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Clinical Trials/NCT06320340
NCT06320340
Completed
N/A

The Effectiveness of Neuromuscular Electrical Stimulation Applied Simultaneously to Exercise on Pain, Range of Motion, Muscle Endurance, Fear of Movement and Disability in Chronic Neck Pain

Istanbul University - Cerrahpasa (IUC)1 site in 1 country36 target enrollmentMarch 15, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Chronic Neck Pain
Sponsor
Istanbul University - Cerrahpasa (IUC)
Enrollment
36
Locations
1
Primary Endpoint
Neck disability
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The aim of this randomized-controlled study was to determine the effectiveness of neuromuscular electrical stimulation (NMES) applied simultaneously to exercise on pain, static endurance of cervical deep flexor muscles, fear of movement and disability in chronic neck pain. The participants were randomly assigned to one group which in only five clinical pilates exercises were performed (Group I) or the other group which NMES was applied on lower trapezius and serratus anterior muscles while the same exercises were performing (Group II).

Detailed Description

The aim of randomized-controlled study was to determine the effectiveness of neuromuscular electrical stimulation (NMES) applied simultaneously to exercise on pain, static endurance of cervical deep flexor muscles, fear of movement and disability in chronic neck pain. This study, including adults with chronic neck pain aged between 18-65 years, was conducted in laboratory of xxx University from March 2021 to May 2021. The participants were randomly assigned to one group which in only five clinical pilates exercises were performed (Group I) or the other group which NMES was applied on lower trapezius and serratus anterior muscles while the same exercises were performing (Group II). Both groups received 20 minutes of treatment session two days a week for the 8 weeks. The pain intensity, range of motion (ROM), static endurance of cervical deep flexor muscles, fear of movement, and neck disability were assessed with Visual Analogue (VAS), universal goniometer, The Deep Neck Flexor (DNF) Endurance Test, Tampa Scale of Kinesiophobia (TSK) and Neck Disability Index (NDI), respectively. All the assessments were performed twice as before and end of the treatment.

Registry
clinicaltrials.gov
Start Date
March 15, 2021
End Date
September 15, 2021
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Istanbul University - Cerrahpasa (IUC)
Responsible Party
Principal Investigator
Principal Investigator

Aybike Senel

PT, MSc, Research Assistant, Principal Investigator

Istanbul University - Cerrahpasa (IUC)

Eligibility Criteria

Inclusion Criteria

  • (1) being aged from 18 to 65 years old,
  • (2) having neck pain shows mechanical nature longer than 3 months, and
  • (3) getting a score of at least 10 from Neck Disability Index.

Exclusion Criteria

  • (1) having a surgery on neck and shoulder regions,
  • (2) having a neurological symptom, and
  • (3) did not complete the process of the assessment and intervention of this study.

Outcomes

Primary Outcomes

Neck disability

Time Frame: at the end of the invervention program (8 weeks after from baseline)

The Neck Disability Index consisted 10 questions investigating the pain intensity and difficulty in lifting, reading, concentration, working, sleeping and recreational activities. Each question is scoring from 0 to 5 and higher score means greater disability.

Secondary Outcomes

  • Pain intensity(at the end of the invervention program (8 weeks after from baseline))
  • Range of Motion(at the end of the invervention program (8 weeks after from baseline))
  • Static endurance of cervical deep flexor muscles(at the end of the invervention program (8 weeks after from baseline))
  • Fear of the movement(at the end of the invervention program (8 weeks after from baseline))

Study Sites (1)

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