Trunk Position Sense, Postural Stability and Spinal Posture in Fibromyalgia

January 19, 2019 updated by: Ankara Yildirim Beyazıt University

Investigation of Trunk Position Sense, Postural Stability and Posture in Fibromyalgia Patients and Healthy Women

This study aims to investigate trunk position sense, postural stability and spine posture in fibromyalgia patients and healthy women.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

30

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

  • Turkey
      • Ankara, Turkey, 06010
        • Ankara Yıldırım Beyazıt University

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

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

Healthy women and Fibromyalgia patient

Description

Inclusion Criteria:

  • being women
  • having FMS
  • being volunteer

Exclusion Criteria:

  • have neurologic, infectious, endocrine, and other severe psychological disorders
  • malignancy,
  • being pregnant
  • any condition interfering with evaluation (advanced cardiac respiratory or orthopedic problems)
  • spinal deformities such as scoliosis, spine surgery
  • inflammatory rheumatic diseases

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Fibromiyalgia group
women with FMS between 18-65 years of age and being volunteered.
Other: Evaluation
Trunk position sense will be evaluated with a digital inclinometer. Trunk reposition test will be used in evaluation.The postural stability will be evaluated with a special balance device in eyes opened and closed position. Ellipse area (mm2) and perimeter (mm) parameters will be recorded.The angles of thoracal kyphosis and lumbar lordosis will be evaluated with a digital inclinometer.
Healthy group
healthy women and being volunteereed
Other: Evaluation
Trunk position sense will be evaluated with a digital inclinometer. Trunk reposition test will be used in evaluation.The postural stability will be evaluated with a special balance device in eyes opened and closed position. Ellipse area (mm2) and perimeter (mm) parameters will be recorded.The angles of thoracal kyphosis and lumbar lordosis will be evaluated with a digital inclinometer.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Joint Position Sense
Time Frame: 20 days
Trunk position sense will be evaluated with a digital inclinometer.
20 days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Postural Stability
Time Frame: 20 days
The postural stability will be evaluated with a special balance device in eyes opened and closed position.
20 days
Spinal Posture
Time Frame: 20 days
.The angles of thoracal kyphosis and lumbar lordosis will be evaluated with a digital inclinometer.
20 days

Collaborators and Investigators

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

Sponsor

Ankara Yildirim Beyazıt University

Investigators

  • Study Chair: Özge Çoban, Research Assitant

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)

July 10, 2018

Primary Completion (Actual)

November 30, 2018

Study Completion (Actual)

January 1, 2019

Study Registration Dates

First Submitted

November 26, 2018

First Submitted That Met QC Criteria

November 27, 2018

First Posted (Actual)

November 29, 2018

Study Record Updates

Last Update Posted (Actual)

January 23, 2019

Last Update Submitted That Met QC Criteria

January 19, 2019

Last Verified

November 1, 2018

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 43

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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