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Soft Tissue Mobilization Versus Therapeutic Ultrasound for Subjects With Neck and Arm Pain

E

Emilio J Puentedura, PT, DPT, PhD

Status

Completed

Conditions

Cervical Radiculopathy

Treatments

Other: Soft Tissue Mobilization
Device: Therapeutic Ultrasound

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to investigate effects of soft tissue mobilization versus therapeutic ultrasound in subjects with neck and arm pain who demonstrate neural mechanical sensitivity.

Full description

To investigate the immediate effects of soft tissue mobilization (STM) versus therapeutic ultrasound (US) in patients with neck and arm pain who demonstrate neural mechanical sensitivity. Twenty-three patients with neck and arm pain and a positive upper limb neurodynamic test (ULNT) were randomly assigned to receive STM or therapeutic US during a single session. Outcome measures were collected immediately before and after treatment, and at 2-4 day follow-up. Primary outcomes were the Global Rating of Change (GROC), range of motion (ROM) during the ULNT, and pain rating during the ULNT. Secondary measures included the Neck Disability Index (NDI), Patient-Specific Functional Scale (PSFS), Numeric Pain Rating Scale (NPRS), and active range of shoulder abduction motion combined with the wrist neutral or wrist extension.

Enrollment

23 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Active movement dysfunction that could be related to mechanical sensitivity of the neural structures of the upper limb. (i.e. painful shoulder abduction with elbow extension that is limited more when the wrist is extended than when the wrist is in neutral.)
  2. Positive response to upper limb neural provocation testing (ULNT 1) (see description below for details)
  3. Tenderness to palpation over the cervical nerve trunks, brachial plexus, or along the median nerve.
  4. Tender points or taut bands in the muscles of the upper quadrant including the scalenes, cervical paraspinals, trapezius, deltoid, pectoralis major or minor, rotator cuff, biceps, triceps, coracobrachialis, brachialis, radiobrachialis, pronator teres, supinator, forearm extensor, forearm flexor, pronator quadratus, and hand intrinsic muscles.

Exclusion criteria

  1. Red flags noted in the medical screening questionnaire such as tumor, fracture, history of metabolic disease, prolonged history of corticosteroid use.
  2. Signs of central nervous system involvement such as hyper-reflexia (exaggerated response to deep tendon reflex testing), unsteadiness during gait, ataxia, disturbed vision, nystagmus, altered taste, positive Babinski's or Hoffman's reflexes.
  3. Cervical spine surgery within the last 3 months.
  4. Litigation associated with their neck and/or upper limb pain.
  5. Insufficient English language skills to complete the questionnaires and follow-up instructions.
  6. Inability to complete the treatment and follow-up schedule.
  7. Current pregnancy.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

23 participants in 2 patient groups

Therapeutic Ultrasound
Active Comparator group
Description:
Therapeutic ultrasound applied for a period of 5 minutes to the most painful region of the neck, then a second 5 minute dose at the most painful region of the upper extremity
Treatment:
Device: Therapeutic Ultrasound
Soft Tissue Mobilization
Experimental group
Description:
Passive soft tissue mobilization to the neck and upper extremity
Treatment:
Other: Soft Tissue Mobilization

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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