Effects Of Posterior Oblique Sling Strengthening on Temporo-Spatial Gait Parameters in Young Adults
1 other identifier
interventional
46
1 country
1
Brief 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..
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2025
1 active site
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
January 7, 2025
CompletedFirst Submitted
Initial submission to the registry
February 20, 2025
CompletedFirst Posted
Study publicly available on registry
April 25, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
January 31, 2026
CompletedApril 25, 2025
April 1, 2025
12 months
February 20, 2025
April 17, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Hand-held dynamometer for gluteal maximus strength:
The hand-held dynamometer is used to assess gluteus maximus strength by measuring the force exerted during hip extension. The patient is positioned in the prone position with the knee flexed at 90°, and the dynamometer is placed just above the knee on the posterior side of the leg. The patient then extends the hip against the resistance provided by the dynamometer, with measurements recorded in kilograms or pounds. The test is repeated 2-3 times to ensure consistency, with adequate rest between repetitions.
Baseline to 6 weeks
Waist band Pedometer:
The waistband pedometer is used to measure gait parameters the pedometer records the total steps taken over a set time, which is divided by time to calculate steps per minute.
Baseline to 6 weeks
Secondary Outcomes (8)
Goniometer ( Latissimus Dorsi length)
Baseline to 6 weeks
Inches Tape (for Pectoralis Minor length Test)
Baseline to 6 weeks
Inclinometer for lumbar flexion
Baseline to 6 weeks
Inclinometer for lumbar extension
Baseline to 6 weeks
Inclinometer for lumbar right lateral flexion
Baseline to 6 weeks
- +3 more secondary outcomes
Study Arms (2)
Group A Myofascial technique
ACTIVE COMPARATORGroup A follows a six-week, five-day-per-week protocol (30-40 min) targeting posterior oblique sling activation.
group B (posterior oblique sling strengthening protocol)
EXPERIMENTALA six-week conservative protocol, conducted five times per week for 30-40 minutes, focusing on core stability exercises.
Interventions
Group A with MET (latissimus dorsi), myofascial release (thoracolumbar fascia) and posterior oblique sling strengthening it will be a six-week protocol, with sessions conducted five times a week for 30-40 minutes, focusing on posterior oblique sling activation. Week 1: Myofascial release (thoracolumbar fascia, 60-90 sec), MET (latissimus dorsi, 7-10 sec isometric + 30-sec stretch, 5 reps), glute max strengthening (prone hip extensions, 10-sec holds ×5; bilateral bridges, 5-sec holds ×5). Week 2: Prone hip extension (3-kg resistance), arm extension (1-kg dumbbell, 5-sec holds ×5), bird-dog (5-sec holds ×10, 1 set). Weeks 3-4: Prone hip extensions (5-sec holds ×10), single-leg bridges (5-sec holds ×10), twice daily. Weeks 5-6: Increased intensity to 10-sec holds ×10 reps
A six-week conservative protocol, was conducted five times weekly for 30-40 minutes, focuses on core stability exercises. Week 1 includes static stretching of the latissimus dorsi (30-second hold, 3 reps) and prone hip extensions with knee flexed at 90° (5-second hold, 10 reps). By Week 2, bird-dog exercises are introduced (5-second hold, 10 reps per side). In Weeks 3-6, these exercises are maintained to provide a stable baseline for comparison with Group A's more intensive protocol. The latissimus dorsi stretch is performed 2-3 times daily for improved flexibility.
Eligibility Criteria
You may qualify if:
- 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)
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Rawal Institute of Rehabilitation & Health Sciences (RIRH) & Rawal General & Dental Hospital. (RG&DH)
Islamabad, Capital, 45550, Pakistan
Study Officials
- PRINCIPAL INVESTIGATOR
Aisha Razzaq, PHD*
Riphah International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 20, 2025
First Posted
April 25, 2025
Study Start
January 7, 2025
Primary Completion
December 30, 2025
Study Completion
January 31, 2026
Last Updated
April 25, 2025
Record last verified: 2025-04
Data Sharing
- IPD Sharing
- Will not share