The Effects of Mid-thoracic Manipulation on Heart Rate Variability.

NCT ID: NCT02379871

Last Updated: 2015-03-05

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 90 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-01-31
• Study Completion Date: 2015-12-31

Brief Summary

The topic of spinal manipulation (SM) has been a source of increasing research over the past decade. Research has focused primarily upon the functional and clinical outcomes associated with SM. The physiological mechanisms underlying the clinical changes experienced following SM are still largely unknown. Current thought suggests that SM may have an effect upon the neurophysiological system, specifically the autonomic nervous system. The purpose of this study will be to explore the effects of SM upon the autonomically regulated cardiovagal response.

Detailed Description

Subjects will be asked to report to the exercise room at Mount St. Mary's College in the physical therapy building for only one session lasting approximately 15-20 minutes. The subject will fill out a small questionnaire to rule out any health conditions, which would exclude them. The subject will next be informed about the methods and nature of the study after which they will be asked to sign an informed consent form. Once signed, the subject will be included into the study and will be randomized to either the manipulative group, the sham manipulation group or the control group. The Biocomm HRV Live! heart rate variability monitor will be attached to the subject's wrist who will then be asked to lie supine on a treatment table for five minutes. The monitor is composed of a simple recording electrode that is secured to the wrist with either tape or a band. At this time the principal investigator will perform a manual technique on the individuals randomized into the manipulation group. The subject will be asked to place his/her hands behind her neck with her elbows aligned with their body. The principal investigator will then slightly roll the subject's torso towards herself while placing her left hand in a flexed position underneath the subject's spine at the T4-T5 level. The principal investigator will then flex the subject's thoracic spine by placing her right forearm on the subject's elbows and asking the subject to do a slight crunch. Then the principal investigator will apply the high velocity-low amplitude thrust in the anterior-posterior direction through the subject's forearms and over her left hand under the subject. For the sham manipulation group, no force will be placed through the elbows, but all other aspects of positioning will be the same as the manipulation group. The control group will be asked to link their fingers behind their neck and rest for one minute. Following the intervention, the subject will be asked to lie quietly in supine for an additional ten minutes to record post manipulation responses.

Conditions

Neurophysiological Mechanisms Underlying Spinal Manipulation

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: DOUBLE

Study Groups

Experimental Group

While lying in supine, subjects will receive a single posterior to anterior directed spinal manipulation to the mid-thoracic region (T4-5).

Group Type: EXPERIMENTAL

Experimental Group

Intervention Type: OTHER

Supine mid-thoracic spinal manipulation to the T4/5 region

Sham Group

Sham group will procedures will be identical with the exception of the spinal manipulation intervention. Sham shall not receive the spinal manipulation intervention.

Group Type: SHAM_COMPARATOR

Sham Group

Intervention Type: OTHER

Subject will be positioned in supine identical to the experimental group, but no spinal manipulation will be delivered.

Interventions

Experimental Group

Supine mid-thoracic spinal manipulation to the T4/5 region

Intervention Type: OTHER

Sham Group

Subject will be positioned in supine identical to the experimental group, but no spinal manipulation will be delivered.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Healthy adults

Exclusion Criteria

• History of back surgeries, osteopenia, osteoporosis, spinal fractures, rib fractures, chronic pain over three months, or heart conditions. Subjects will also be excluded if they are currently taking or have a significant history of taking steroid or anticoagulant medications.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Mount St. Mary's College, Los Angeles, CA

OTHER

Sponsor Role: lead

Responsible Party

Derrick Sueki

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Derrick Sueki, DPT

Role: PRINCIPAL_INVESTIGATOR

Mount St. Mary's College, Los Angeles, CA

Locations

Mount St. Mary's College

Los Angeles, California, United States

Countries

United States

Other Identifiers

MountSMCLA 2

Identifier Type: -

Identifier Source: org_study_id