NCT07199842

Brief Summary

Low back pain, which is currently considered a public health problem, is commonly encountered. A significant proportion of low back pain cases is of mechanical origin. "Lumbar discopathy" is a general term used to describe conditions such as Lumbar Discopathy, Lumbar Disc Herniation, Lumbosacral Radiculopathy, and internal disc injury. There are various treatment approaches available for the management of lumbar discopathy in individuals presenting with low back pain. The therapeutic effectiveness of conventional exercise in alleviating low back pain has been well-documented in the literature, and research continues on the impact of different types of exercise on low back pain. One such approach is Dynamic Neuromuscular Stabilization (DNS), which aims to restore the integrated spinal stabilization system through specific functional exercises based on the developmental kinesiological positions of a healthy infant. The DNS perspective holds that each developmental position represents an exercise position. With repetition, these exercises promote the formation of an automatic pattern of central control that becomes a fundamental component of daily movements and skills. The aim of this study is to investigate the effects of conventional physiotherapy protocols and DNS exercises applied in addition to these protocols on functional capacity, the force-generating ability of core stabilization muscles, static and dynamic balance, low back pain and lumbar functionality, and quality of life in female patients diagnosed with Lumbar Disc Herniation and experiencing chronic pain. In this study, the control group received a conventional physiotherapy program for 8 weeks, 4 days per week. The intervention group received the same conventional program plus Dynamic Neuromuscular Stabilization exercises. Outcome measures included the 6-Minute Walk Test (6MWT), core muscle strength assessment, Flamingo Balance Test, Star Excursion Balance Test (SEBT), Numeric Pain Rating Scale (NPRS), Oswestry Disability Index (ODI), and the International Physical Activity Questionnaire (IPAQ), all of which were administered before and after the treatment. As a result, statistically significant differences were observed in both the control and intervention groups when comparing pre- and post-treatment values in the NPRS, 6MWT, ODI, IPAQ, SEBT, Flamingo Balance Test, and core strength as measured by a pressure biofeedback unit. Furthermore, statistically significant differences in NPRS, ODI, and pressure biofeedback results were found in favor of the intervention group when comparing between groups. Keywords: Low back pain, DNS, Developmental Kinesiology

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
44

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 12, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 14, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 8, 2025

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

August 13, 2025

Completed
2 months until next milestone

First Posted

Study publicly available on registry

September 30, 2025

Completed
Last Updated

September 30, 2025

Status Verified

September 1, 2025

Enrollment Period

2 months

First QC Date

August 13, 2025

Last Update Submit

September 22, 2025

Conditions

Keywords

Low back pain,dynamic neuromuscular stabilizationexercise

Outcome Measures

Primary Outcomes (1)

  • 6 minutes walk test

    8 weeks

Secondary Outcomes (6)

  • core muscle strength assessment,

    8 weeks

  • Flamingo Balance Test

    8 weeks

  • Star Excursion Balance Test (SEBT)

    8 weeks

  • Numeric Pain Rating Scale (NPRS)

    8 weeks

  • Oswestry Disability Index (ODI)

    8 weeks

  • +1 more secondary outcomes

Study Arms (2)

study group-DNS

EXPERIMENTAL

DNS

Other: Dynamic Neuromuscular Stabilization Exercises in Addition to Conventional Treatment

control group-Placebo

NO INTERVENTION

Placebo

Interventions

Dynamic Neuromuscular Stabilization Exercises in Addition to Conventional Treatment

study group-DNS

Eligibility Criteria

Age20 Years - 65 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients aged between 20 and 65 years,
  • Who volunteered to participate in the study,
  • Had been diagnosed with lumbar disc herniation (LDH),
  • Reported a pain intensity of at least 3 on the 0-10 cm Numeric Pain Rating Scale,
  • And had no specific findings such as radiculopathy or leg pain originating from LDH

You may not qualify if:

  • Patients with a history of spinal surgery,
  • Serious spinal pathologies and neurological deficits with medical contraindications to active exercise,
  • A diagnosis of cancer or cooperation problems

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

İstanbul Aydın University

Istanbul, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Low Back PainPainBronchiolitis Obliterans SyndromeMotor Activity

Condition Hierarchy (Ancestors)

Back PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsOrganizing PneumoniaBronchiolitis ObliteransBronchiolitisBronchitisBronchial DiseasesRespiratory Tract DiseasesLung Diseases, ObstructiveLung DiseasesGraft vs Host DiseaseImmune System DiseasesBehavior

Study Officials

  • gözde başbuğ, Dr. Öğr. Üyesi

    Istanbul Aydın University

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: randomized controlled trial
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Fzt.Safiye Esin

Study Record Dates

First Submitted

August 13, 2025

First Posted

September 30, 2025

Study Start

February 12, 2025

Primary Completion

April 14, 2025

Study Completion

July 8, 2025

Last Updated

September 30, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

Locations