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NCT06271720 Clinical Trial

Impact of Visceral Manipulation Versus Integrated Neuromuscular Inhibition Technique in Shoulder Impingement Syndrome

Shoulder Impingement Clinical Trial

Official title:
Impact of Visceral Manipulation Versus Integrated Neuromuscular Inhibition Technique in Shoulder Impingement Syndrome

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06271720
Other study ID # faculty of physical therapy
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 2024
Est. completion date May 2024

Study information
Verified date February 2024
Source Egyptian Chinese University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will be conducted To evaluate the effect of Visceral Manipulation versus Integrated Neuromuscular Inhibition Technique on the upper fiber of trapezius on pain intensity, pain threshold, shoulder range of motion, and function in shoulder impingement syndrome

Description:

HYPOTHESES It will be hypothesized that: 1. There will be no statistically significant effect of Visceral Manipulation on the upper fiber of the trapezius on pain intensity, pain threshold, shoulder range of motion, or function in shoulder impingement syndrome 2. There will be no statistically significant effect of the Integrated Neuromuscular Inhibition Technique on the upper fiber of the trapezius on pain intensity, pain threshold, shoulder range of motion, or function in shoulder impingement syndrome. 3. There will be no statistically significant difference in the effect of visceral manipulation versus the integrated neuromuscular inhibition technique on the upper fiber of the trapezius on pain intensity, pain threshold, shoulder range of motion, and function in shoulder impingement syndrome. This study will be conducted to answer the following questions: Is there an effect of Visceral Manipulation versus Integrated Neuromuscular Inhibition Technique on the upper fiber of the trapezius on pain intensity, pain threshold, shoulder range of motion, and function in shoulder impingement syndrome?

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 75
Est. completion date May 2024
Est. primary completion date May 2024
Accepts healthy volunteers No
Gender All
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - -active myofascial trigger points in the upper trapezius muscle, and chronic Pain lasting more than 12 weeks - BMI between 25 and 30 Kg/m². Exclusion Criteria: - a previous fracture in the cervical spine or shoulder surgery - acute inflammatory condition. - Malignant tumor. - Multiple osteophytes. - Cervical posture abnormalities. - Osteoporosis.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• visceral manipulation
visceral manipulation: A palpation technique will be applied till the barrier is felt and it will be applied until release is felt. integrated neuromuscular inhibition: ischemic compression will be applied to trigger point of upper trapezius
• integrated neuromuscular inhibition
It involves applying direct sustained digital pressure to the TrP with sufficient force over dedicated time duration, to slow down the blood supply and relieve the tension within the involved muscle. The pressure is gradually applied, maintained and the gradually released

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Noha Elserty

Outcome
Type Measure Description Time frame Safety issue
Primary pain intensity pain intensity will be measured by a visual analog scale, the scale is marked from 0 to 10 while 0 represents no pain and 10 represents intolerable pain pre treatment and after 4 weeks
Primary pain pressure threshold pressure threshold measured by pressure algometer pre treatment and after 4 weeks
Primary shoulder range of motion shoulder flexion and abduction range of motion will be measured by inclinometer pre treatment and after 4 weeks
Primary shoulder functional level The functional level of the shoulder will be measured by shoulder pain and disability index. the index consists of subscales that measure how much shoulder pain interferes with the functional activity of daily living pre treatment and after 4 weeks
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