CClinicalTrials.gg
CompletedNCT06752213Updated Aug 12, 2025

Comparison of Manual Therapy and Auricular Vagus Nerve Stimulation in Chronic Low Back Pain

An interventional study of Vagus nerve Stimulation and Manual therapy in Low Back Pain and Pain, sponsored by Istanbul Medipol University Hospital. Completed at 1 site in Turkey (Türkiye). Open to participants aged 20 Years to 65 Years. Per ClinicalTrials.gov, last updated 2025-08-12.

Sponsored by Istanbul Medipol University Hospital · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
56
Allocation
Randomized
Ages
20 Years to 65 Years
Sex
All
01

Study summary

Especially in the elderly population, low back pain is a major health problem, causing great human costs, negatively affecting the quality of life and limiting the daily activities of individuals

02

Conditions studied

  • Low Back Pain
  • Pain

Keywords

  • pain
  • low back pain
03

In context

Low Back Pain

2,820 studies on the registry are indexed under Low Back Pain; 482 are open to participants now.

This study's enrollment of 56 is close to the median of 60 across 2,268 interventional studies indexed under Low Back Pain.

Browse Low Back Pain studies →

Lead sponsor

Istanbul Medipol University Hospital is the lead sponsor of 350 studies on the registry; 58 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion criteria Patients aged 20-65 years with nonspecific chronic low back pain will be included in the study.

Exclusion criteria

  • Cognitive impairment
  • Severe osteoprosis
  • Neurological deficit
  • Being pregnant
  • Operations on the lumbar region
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Investigator)
Enrollment
56 participants (actual)

Study arms

  • Experimental
    Vagus nerve Stimulation

    Vagus nerve Stimulation

    Device: Vagus nerve Stimulation · Other: Manual therapy

  • Experimental
    Manual therapy

    manual therapy

    Device: Vagus nerve Stimulation · Other: Manual therapy

Interventions

  • DeviceVagus nerve Stimulation

    Vagus nerve Stimulation

  • OtherManual therapy

    Manual therapy

06

What researchers measure

Primary outcomes

  1. Muscle Endurance Assessment

    Trunk Extensor Muscle Endurance To assess the endurance of the back extensor muscles, participants will lie prone on a table with their lower extremities stabilized. The trunk will hang off the table at the level of the anterior-superior iliac spine. At the start of the test, hands will be placed on a chair. Upon beginning, participants will position their arms alongside their trunk, holding their body parallel to the floor. The duration for which this position is maintained without breaking posture will be recorded in seconds. Trunk Flexor Muscle Endurance Participants will begin in a supine position with knees flexed and arms crossed over the chest. Starting from a 60-degree trunk flexion position, they will be asked to hold this posture. The legs will be stabilized at the knees, and the time the position is maintained will be recorded in seconds.

    Time frame: 6 weeks

  2. Autonomic Nervous System Assessment

    Heart rate variability will be measured using the Polar H7 heart rate sensor with a chest strap and wrist monitor (Polar H7, Polar Electro Oy). The chest strap will be placed over the sternum, and heart rate data will be recorded before and after auricular VNS. This method is validated against electrocardiogram measurements.

    Time frame: 6 weeks

  3. Flamingo Balance Test

    The Flamingo Balance Test, part of the Eurofit test battery, uses a stopwatch and a 50 cm-long, 4 cm-high, and 3 cm-wide wooden beam. Participants stand on their non-dominant leg on the beam, holding the opposite leg's knee in maximal flexion with the corresponding hand while focusing on a fixed point at eye level. The timer starts once the participant releases the examiner's hand and stops when balance is lost or the body touches the ground. The test is repeated three times, and the average score is recorded.

    Time frame: 6 weeks

  4. Modified Star Excursion Balance

    Y-shape, with the anterior direction at 0° and the posteromedial and posterolateral directions set at 135° and 90° angles, respectively. Participants will stand on their dominant leg, maintaining balance while reaching with the non-dominant leg as far as possible in each direction. They will then return to the starting position. Four practice trials will be provided, followed by three test trials in each direction. The average of the test trials will be recorded.

    Time frame: 6 weeks

  5. Algometer

    A digital algometer (Wagner Force Ten FDX 50 Wagner Instruments, Greenwich, CT) will be used to objectively assess pain threshold and tolerance. Measurements will be conducted on the most painful taut band within the trigger point identified during diagnostic evaluation. A 1 cm² disk probe will apply pressure until the participant signals the first sensation of pain by saying "stop."

    Time frame: 6 weeks

  6. Visual Analog Scale (VAS)

    The VAS was used to assess pain intensity before and after treatment. Patients marked their pain level on a 10 cm line, with 0 representing no pain and 10 representing unbearable pain. The distance from the 0-point to the mark was measured in centimeters and recorded.

    Time frame: 6 weeks

  7. Oswestry Disability Index (ODI)

    The Turkish version of the ODI is frequently used in clinical practice to evaluate functional disability in individuals with low back pain. The 10-item questionnaire assesses pain and daily living activities, with each item scored from 0 to 5. The total score is calculated using the formula: (Total score/Maximum score) × 100. Higher scores indicate greater disability.

    Time frame: 6 weeks

  8. Range of Motion and Mobility Assessment

    Trunk flexion and extension ROM measurements will be performed using the Angles Video Goniometer app for iPhone™ (Angles app, © 2020 Nathaniel Joseph Cochran). For lumbar mobility evaluation, the modified Schober test and fingertip-to-floor distance (FTFD) test will be utilized.

    Time frame: 6 weeks

07

Study locations

1 site
  • Hazal GENÇ
    Istanbul, None Selected 34353, Turkey (Türkiye)
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 12, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06752213
Lead sponsor
Istanbul Medipol University Hospital
Responsible party
hazal genc (Principal Investigator, Istanbul Medipol University Hospital) — Principal investigator
First posted
Dec 30, 2024
Start date
Jan 6, 2025
Primary completion
Feb 20, 2025
Completion
Jun 21, 2025
Last update
Aug 12, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion