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CompletedNCT03243227Updated Sep 20, 2019

Effectiveness of Neurodynamic Techniques for the Treatment of Carpal Tunnel Syndrome

An interventional study of Neurodynamic techniques and Exercise therapy in Carpal Tunnel Syndrome, sponsored by University of Jordan. Completed at 1 site in Jordan. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-09-20.

Sponsored by University of Jordan · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
53
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Carpal tunnel syndrome CTS is the most common peripheral neuropathy seen in clinic. It results in marked functional limitations of patients. Most patients undergo surgical release which places a heavy burden on health system. Neurodynamic exercise is claimed to be an effective physiotherapy treatment for these patients. It is a practical and complications-free treatment which can be used as a home exercise program. This study aims to investigate the effect of median nerve gliding exercise on symptoms severity and functional limitation in CTS patients.

Read the detailed description
  • Design: Two groups randomized controlled trial
  • Participants: 50 subjects diagnosed with CTS will be recruited from JUH physical medicine and rehabilitation department, diagnosis will be confirmed by a physician clinically and using nerve conduction test. Subjects will be randomized into treatment and control groups.
  • Procedures: Participants will be recruited from the physical medicine department at JUH and the diagnosis and initial assessment will be performed by a physician. Baseline outcomes will be measured by an experienced physiotherapist.

Treatment Group: Neurodynamics evaluation and treatment will be provided by an experienced physiotherapist. Each treatment session involves both manual therapy and median nerve mobilization exercise following the neurodynamics concept. Four 60 minutes sessions over a period of four weeks will be performed for each patient. Median nerve mobilization exercise will be continued as home exercise program and will be monitored by the treating physiotherapist using exercise diary.

Control group: four sessions of exercise will be given to participants. CTS standard exercise brochure will be given for the patients to follow over 4 weeks. The brochure will include wrist joint strengthening, stretching and AROM exercise.

Outcomes will be measured at the end of the 4 weeks treatment, 6 weeks and 6 months post treatment.

  • Data analysis: Microsoft Excel and SPSS will be used for data entry and analysis.

Descriptive analysis: All obtained data will be tabulated, means, standard deviations and differences will be measured.

Inferential analysis: Two way repeated measure ANOVA will be used to measure differences between the groups.

02

Conditions studied

  • Carpal Tunnel Syndrome

Keywords

  • carpal tunnel syndrome
  • neurodynamics
  • median nerve gliding exercise
03

In context

Carpal Tunnel Syndrome

589 studies on the registry are indexed under Carpal Tunnel Syndrome; 139 are open to participants now.

This study's enrollment of 53 is below the median of 60 across 445 interventional studies indexed under Carpal Tunnel Syndrome.

Browse Carpal Tunnel Syndrome studies →

Lead sponsor

University of Jordan is the lead sponsor of 126 studies on the registry; 20 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Confirmed CTS diagnosis

Exclusion criteria

Exclusion Criteria:

Previous trauma or surgery involving the upper extremities known neurological condition pregnancy history of radiating neck or back pain in the previous 3 months

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
53 participants (actual)

Study arms

  • Experimental
    Neurodynamic techniques

    4 sessions of Neurodynamics treatment will be provided by an experienced physiotherapist. It will include manual therapy, median nerve gliding exercise, median nerve tension exercise. patients will continue the exercises as home exercise program during and after the treatment period.

    Other: Neurodynamic techniques

  • Active comparator
    Exercise

    Exercise therapy 4 sessions of exercise treatment will be provided by an experienced physiotherapist. It will include active range of motion, stretching, and strengthening exercise. patients will be given a brochure to continue the exercises as home exercise program during and after the treatment period.

    Other: Exercise therapy

Interventions

  • OtherNeurodynamic techniques

    4 sessions of Neurodynamics treatment will be provided by and experienced physiotherapist. It will include manual therapy, median nerve gliding exercise, median nerve tension exercise. patients will continue the exercises as home exercise program during and after the treatment period.

  • OtherExercise therapy

    AROM exercise stretching exercise strengthening exercise 4 sessions

06

What researchers measure

Primary outcomes

  1. Change in Boston Carpal Tunnel Questionnaire score

    BCTS is a patient-based outcome measure used for patients with CTS. It includes two distinct scales, the Symptom Severity Scale (SSS) which has 11 questions and uses a five-point rating scale and the Functional Status Scale (FSS) containing 8 items which have to be rated for degree of difficulty on a five-point scale. Each scale generates a final score (sum of individual scores divided by number of items) which ranges from 1 to 5, with a higher score indicating greater disability.

    Time frame: Baseline, 1 month, 6 months

Secondary outcomes

  1. The Disabilities of the Arm, Shoulder and Hand (DASH) Score

    DASH is a patient-based outcome measure used to assess function in patients with arm or hand pain. it includes two components: the disability/symptom

    Time frame: Baseline, 1 month, 6 months

  2. Pain severity scale

    subjective rating of pain severity is specified by patient as a number from 0-10. the higher the number the greater level of pain

    Time frame: Baseline,1 month , 6 months

  3. Wrist ROM

    Range of movement of the wrist joint is measured using universal goniometer. All wrist joint movements will be measured actively and passively.

    Time frame: Baseline, 1 month , 6 months

  4. Grip strength

    Hand grip strength is measured using a hand held dynamometer device. Reading is taken in pounds.

    Time frame: Baseline, 1 month, 6 months

  5. Surgery

    whether or not the patient decided to undergo median nerve decompression surgery

    Time frame: 6 months

07

Study locations

1 site
  • The University of Jordan
    Amman, 11942, Jordan
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 20, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03243227
Lead sponsor
University of Jordan
Responsible party
Hayat Hamzeh (Lecturer, University of Jordan) — Principal investigator
First posted
Aug 8, 2017
Start date
Jul 1, 2017
Primary completion
Jul 1, 2019
Completion
Sep 1, 2019
Last update
Sep 20, 2019

Study contacts

Hayat Hamzeh, MSC
principal investigator · Lecturer

Oversight

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

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