Effects of posterior oblique sling strengthening on Temporo-Spatial gait parameters in young adults

NCT ID NCT06944769

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First seen Sep 10, 2026 ยท Last updated Sep 10, 2026

Summary

The aim of this study is to determine the effects of posterior oblique sling strengthening on gait parameters (speed, stride length, and cadence), gluteus maximus strength, latissimus dorsi flexibility, and trunk rotation in young adults. A randomized clinical trial will be conducted at Riphah Internal university, Rawal General \& Dental Hospital and Rawal Institute of Rehabilitation \& Health Sciences. Recruiting 48 participants aged 18-30 years with unilateral or bilateral posterior oblique sling tightness. Participants will be randomly assigned into two groups through the sealed envelope method. The intervention will be performed four times per week for three weeks, followed by a home-based program from weeks 4 to 6. Assessments will be conducted at baseline, post-1st session, weekly during intervention, and at week 6. Tools used include Inclinometer (for lumbar range of motion), Goniometer (to assess latissimus dorsi length), Waistband Pedometer (to measure gait parameters such as cadence, walking speed, and stride length), Hand-held Dynamometer (to assess gluteus maximus strength), Inches Tape (for Pectoralis Minor Length Test to evaluate muscle flexibility and scapular positioning) and demographic measures..

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Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

46 people

The number who actually took part.

Started

Apr 2025

Finished

Feb 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 30 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age 18-30 years. * Both Genders: Male and Female. * Participants either unilateral or bilateral POS tightness. * Participants had latissimus dorsi tightness indicates: * Modified rotation test (10-degree rotation difference than contralateral side) * Participants had gluteal maximus weakness indicates: * Prone hip extension test (unable to lift leg more than 15 degrees or do compensatory mechanism) Exclusion Criteria: * Participants who have pectoralis minor tightness indicates: * Pectoralis Minor Length Test (assessing the ability to flatten the posterior shoulder with posterior force applied in a supine position distance greater than 2.6 cm (1 inch) by inches tape indicate Pectoralis Minor tightness). * Diagnosed Lumbar spondylosis. * Diagnosed disc prolapse. * Diagnosed neurological deficits. * Diagnosed cerebellar or vestibular lesions impacting balance and gait. * The presence of knee, ankle, or hip pathologies that impair lower limb function. * Spine surgery within the past 12 months * Unable to understand and follow the commands

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As listed by the trial registrant

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Contacts and locations

Locations

  • Rawal Institute of Rehabilitation & Health Sciences (RIRH) & Rawal General & Dental Hospital. (RG&DH)

    Islamabad, Capital, 45550, Pakistan

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