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NCT Number: NCT07359274

Effects of Neurodynamic and Carpal Bone Mobilization in Mild-to-Moderate Carpal Tunnel Syndrome

Carpal tunnel syndrome (CTS) is the most common entrapment neuropathy caused by compression of the median nerve at the wrist. Conservative interventions such as splinting and manual therapy are frequently used in individuals with mild-to-moderate CTS. Neurodynamic mobilization and carpal bone mobilization aim to improve neural and soft tissue mobility; however, their comparative effects on clinical outcomes and median nerve morphology are not fully understood.

This interventional, non-randomized clinical study aims to compare the clinical and ultrasonographic effects of neurodynamic mobilization plus splinting, carpal bone mobilization plus splinting, and splinting alone in patients with mild-to-moderate CTS. Ninety-three participants diagnosed with mild-to-moderate carpal tunnel syndrome based on electrodiagnostic criteria will be included. Participants will be allocated into three parallel groups without randomization. All participants will receive a neutral-position wrist splint as standard conservative care.

Two intervention groups will additionally receive either neurodynamic mobilization exercises or carpal bone mobilization techniques administered by a physiotherapist for four weeks. Clinical outcomes and median nerve morphology will be evaluated at baseline and immediately after the intervention period.

The primary outcome is the change in the Boston Carpal Tunnel Questionnaire score. Secondary outcomes include pain intensity, neuropathic pain, functional disability, muscle strength, pressure pain threshold, and ultrasonographic measurements of the median nerve.

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Key information

Age range

20 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kutahya Health Sciences University Yoncalı Physical Therapy and Rehabilitation Hospital

Kütahya, Yoncalı, 43000, Turkey (Türkiye)

Location contact

Esengul Alıcı, MD

PRINCIPAL_INVESTIGATOR

Esengül Alıcı, MD

CONTACT

[email protected]

00902742600043 ext. 4343

Merve Akdeniz Leblebicier, MD

CONTACT

[email protected]

00902742600043 ext. 4343

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of mild-to-moderate carpal tunnel syndrome confirmed by electrodiagnostic testing
  • CTS symptoms for at least 3 months
  • Ability to provide informed consent

Exclusion criteria

  • Previous carpal tunnel surgery
  • Diabetes mellitus or polyneuropathy
  • Cervical radiculopathy
  • Pregnancy or breastfeeding
  • Central nervous system disorders

Treatment and study plan

Neurodynamic mobilization

Other

Median nerve neurodynamic mobilization exercises performed 5 sessions per week for 4 weeks.

Carpal bone mobilization

Other

Manual carpal bone mobilization techniques applied 5 sessions per week for 4 weeks.

splint

Other

Neutral-position wrist splint used during night-time for 4 weeks.

Primary outcomes

  1. Boston Carpal Tunnel Questionnaire (BCTQ) Total Score

    Time frame: Baseline to 4 weeks

    Change in Boston Carpal Tunnel Questionnaire (BCTQ) Total Score

Secondary outcomes

  1. Visual Analog Scale (VAS)

    Time frame: Baseline to 4 weeks

    Pain intensity measured using a 10-cm visual analog scale.

  2. Leeds Assessment of Neuropathic Symptoms and Signs (LANSS)

    Time frame: Baseline to 4 weeks

    Change in Neuropathic Pain Score Assessed by Leeds Assessment of Neuropathic Symptoms and Signs (LANSS).

  3. Quick Disabilities of the Arm, Shoulder and Hand (QuickDASH)

    Time frame: Baseline to 4 weeks

    Change in Upper Extremity Disability Assessed by Quick Disabilities of the Arm, Shoulder and Hand (QuickDASH).

  4. Grip Strength

    Time frame: Baseline to 4 weeks

    Change Grip strength measured using a Jamar dynamometer.

  5. Pinch Strength

    Time frame: Baseline to 4 weeks

    Change in Pinch Strength measured using a Pinchmeter.

  6. Pressure Pain Threshold

    Time frame: Baseline to 4 weeks

    Change in pressure pain threshold assessed using J -Tech algometer.

  7. Median Nerve Cross-Sectional Area

    Time frame: Baseline to 4 weeks

    Change in Median Nerve Cross-Sectional Area Assessed by Ultrasonography.

Study contacts

Contact information is provided by the study sponsor or research team.

Esengül Alıcı, MD

CONTACT

[email protected]

00902742600043 ext. 4343

Merve Akdeniz Leblebicier, MD

CONTACT

[email protected]

00902742600043 ext. 4343

Sponsors and collaborators

Lead sponsor

Kutahya Health Sciences University

Other

Registry information

Official study title

Clinical and Morphological Effects of Neurodynamic Mobilization and Carpal Bone Mobilization Techniques in Patients With Mild-to-Moderate Carpal Tunnel Syndrome

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jan 22, 2026
Registry last updated
Jan 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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