NCT06613607

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.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jun 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2024

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

September 23, 2024

Completed
3 days until next milestone

First Posted

Study publicly available on registry

September 26, 2024

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2025

Completed
29 days until next milestone

Study Completion

Last participant's last visit for all outcomes

January 30, 2025

Completed
Last Updated

September 26, 2024

Status Verified

August 1, 2024

Enrollment Period

7 months

First QC Date

September 23, 2024

Last Update Submit

September 23, 2024

Conditions

Outcome Measures

Primary Outcomes (3)

  • Lumber lordotic angle

    Lumber 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.

    6 weeks

  • Dynamic Balance

    Measured 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.

    6 weeks

  • Agility

    It 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.

    6 weeks

Study Arms (1)

Experimental group

EXPERIMENTAL

The group will receive strengthening treatment protocol. Strengthening will be divided into following phases 1. Warm up phase: 2. Strengthening phase: 3. Cool down phase:

Other: Core Strengthening

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

Experimental group

Eligibility Criteria

Age19 Years - 35 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Foundation University College of Physical Therapy

Rawalpindi, Punjab Province, 46000, Pakistan

RECRUITING

Central Study Contacts

Hafsa Irfan, MS-MSKPT*

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: Quasi Experimental Study
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 23, 2024

First Posted

September 26, 2024

Study Start

June 1, 2024

Primary Completion

January 1, 2025

Study Completion

January 30, 2025

Last Updated

September 26, 2024

Record last verified: 2024-08

Locations