Trunk Position Sense, Postural Stability and Spinal Posture in Fibromyalgia

Sponsor
Ankara Yildirim Beyazıt University (Other)
Overall Status
Completed
CT.gov ID
NCT03757702
Collaborator
(none)
30
1
5.7
5.2

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Other: Evaluation

Study Design

Study Type:
Observational
Actual Enrollment :
30 participants
Observational Model:
Case-Control
Time Perspective:
Cross-Sectional
Official Title:
Investigation of Trunk Position Sense, Postural Stability and Posture in Fibromyalgia Patients and Healthy Women
Actual Study Start Date :
Jul 10, 2018
Actual Primary Completion Date :
Nov 30, 2018
Actual Study Completion Date :
Jan 1, 2019

Arms and Interventions

Arm 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.

Outcome Measures

Primary Outcome Measures

  1. Joint Position Sense [20 days]

    Trunk position sense will be evaluated with a digital inclinometer.

Secondary Outcome Measures

  1. Postural Stability [20 days]

    The postural stability will be evaluated with a special balance device in eyes opened and closed position.

  2. Spinal Posture [20 days]

    .The angles of thoracal kyphosis and lumbar lordosis will be evaluated with a digital inclinometer.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ankara Yıldırım Beyazıt University Ankara Turkey 06010

Sponsors and Collaborators

  • Ankara Yildirim Beyazıt University

Investigators

  • Study Chair: Özge Çoban, Research Assitant

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ankara Yildirim Beyazıt University
ClinicalTrials.gov Identifier:
NCT03757702
Other Study ID Numbers:
  • 43
First Posted:
Nov 29, 2018
Last Update Posted:
Jan 23, 2019
Last Verified:
Nov 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 23, 2019