Actively Recruiting

Phase Not Applicable
Age: 19Years - 35Years
All Genders
NCT06613607

Effects of Core Strengthening on Pelvic Tilt, Dynamic Balance and Agility in Lower Cross Syndrome: a Quasi-experimental Study

Led by Foundation University Islamabad · Updated on 2024-09-26

20

Participants Needed

1

Research Sites

34 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is a quasi experimental study and the purpose of this study is to determine the effects of core strengthening on pelvic tilt, dynamic balance and agilty in lower cross syndrome.

CONDITIONS

Official Title

Effects of Core Strengthening on Pelvic Tilt, Dynamic Balance and Agility in Lower Cross Syndrome: a Quasi-experimental Study

Who Can Participate

Age: 19Years - 35Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 19-35 years
  • Both genders
  • Positive modified Thomas test
  • Positive prone hip extension strength test
  • Positive trunk flexion strength test
  • Tight erector spinae
  • Asia Pacific 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 position
Not Eligible

You will not qualify if you...

  • Acute flare of low back pain
  • Centralization and peripheralization of pain
  • Signs of stenosis (leg symptoms when walking eased upon flexion)
  • Pain due to repetitive movements
  • Paresthesia or numbness
  • Structural deformity (kyphosis, spondylosis, spondylolisthesis, scoliosis, and joint contractures)
  • Curve reversal
  • Pregnancy
  • Post surgery
  • Degenerative and inflammatory spine diseases

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Foundation University College of Physical Therapy

Rawalpindi, Punjab Province, Pakistan, 46000

Actively Recruiting

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Research Team

H

Hafsa Irfan, MS-MSKPT*

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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