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Chitosan Phonophresis on Cervical IN Smartphone Addicted Users

Not Applicable
Recruiting
Conditions
Cervical Pain
Interventions
Drug: Chitosan Phonophresis
Other: selected physical therapy exercise
Registration Number
NCT06491992
Lead Sponsor
October 6 University
Brief Summary

A phonophoresis-based drug delivery system is a synchronous approach to improve local drug penetration in neuromuscular diseases associated with neuronal damage, excruciating pain, and local inflammation. Chitosan, a semi-synthetic material, is obtained by partial deacetylation of chitin amines, resulting in copolymers of N-acetylglucosamine and N-glucosamine. Its use has been explored in various biomaterial and medical applications. Chitosan has emerged as a cost-effective, biocompatible, and biodegradable material with many desirable biological properties, improvement of homeostasis and antiviral potential. Chitosan was found to suppress pro-inflammatory cytokines and decreased peripheral nerve edema, the polycationic nature of chitosan allows it to absorb protons, which reduces inflammation and provides an analgesic effect.

Detailed Description

The patients will randomly be divided into two equal groups; the control group which will receive the selected exercise program and the study group will receive the same exercise training program in addition to Chitosan Phonophresis, three times per week for four weeks.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Their age will be ranged from 16-18 years
  • body mass index will be 26.58 kg/m2.
  • used a smart phone for more than 1 year for at least 2 hours per day
  • complaining of neck pain after using a smart phone, addiction to smart phone in accordance with the smart phone addiction scale (SAS)
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Exclusion Criteria
  • any previous head and neck injuries or surgeries
  • any congenital abnormalities or symptomatic deformity in either the cervical or the lumbar spine
  • any uncorrected visual or auditory problems, dizziness, vertigo and headache
  • any systematic diseases, any addiction to alcohol, any additive drugs and sedatives within 48 hours previous to tests
  • body mass index of subjects over25 kg/m2.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
study groupselected physical therapy exerciseChitosan Phonophresis intervention
study groupChitosan PhonophresisChitosan Phonophresis intervention
control groupselected physical therapy exercisethe selected exercise program
Primary Outcome Measures
NameTimeMethod
Smartphone Addiction Scale-Short Version (SAS-SV)four weeks

SAS-SV was psychometrically robust in measuring the severity of smartphone addiction

The visual analogue scalefour weeks

was utilized to evaluate pre- and post-treatment neck pain

Neck disability indexfour weeks

assess how neck pain and other symptoms manifested during various functional activities. Ndi had been reported as a reliable (Cronbach's alpha: 0.89) and valid instrument to evaluate self-rated disability in patients with neck pain

Secondary Outcome Measures
NameTimeMethod
Cervical ROMfour weeks

Cervical active ROM will be measured for each participant in the study by digital goniometer device.

Trial Locations

Locations (1)

Lama S Mahmoud

🇪🇬

Al JÄ«zah, Select State, Egypt

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