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Influence of Extracorporeal Shockwave Therapy in Patients of Mechanical Neck Pain

B

Benha University

Status

Completed

Conditions

Mechanical Neck Pain
Pain Threshold
Extracorporeal Shock Wave Therapy
Cervical Pain, Posterior
Neck Pain
Neck Pain Musculoskeletal

Treatments

Device: Extracorporeal Shockwave therapy
Other: Exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT07266272
Shockwave in neck pain

Details and patient eligibility

About

Purpose:

The study aimed to determine whether adding extracorporeal shockwave therapy (ESWT) to a standardized physiotherapy program provides additional benefits for patients with chronic mechanical neck pain. Specifically, it examined effects on pain intensity, pressure pain threshold (PPT), neck disability index (NDI), cervical active range of motion (AROM), and joint position sense (JPS).

Full description

Study Summary Summary of the Study: Influence of Extracorporeal Shockwave Therapy in Patients with Mechanical Neck Pain

Purpose:

The study aimed to determine whether adding extracorporeal shockwave therapy (ESWT) to a standardized physiotherapy program provides additional benefits for patients with chronic mechanical neck pain. Specifically, it examined effects on pain intensity, pressure pain threshold (PPT), neck disability index (NDI), cervical active range of motion (AROM), and joint position sense (JPS).

Key Details:

  • Study Design: Double-blinded, pretest-posttest controlled clinical trial.

  • Participants: 52 patients aged 18-29 with chronic mechanical neck pain for over 3 months.

  • Groups:

    • Group A: Standardized physiotherapy only (stretching, isometric exercises, posture training).
    • Group B: ESWT + standardized physiotherapy.
  • Duration: 4 weeks, 2 sessions/week (1 ESWT + 1 physiotherapy in Group B).

  • Assessments: NPRS for pain, pressure algometer for PPT, Arabic NDI, goniometer for AROM & JPS.

  • Results:

    • Adding ESWT significantly improved PPT, left cervical rotation AROM, cervical extension JPS, and right cervical rotation JPS.
    • No significant differences between groups in other measures.
  • Conclusion: ESWT combined with physiotherapy may enhance pain threshold, AROM in rotation, and proprioception compared to physiotherapy alone.

Sources of Strength in the Study:

  1. Double-blind design reduces bias.
  2. Randomized allocation with adequate sample size determined by power analysis.
  3. Use of validated measurement tools (NPRS, NDI Arabic version, Wagner algometer, standard goniometer).
  4. Clearly defined inclusion/exclusion criteria ensuring sample homogeneity.
  5. Use of standardized physiotherapy protocol enhances reproducibility.

Enrollment

52 patients

Sex

All

Ages

18 to 29 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. The patients (both males and females) with chronic non-specific neck pain for more than three months.
  2. The patient's age is between 18 and 29 years old.
  3. The patient has at least one taut band at the upper fibers of the trapezius as described in assessment procedures.
  4. patient's numeric pain rating scale (NPRS) was 3 to 8 out of 10

Exclusion criteria

  1. Were treated for neck or shoulder pain during the last three months.
  2. Had a neck or shoulder operation during the last two years.
  3. Had any structural pathology of the cervical spine, such as disk prolapse, spinal stenosis, or cervical spondylosis.
  4. Had a traumatic history, instability, and spasmodic torticollis.
  5. Had cardiovascular, respiratory, or allergic disease or neck osteoarthritis.
  6. Had homeostatic disorders.
  7. Fibromyalgia, shoulder diseases (tendonitis, bursitis, capsulitis).
  8. Inflammatory rheumatic diseases.
  9. Severe psychiatric illness and other diseases that restrict physical loading, and pregnancy (Salo et al., 2010).
  10. Patients with vertebrobasilar insufficiency and vertigo.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

52 participants in 2 patient groups

Control group, standardized physiotherapy group receiving (Stretch, strength, Postural correction)
Other group
Description:
The control group recieve conventional program without additional shockwave
Treatment:
Other: Exercise
Intervention group received Extracorporeal shockwave therapy + Standardized physiotherapy as control
Experimental group
Description:
Group B
Treatment:
Other: Exercise
Device: Extracorporeal Shockwave therapy

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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