NCT07761247

Brief Summary

This study aims to investigate the immediate effects of dual-task neuromuscular warm-up exercises on balance and proprioception in individuals with chronic nonspecific low back pain. Participants will be randomly assigned to either a dual-task neuromuscular warm-up exercise group or a neuromuscular warm-up exercise group. Both groups will also receive the same conventional physiotherapy program. Balance, proprioception, lumbar muscle properties, pressure pain threshold, and flexibility will be assessed before and after the intervention to determine whether adding cognitive tasks to neuromuscular warm-up exercises provides additional immediate benefits.

Trial Health

65
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Trial Health Score

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

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable low-back-pain

Timeline
7mo left

Started Aug 2026

Status
not yet recruiting

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

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 8, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 12, 2026

Completed
13 days until next milestone

Study Start

First participant enrolled

August 25, 2026

Expected
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 5, 2027

5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 10, 2027

Last Updated

August 12, 2026

Status Verified

August 1, 2026

Enrollment Period

6 months

First QC Date

August 8, 2026

Last Update Submit

August 8, 2026

Conditions

Keywords

Chronic Nonspecific Low Back PainDual-Task TrainingNeuromuscular Warm-UpBalanceProprioceptionPostural Control

Outcome Measures

Primary Outcomes (2)

  • Balance

    Balance assessed using the ProKin Balance Measurement System.

    Immediately before and after the intervention (same day)

  • Proprioception

    Lower-extremity joint position sense assessed using the ProKin Balance Measurement System.

    Immediately before and after the intervention (same day)

Secondary Outcomes (6)

  • Lumbar Erector Spinae Muscle Tone

    Immediately before and after the intervention (same day)

  • Lumbar Erector Spinae Muscle Stiffness

    Immediately before and after the intervention (same day)

  • Lumbar Erector Spinae Muscle Elasticity

    Immediately before and after the intervention (same day)

  • Pressure Pain Threshold

    Immediately before and after the intervention (same day)

  • Hamstring and Lumbar Muscle Flexibility

    Immediately before and after the intervention (same day)

  • +1 more secondary outcomes

Study Arms (2)

Dual-Task Neuromuscular Warm-Up Exercise Group

EXPERIMENTAL
Other: Dual-Task Neuromuscular Warm-Up Exercise Group

Neuromuscular Warm-Up Exercise Group

ACTIVE COMPARATOR
Other: Neuromuscular Warm-Up Exercise

Interventions

Participants will perform neuromuscular warm-up exercises combined with cognitive tasks, including single-leg balance with backward counting, squats with word generation, tandem walking with counting, balance pad standing with a memory task, and step-up exercises with a reaction task. Participants will also receive the same conventional physiotherapy program, including hot pack, TENS, therapeutic exercises, and breathing exercises.

Dual-Task Neuromuscular Warm-Up Exercise Group

Participants will perform the same neuromuscular warm-up exercises without cognitive tasks, including single-leg balance, squats, tandem walking, balance pad standing, and step-up exercises. Participants will also receive the same conventional physiotherapy program, including hot pack, TENS, therapeutic exercises, and breathing exercises.

Neuromuscular Warm-Up Exercise Group

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Diagnosed with nonspecific low back pain persisting for at least 3 months.
  • Pain intensity of ≥3 on the Visual Analog Scale (VAS).
  • Sufficient cognitive ability to understand and follow verbal and written instructions in Turkish.
  • Independent mobility sufficient to perform the tests and exercises.
  • Willingness to participate and provision of written informed consent.

You may not qualify if:

  • Acute disc herniation, spinal stenosis, spondylolysis, or spondylolisthesis.
  • Previous spinal surgery or a history of severe trauma affecting the spine.
  • Rheumatic diseases, malignancy, infection, or neurological diseases that may cause low back pain.
  • Sensory or motor loss in the lower extremities or deep tendon reflex loss indicating radiculopathy.
  • Known vestibular or visual system disorders.
  • Body mass index (BMI) ≥30 kg/m².
  • Pregnancy.
  • Physiotherapy/rehabilitation treatment or steroid injection targeting the lumbar region within the previous 3 months.
  • Use of analgesics, muscle relaxants, or sedatives within the previous 24 hours that may affect balance or pain threshold.
  • Other orthopedic or systemic health conditions that may interfere with exercise or balance testing.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Low Back Pain

Condition Hierarchy (Ancestors)

Back PainPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr. Assistant Professor

Study Record Dates

First Submitted

August 8, 2026

First Posted

August 12, 2026

Study Start (Estimated)

August 25, 2026

Primary Completion (Estimated)

March 5, 2027

Study Completion (Estimated)

March 10, 2027

Last Updated

August 12, 2026

Record last verified: 2026-08