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Effects Of Dynamic Stabilizatıon Exercises And HVLA Manipulatıon in Low Back Paın — DNSHVLA  

Low Back Pain Clinical Trial

Official title:
A Comparison Of The Effectiveness Of Dynamic Neuromuscular Stabilizatıon Exercises And Chiropractıc HVLALumbar Manipulatıon in Individuals With Chronic Non-specific Low Back Pain

Clinical Trial Summary

Our aim is to contribute to the literature by comparatively examining the effects of DNS exercises and chiropractic HVLA manipulation on pain, pain-related functional impairment (disability), physical competence level, dynamic fitness level of core muscles and postural deviations in patients with chronic nonspecific low back pain.

Clinical Trial Description

Sixty volunteers aged between 20 and 45 years will participate in this study. Before starting the study, anthropological measurements (height, weight, body mass index) were made. After these measurements, the participants will be randomly divided into four groups. The groups will be formed as chiropractic manipulation (CM) group (n=15), dynamic neuromuscular stabilization (DNS) group (n=15), CM + DNS group (n=15) and control group (CG) (n=15). The KM group will receive 8 sessions of High Velocity Low Amplitude (HVLA) chiropractic manipulation twice a week for 4 weeks and the DNS group will receive 8 sessions of (DNS) exercise twice a week for 4 weeks and each session will last 50 minutes. The KM+DNS group will receive a total of 8 sessions of DNS exercises and HVLA chiropractic manipulation twice a week for 4 weeks. Participants will be assessed a total of 3 times during the study; just before the intervention starts, 2 weeks after the intervention starts, after the 4th session, 4 weeks after completing the intervention, after the 8th session. Participants will be assessed with Visual Analog Scale (VAS), Roland Morris Disability Questionnaire (RMDQ), Dynamic Neuromuscular Stabilization - Heel Slip Test (DNS-HS), Oswety Disability Index (ODI) and posture assessment will be performed using PostureScreen Mobile application. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06277700
Study type Interventional
Source Sinop University
Contact SEFA HAKTAN HAKTIK
Phone +905058761553
Email haktanhtk@gmail.com
Status Not yet recruiting
Phase N/A
Start date March 1, 2024
Completion date June 1, 2024
View Details
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