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NCT07313189Completed

Stabilizer Pressure Biofeedback on Neck Dysfunction

Effect of Stabilizer Pressure Biofeedback on Neck Dysfunction Post Neck Dissection Surgeries

Source: ClinicalTrials.gov · Last updated 5 Jan 2026

Brief summary (registry, in English)

Fifty patients of both genders with age ranged from 30 - 50 years, suffering from neck dysfunction post neck dissection surgeries participated in this study. The participants were randomly selected from the National Cancer Institute, Cairo, Egypt. They were randomly assigned into two equal groups, 25 patients each (study group and control group). Group A :( Study Group) In this group of the study, received cranio-cervical flexion training utilizing stabilizer pressure biofeedback in addition to traditional physical therapy program (ROM exercises, stretching and strengthening exercises), 3 times a week for 6 weeks. Group B :( Control Group) In this group of the study, received traditional physical therapy program (ROM exercises, stretching and strengthening exercises), 3 times a week for 6 weeks.

Status (registry)
Completed
Study type
Interventional
Enrollment
50 (actual)
First submitted
17 Dec 2025
Start date
10 Sept 2025
Primary completion date
20 Nov 2025
Lead sponsor
Cairo University
NCT number
NCT07313189

What you commit to

  • Study type: Interventional
  • Participants enrolled: 50
  • From 10 Sept 2025 to the primary completion date, 20 Nov 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • 1- Neck pain due to other underlying conditions such as:
    • Spinal fracture
    • Osteoporosis
    • Spinal cord compression
    • Congenital postural deformities
    • Inflammatory disorders of the spine
    • Spinal infections
    • Significant neurological disorders
    • Rheumatoid arthritis 2- Malignancy 3- Pregnancy 4- History of cervical spine surgery 5- Epilepsy or any psychological disorders

Who the study is looking for

  • The subject selection was according to the following criteria:
    • Patients' age ranged between 30-50 years.
    • Both gender participated in this study.
    • All patients suffered from neck dysfunction (neck pain, limited ROM and disability) following unilateral neck dissection surgeries.
    • All patients suffered from moderate to severe pain (VAS score \> 4).
    • All patients undergone modified radical NDS or selective NDS.
    • All patients began the treatment program 2 weeks post neck dissection surgeries
    • All patients enrolled to the study had their informed consent.

Age in the registry: 30 years to 50 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Faculty of Physical Therapy
Coordinator of this site? Confirm its status
GizaEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.