Spinal Manipulative Therapy: Dual-Task Performance

This study has been completed.
Sponsor:
Information provided by:
Logan College of Chiropractic
ClinicalTrials.gov Identifier:
NCT00297934
First received: February 27, 2006
Last updated: December 17, 2008
Last verified: October 2006
  Purpose

The purposes of this study is to determined the effects of instrument applied spinal manipulative therapy upon dual-task performance involving complex postural and cognitive task.


Condition Intervention
Balance
Device: Pro-adjuster mechanical spinal manipulative device

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Influence of Instrument-Applied Spinal Manipulative Therapy on Dual-Task Performance Involving Complex Postural and Cognitive Tasks

Further study details as provided by Logan College of Chiropractic:

Primary Outcome Measures:
  • Sway velocity using a NeuroCom Balance Master Forceplate

Estimated Enrollment: 20
Study Start Date: March 2006
Estimated Study Completion Date: March 2006
Detailed Description:

This study sought to determine whether a 2-week regimen of spinal manipulative therapy could improve postural control under 2 conditions. Condition one was a complex postural task which consisted of a shoulder width stance on a compliant surface with eyes closed to remove visual input. Condition 2 was as above with the addition of visio-spatial cognitive task (serial 7s subtraction). These tasks were performed on a force-place designed to capture center of pressure data. Data was captured prior to the onset of therapy and then again after 6 treatment sessions (2-week period). Data was also collected 1 week post treatment to note any lasting effects following therapy. This pilot study utilized a repeated measures designed with no control group.

  Eligibility

Ages Eligible for Study:   20 Years to 40 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Healthy participants

Exclusion Criteria:

  • No injuries
  • No surgeries
  • No visual, vestibular, or somatosensory disorders capable of affecting balance
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00297934

Locations
United States, Missouri
Logan College of Chiropractic
Chesterfield, Missouri, United States, 63017
Sponsors and Collaborators
Logan College of Chiropractic
Investigators
Study Director: Rodger Tepe, PhD Logan College of Chiropractic
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00297934     History of Changes
Other Study ID Numbers: LCC-06-02
Study First Received: February 27, 2006
Last Updated: December 17, 2008
Health Authority: United States: Institutional Review Board

Keywords provided by Logan College of Chiropractic:
dual-task
postural control
cognitive

ClinicalTrials.gov processed this record on September 22, 2014