- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07578935
Comparative Effects of Dynamic Stability Drills and Plyometric Training After Anterior Crutiate Ligament Reconstruction
May 5, 2026 updated by: Riphah International University
Comparative Effects of Dynamic Stability Drills and Plyometric Training on Terminal Extension Lag After Anterior Cruciate Ligament Reconstruction
Terminal Extension lag (TEL) is a condition that develops when active range of extension is smaller than passive range; frequently noticed in post-traumatic knees after injuries and Anterior Cruciate ligament reconstruction surgery.
TEL is typically seen within 6 to 12 weeks after ACL reconstruction.
Anterior cruciate ligament reconstruction surgery is a critical surgical intervention used to repair ACL tear; which is common among those who are engaged in physical demanding activities and Sportsmen.
In the initial days following surgery terminal extension lag affects up to 10 to 35% of individuals.
ACL is expectational because it's not just a static stabilizer of knee but also transfers proprioceptive information to the brain so to improve joint's dynamics.
This study aims to compare effects of Dynamic Stability Drills (DSD) and Plyometric Training (PT) in reducing terminal knee extension lag in post-ACL reconstruction patients.
This study will be a Randomized Clinical Trail and will be conducted in Physiotherapy Department of Bethania Hospital Sialkot.
Non-Probability Convenience Sampling will be used to collect data.
Total of 48 Participants of the age 20 to 40 years with terminal extension lag of moderate lag stage (typically 9-12 weeks post-op with 5-10° lag) will be selected as sample size.
An informed consent will be taken prior study from all the subjects.
Outcomes measure will be included Numerical Pain Rating Scale (NPRS) for pain, Single Leg Hope Test and Y Balance Test (Y-BAL) for Dynamic Stability, Universal Goniometer (UG) for Range of Motion, Sphygmomanometer for Knee Strength, International Knee Documentation Committee scores, (IKDC) for Knee function and Limb Symmetry Index (LSI) Calculations.
Subjects will be divided into two groups by random number generator table.
Both groups will receive a standard physiotherapy protocols which will include: Hot pack , TENS , Mobilizations, Stretching and Strengthening.
Group A will receive Dynamic Stability Drills and Group B will receive Plyometric Training along with conventional treatment.
Patient will come 3 time a week and data will be recollected after 6 weeks.
Data will be analyzed by SPSS version 25.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
48
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Rabiya Noor, PhD
- Phone Number: 0334 4355660
- Email: rabiya.noor@riphah.edu.pk
Study Locations
-
-
Punjab Province
-
Lahore, Punjab Province, Pakistan, 54000
- Recruiting
- Rabiya Noor
-
Contact:
- iqbal Tariq, phd
- Phone Number: 03338236752
- Email: iqbal.tariq@riphah.edu.pk
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Age 20-40
- Both Genders (male & female)
- History of Anterior Cruciate Ligament Reconstruction (ACLR) between 1-3 years
- Moderate stage (5 to 10 ˚) of terminal extension lag after ACL reconstruction
Exclusion Criteria:
- Any other previously serious knee pain and/or surgery limiting of knee range of motion(2)
- Any traumatic conditions around the knee, or any infectious or tumors conditions i.e.
meniscus injury, fracture, dislocation or osteochondral injury
- Pregnancy, any recently underwent abdominal and back surgery
- BMI ≥ 30 kg/m²
- Any systemic and/or neurological illness, rheumatoid arthritis, osteomyelitis, any neurological disorders, spinal disorders, obesity, Dementia, inflammatory conditions like Ankylosing spondylitis, Rheumatoid arthritis, Osteoporosis, Diabetic neuropathy,
- Red flags such as Trauma, Cancer, Constitutional Symptoms (Fever, Malaise, Weight Loss), Recent Infection, Mental retardation, Hemiparesis / Hemiplegia
- Subjects with presence of any fractures
- Heart/diabetic patients
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Plyometric Training
|
Weak 1-2: Four types of plyometrics: A) bilateral off-set (alternating box jump) B) bilateral asymmetrical (split jump) C) bilateral symmetrical (30 cm drop jump) and D) unilateral (30 cm drop jump(13) Weak 3-4:
|
|
Experimental: Dynamic Stability Drills
|
Weak 1-2 Stability Foundation Weight shifts (anterior/posterior, lateral, Double-leg stance on foam surface, Eyes-closed balance (double-leg), Isometric quad & hamstring contractions, Wall sits + small ball between knees (activate adductors & quads)Weeks 3-4: Progressive Dynamic Stability, Single-leg stance on foam, Thera-band perturbation drills (knees and hips), TKE (Terminal Knee Extension) on unstable surfaces, Step-downs from 6-inch height (with control),Lateral step-overs (slow & controlled)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Single leg hope test
Time Frame: 6th week
|
Jumping as far as you can on one leg while maintaining your balance and landing firmly is the goal of this challenge.
The starting line and the landing leg's heel are used to estimate the distance
|
6th week
|
|
Limb Symmetry Index (LSI) Calculation
Time Frame: 6th week
|
the Limb Symmetry Index (LSI) calculates the performance difference between two limbs, typically the affected and unaffected limbs following an accident; by dividing the score of the injured limb by the score of the unaffected limb and multiplying the result by 100.
It's represented in percentage
|
6th week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Rabiya Noor, PhD, Riphah International University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 15, 2026
Primary Completion (Estimated)
May 15, 2026
Study Completion (Estimated)
June 15, 2026
Study Registration Dates
First Submitted
May 5, 2026
First Submitted That Met QC Criteria
May 5, 2026
First Posted (Actual)
May 11, 2026
Study Record Updates
Last Update Posted (Actual)
May 11, 2026
Last Update Submitted That Met QC Criteria
May 5, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR&AHS/25/0148
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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