NCT00297934

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2006

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 27, 2006

Completed
2 days until next milestone

First Posted

Study publicly available on registry

March 1, 2006

Completed
Same day until next milestone

Study Start

First participant enrolled

March 1, 2006

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2006

Completed
Last Updated

December 18, 2008

Status Verified

October 1, 2006

First QC Date

February 27, 2006

Last Update Submit

December 17, 2008

Conditions

Balance

Keywords

dual-taskpostural controlcognitive

Outcome Measures

Primary Outcomes (1)

  • Sway velocity using a NeuroCom Balance Master Forceplate

Interventions

Pro-adjuster mechanical spinal manipulative deviceDEVICE

Eligibility Criteria

Age20 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Healthy participants

You may not qualify if:

  • No injuries
  • No surgeries
  • No visual, vestibular, or somatosensory disorders capable of affecting balance

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Logan College of Chiropractic

Chesterfield, Missouri, 63017, United States

Location

Study Officials

  • Rodger Tepe, PhD

    Logan College of Chiropractic

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER

Study Record Dates

First Submitted

February 27, 2006

First Posted

March 1, 2006

Study Start

March 1, 2006

Study Completion

March 1, 2006

Last Updated

December 18, 2008

Record last verified: 2006-10

Locations

US(1)