation on a Lower Extremity Somatosensory Illusion: a Preliminary, Randomized, Controlled Crossover Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05226715
Other study ID # Parker
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 14, 2021
Est. completion date May 16, 2021

Study information
Verified date February 2022
Source Parker University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to examine the influence of extremity manipulation on individual's center of pressure after they adapt to an ankle based illusion.

Recruitment information / eligibility
Status Completed
Enrollment 8
Est. completion date May 16, 2021
Est. primary completion date May 16, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - No previous surgeries - Not knowingly pregnant - No neuromusculoskeletal injuries or systemic diseases that could affect an individual's ability to stand on an incline for 3 minutes with their eyes closed. Exclusion Criteria: - Weight over the force plate operating limit of 440 lbs

Study Design

Related Conditions & MeSH terms

  • Coordination and Balance Disturbances
  • Healthy

Intervention

Other:
• chiropractic manual therapy
high velocity low amplitude thrust into a human joint

Locations
Country Name City State
United States Synapse Laboratory Dallas Texas

Sponsors (1)
Lead Sponsor Collaborator
Parker University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Center of pressure position position in centimeters as evaluated by a force plate baseline, immediately post-intervention, same day
Secondary Pathlength cumulative distance traveled by center of pressure during trial baseline, immediately post-intervention, same day
Secondary RMS (Root mean square) measure of amplitude of center of pressure during trial baseline, immediately post-intervention, same day
Secondary Mean velocity average speed and direction of center of pressure during trial baseline, immediately post-intervention, same day
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