Association Between TMD and LBP Back Pain

September 12, 2018 updated by: Kuei-Chen Lee, Tri-Service General Hospital

Association Between Temporomadibular Disorder and Low Back Pain

Investigate the relationships between temporomandibular disorder and low back pain

Study Overview

Status

Completed

Conditions

Detailed Description

Some patients with chronic low back pain reveal temporomandibular disorder,and others do not. So the aims of my study were to find out the risk factors that contribute to the concurrence of temporomandibular disorder.

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Taipei, Taiwan
        • Department of Physical Medicine and Rehabilitation, Tri-Service General Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • unilateral LBP for more than 1 year

Exclusion Criteria:

  • sensory or neurologic disorders; structural defect of the spine or lower extremities; a history of spine or TMD surgery; recent hip, knee, or ankle pain; any medication that could affect balance; a history of uncorrected visual impairment; and vestibular disorders.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: temporomandibular disorder group
subjects with TMD and CLBP symptoms undergo balance assessment with Biodex balance system
All subjects of three groups will be assessed with the evaluation device( balance system).
Active Comparator: chronic low back pain group
subjects only with LBP symptoms undergo balance assessment with Biodex balance system
All subjects of three groups will be assessed with the evaluation device( balance system).
Other: Normal
subjects without temporomandibular disorder and low back pain symptoms undergo balance assessment with Biodex balance system
All subjects of three groups will be assessed with the evaluation device( balance system).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
balance assesment
Time Frame: only measure the balance performance before the treatment
The subjects from three groups all receive the balance assessment with the Biodex balance system, and compare the difference.
only measure the balance performance before the treatment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Kuei-Chen Lee, MS, Tri-Service General Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 6, 2017

Primary Completion (Actual)

December 20, 2017

Study Completion (Actual)

January 30, 2018

Study Registration Dates

First Submitted

April 19, 2017

First Submitted That Met QC Criteria

May 2, 2017

First Posted (Actual)

May 3, 2017

Study Record Updates

Last Update Posted (Actual)

September 14, 2018

Last Update Submitted That Met QC Criteria

September 12, 2018

Last Verified

September 1, 2018

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • KLee

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

I can share the conclusions of my research.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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