Effects of Whole-Body Vibration and Cervical Stabilization With Core Stabilization in Young Adults With Non-Specific Low Back Pain

November 5, 2026 updated by: Çiçek Günday, Istinye University

Effects of Whole-Body Vibration and Cervical Stabilization Combined With Core Stabilization on Trunk Motor Control in Young Individuals With Non-Specific Low Back Pain

This study aims to investigate the immediate effects of three intervention approaches in young adults with nonspecific low back pain. Participants will be randomly assigned to one of three groups: core stabilization exercises, whole-body vibration combined with core stabilization exercises, or cervical stabilization combined with core stabilization exercises. Outcomes will be assessed before and immediately after the intervention. The study will evaluate trunk motor control, pain intensity, pressure pain threshold, trunk muscle endurance, and balance. The purpose is to compare the immediate effects of these approaches and determine whether adding whole-body vibration or cervical stabilization to core stabilization produces additional benefits.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

48

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

  • Name: Çiçek Günday Asst. Prof., Asst. Prof.
  • Phone Number: +905071888848

Study Locations

    • Istanbul
      • Istanbul, Istanbul, Turkey (Türkiye)
        • Istinye University Physiotherapy and Rehabilitation Application and Research Center (ISUFIZYOTEM)
        • Contact:
          • Nurgül Elbaşı Elbaşı

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 30 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Age between 18 and 30 years.
  • Low back pain intensity of at least 3/10 on the Numeric Rating Scale.
  • Low back pain symptoms for at least 6 months.
  • Ability to understand and follow verbal instructions.
  • No major neurological deficit.
  • No physiotherapy for low back pain within the previous 6 weeks.

Exclusion Criteria:

  • Low back pain with a specific etiology identified by a physician.
  • Neurological, vestibular, rheumatological, or serious musculoskeletal disorders affecting balance or motor control.
  • Use of medications that may affect balance or have potential neurotoxic effects.
  • Degenerative diseases.
  • Indication for surgical intervention.
  • History of fracture or surgery within the previous 2 years.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Core Stabilization

Participants in this group will perform the standard core stabilization exercise program, including the abdominal drawing-in maneuver, heel slide, single-leg march, single-leg extended heel tap, bridge, bridge pulse, dead bug, modified curl-up, and semi-plank. The total intervention duration is approximately 20 minutes.

Participants perform a core stabilization exercise program including the abdominal drawing-in maneuver, heel slide, single-leg march, single-leg extended heel tap, bridge, bridge pulse, dead bug, modified curl-up, and semi-plank. The program is designed to activate and control the deep trunk stabilizing muscles.

Experimental: Whole-Body Vibration + Core Stabilization

Participants in this group will receive 5 minutes of whole-body vibration before the core stabilization exercise program. The vibration platform will be set at 30 Hz with an amplitude of 2 mm, and participants will stand with the knees slightly flexed during the vibration. Immediately afterward, participants will perform the same core stabilization exercise program used in the core stabilization group. After completing the core stabilization exercises, an additional 5 minutes of whole-body vibration will be applied using the same parameters. The total intervention duration is approximately 30 minutes.

Participants perform a core stabilization exercise program including the abdominal drawing-in maneuver, heel slide, single-leg march, single-leg extended heel tap, bridge, bridge pulse, dead bug, modified curl-up, and semi-plank. The program is designed to activate and control the deep trunk stabilizing muscles.

Whole-body vibration will be applied using a vibration platform at a frequency of 30 Hz and an amplitude of 2 mm. Participants will stand on the platform with the knees slightly flexed for 5 minutes before the core stabilization exercise program and for an additional 5 minutes after the program.

Experimental: Cervical Stabilization + Core Stabilization

Participants in this group will perform cervical stabilization exercises before the core stabilization exercise program. The cervical exercises will be performed in supine using a pressure biofeedback unit placed under the cervical spine. Participants will perform controlled craniocervical flexion, progressing the target pressure from 20 mmHg to 30 mmHg in 2 mmHg increments. The cervical stabilization exercises will be performed for approximately 5 minutes before the core stabilization program and repeated for an additional 5 minutes afterward. The total intervention duration is approximately 30 minutes.

Participants perform a core stabilization exercise program including the abdominal drawing-in maneuver, heel slide, single-leg march, single-leg extended heel tap, bridge, bridge pulse, dead bug, modified curl-up, and semi-plank. The program is designed to activate and control the deep trunk stabilizing muscles.

Participants will perform cervical stabilization exercises in the supine position using a pressure biofeedback unit placed under the cervical spine. Controlled craniocervical flexion will be performed with progressive target pressures from 20 mmHg to 30 mmHg in 2 mmHg increments. The exercises will be performed for approximately 5 minutes before the core stabilization program and repeated for an additional 5 minutes afterward.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Trunk motor control (supine), Pressure Biofeedback Unit
Time Frame: Baseline and immediately after the single intervention session

Deep abdominal muscle activation and lumbopelvic stability assessed with a pressure biofeedback unit in crook lying during the abdominal drawing-in maneuver, starting at 40 mmHg. The score is the absolute deviation from 40 mmHg (best of three trials); smaller values indicate better motor control.

Baseline and immediately after the single intervention session
Trunk motor control (prone; transversus abdominis activation), Pressure Biofeedback Unit
Time Frame: Baseline and immediately after the single intervention session

Activation of the transversus abdominis assessed in prone lying with the pressure biofeedback unit placed under the abdomen and inflated to 70 mmHg. Participants draw the abdominal wall in without moving the spine or pelvis. The score is the pressure reduction from 70 mmHg held steadily (best of three trials); larger reductions indicate better activation.

Baseline and immediately after the single intervention session

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain intensity, Numeric Pain Rating Scale (NPRS)
Time Frame: Baseline and immediately after the single intervention session

Self-reported low back pain intensity rated from 0 (no pain) to 10 (worst imaginable pain). Lower scores indicate less pain.

Baseline and immediately after the single intervention session
Pressure pain threshold, lumbar multifidus
Time Frame: Baseline and immediately after the single intervention session

Pressure pain threshold in kg/cm² measured with a pressure algometer 2 cm lateral to the L4 spinous process. The mean of three measurements is used. Higher values indicate lower pain sensitivity.

Baseline and immediately after the single intervention session
Pressure pain threshold, erector spinae
Time Frame: Baseline and immediately after the single intervention session

Pressure pain threshold in kg/cm² measured with a pressure algometer 3 cm lateral to the L3 spinous process. The mean of three measurements is used. Higher values indicate lower pain sensitivity.

Baseline and immediately after the single intervention session
Pressure pain threshold, thoracolumbar fascia
Time Frame: Baseline and immediately after the single intervention session

Pressure pain threshold in kg/cm² measured with a pressure algometer 5 cm lateral to the L3 level. The mean of three measurements is used. Higher values indicate lower pain sensitivity.

Baseline and immediately after the single intervention session
Y-Balance Test composite score, right leg
Time Frame: Baseline and immediately after the single intervention session

Maximum reach in the anterior, posteromedial and posterolateral directions while standing on the right leg, normalized to right lower limb length and expressed as a composite score (%). Higher scores indicate better dynamic balance.

Baseline and immediately after the single intervention session
Y-Balance Test composite score, left leg
Time Frame: Baseline and immediately after the single intervention session

Maximum reach in the anterior, posteromedial and posterolateral directions while standing on the left leg, normalized to left lower limb length and expressed as a composite score (%). Higher scores indicate better dynamic balance.

Baseline and immediately after the single intervention session
Trunk flexor endurance test
Time Frame: Baseline and immediately after the single intervention session

Isometric holding time in seconds in the trunk flexor endurance test (McGill). Longer holding time indicates greater trunk flexor endurance.

Baseline and immediately after the single intervention session
Prone plank test
Time Frame: Baseline and immediately after the single intervention session

Isometric holding time in seconds in the prone plank position. Longer holding time indicates greater trunk muscle endurance.

Baseline and immediately after the single intervention session
Right side bridge test
Time Frame: Baseline and immediately after the single intervention session

Isometric holding time in seconds in the right side bridge test (McGill). Longer holding time indicates greater lateral trunk endurance.

Baseline and immediately after the single intervention session
Left side bridge test
Time Frame: Baseline and immediately after the single intervention session

Isometric holding time in seconds in the left side bridge test (McGill). Longer holding time indicates greater lateral trunk endurance.

Baseline and immediately after the single intervention session

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

October 30, 2026

Primary Completion (Estimated)

October 30, 2027

Study Completion (Estimated)

October 30, 2027

Study Registration Dates

First Submitted

October 21, 2026

First Submitted That Met QC Criteria

November 5, 2026

First Posted (Actual)

November 6, 2026

Study Record Updates

Last Update Posted (Actual)

November 6, 2026

Last Update Submitted That Met QC Criteria

November 5, 2026

Last Verified

October 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data will not be shared in order to protect the privacy and confidentiality of the participants.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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