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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06613607
Enrollment
20
Registered
2024-09-26
Start date
2024-06-01
Completion date
2025-01-30
Last updated
2024-09-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lower Cross Syndrome

Brief summary

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.

Detailed description

Participants will be recruited into the study using the criteria of lower crossed syndrome which is assessed using te following tests: Prone hip extension test Trunk flexion strength test Tightness in erector spinae Modified Thomas test

Interventions

Strengthening protocol will comprise of following three phases: Warm up phase Following exercise would be performed in warm up; Scissor skier, Criss cross crunches, , Hip circles, Bent over twist. Strengthening: Abdominal bracing Bracing with heel slides Bracing with leg lifts Bracing with bridging Quadruped alternate arm and leg lifts with bracing Side support with knees flexed Cool down phase: Following exercise would be performed for cood down: Child's pose, Cat cow stretch, Lower back stretch, Obliques stretch

Sponsors

Foundation University Islamabad
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Quasi Experimental Study

Eligibility

Sex/Gender
ALL
Age
19 Years to 35 Years
Healthy volunteers
No

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 * 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 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

Design outcomes

Primary

MeasureTime frameDescription
Lumber lordotic angle6 weeksLumber lordotic angle will be measured using a mobile applicationOne sensor will be placed at T12- L1 and other sensor will be placed at L5- S1. The sum of these two angles will be calculated.
Dynamic Balance6 weeksMeasured using the star excursion test. It is performed with the subject standing on the middle of the grid on the leg to be tested. The grid consists of 8 lines corresponding to the direction of reach extending out from the center at 45 degrees. The subject will try to reach as far as possible with their feet and the distance from the center will be measured and recorded. This will be repeated 3 times for that direction and performed so for all the directions.
Agility6 weeksIt will be measured using the Illinois agility test, The subject will lie on their front (head to the start line). On the 'Go' command the stopwatch is started, and the subject gets up as quickly as possible and runs forwards 10 meters to run around a cone, then back 10 meters, then runs up and back through a course of four cones. Finally, the athlete runs another 10 meters up and back past the finishing cone, at which the timing is stopped.

Countries

Pakistan

Contacts

Primary ContactHafsa Irfan, MS-MSKPT*
hafsairfan198@gmail.com03325312241

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026