Additional Effects of Surface Electromyographic Biofeedback on Post Facilitation Stretching and Strengthening in Lower Crossed Syndrome;A Randomized Control Trial

Not Applicable

Recruiting

• Conditions: Lower Cross Syndrome

• Registration Number: NCT06613620
• Lead Sponsor: Foundation University Islamabad

Brief Summary

This study is a randomised control trial and the purpose of this study is to determine the additional effects of surface electromyographic biofeedback on post facilitation stretching and strengthening in lower crossed syndrome.

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Detailed Description

Participants will be recruited into their respective groups using a coin toss method. Lower crossed syndrome will be assessed using the following tests:

Prone hip extension test Trunk flexion strength test Tightness in erector spinae Modified Thomas test

Study Timeline

• Study Start: 2024-07-18
• Status Verified: 2024-09
• Study First Submitted: 2024-09-23
• Study First Submitted QC: 2024-09-23
• Last Update Submitted: 2024-09-23
• Study First Posted: 2024-09-26
• Last Update Posted: 2024-09-26
• Primary Completion: 2025-06-02
• Study Completion: 2025-06-20

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 42

Inclusion Criteria

• Age 19-35 years
• Both genders
• Positive modified Thomas test
• Positive prone hip extension strength test
• Positive trunk flexion strength test
• Tight erector spinae
• BMI normal (18.5-24.9 Kg/m2)
• Local intermittent lumbar pain
• moderate pain (NPRS 3-7)
• Painless movement and activity
• Pain only produced by sustained loading in relevant position, which is then relieved on moving from that pos

Exclusion criteria:

• Acute flare of LBP
• Centralization and peripheralization of pain
• Signs of stenosis(leg symptoms when walking that are eased upon flexion)
• Pain due to repetitive movements
• Paresthesia/Numbness
• Structual deformity(Kyphosis, spondylosis, spondylolisthesis,scoliosis and joint contractures)
• Curve reversal
• Pregnancy
• Post surgery
• Degenerative and inflammatory spine diseases

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Lumber lordotic angle	4 weeks	It will be measured using a mobile application. One sensor will be placed at the T12-L1 and other at L5-S1 spinous processes. The two angles will be recorded and their sum will be considered as the lumber lordotic angle.
Joint position sense	4 weeks	One sensor will be placed at T12-L1 and the other placed at L5-S1 simultaneously. Patient will be asked to flex and then extend maximally; his end ranges will be recorded. Within the middle range, therapist will decide the targeted angle for individualized patient. Patient will be asked to memorize the target position for 5seconds. The absolute error will measure by subtracting the actual angle and the target angle.
pain intensity	4 weeks	It will be measured on a numeric pain rating scale in which the subjects select a number ranging from 0-10 according to their intensity of pain. '0' score indicates no pain while '10' indicates worst pain experienced.
Functional disability	4 Weeks	It will be measured using a Modified Oswestry lower back Disability Index. It is a 10item based questionnaire and each item is further divided into 6statements. The score of '0-4' indicated no disability while 35-50 indicate complete disability.

Trial Locations

Locations (1)

Foundation University College of Physical Therapy; 🇵🇰 Punjāb Chak, Punjab, Pakistan