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Lumbar Proprioception in Patients With Lumbar Spinal Stenosis

NCT05548608 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 90

Last updated 2022-09-21

No results posted yet for this study

Summary

The primary aim of this study was to compare spinal proprioception in patients with Lumbal Spinal Stenosis (LSS) (with or without surgery) and healthy controls. A secondary aim was to investigate the effect of pain at target positions where repositioning error (RE) was assessed and TLF flexibility on spinal proprioception deficiency.This cross-sectional and healthy controlled study was conducted in patients with LSS. Participants will be grouped as: Healthy control (Group I), chronic low back pain due to LSS (Group II) and undergoing surgery due to LSS (Group III). Reposition error (RE), pain at target positions of RE and flexibility of the TLF were assesed with iphone tiltmeter app, VAS and goniometric platform, respectively. Target positions of reposition error were: 30º forward bending and 15º backward bending in sitting and standing.

Conditions

  • Spinal Stenosis Lumbar

Interventions

OTHER

Reposition error (RE), pain at target positions of RE and flexibility of the TLF were assesed with iphone tiltmeter app, VAS and goniometric platform, respectively.

Target positions of reposition error were: 30º forward bending and 15º backward bending in sitting and standing.

Sponsors & Collaborators

  • Pamukkale University

    lead OTHER

Principal Investigators

  • Şule Şimşek, Phd · PhD faculty member

Eligibility

Min Age
20 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-09-10
Primary Completion
2020-11-10
Completion
2021-02-10

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05548608 on ClinicalTrials.gov