ClinicalTrials.gg
RecruitingNCT07642752Updated Sep 24, 2026

Perturbation Training vs Functional Activities on Pain, ROM, Balance, and Function Post-ACL

An interventional study of Perturbation Training Group and Task-Oriented Functional Activities Group in Anterior Cruciate Ligament Injuries, sponsored by Riphah International University. Recruiting at 1 site in Pakistan. Open to participants aged 18 Years to 45 Years. Per ClinicalTrials.gov, last updated 2026-09-24.

Sponsored by Riphah International University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Aug 2026; still recruiting 3 months later.

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Phase
Not applicable
Study type
Interventional
Enrollment
54
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-15

Among 13 studies in Anterior Cruciate Ligament Injuries with a site in Pakistan — 2 open to participants now, 5 under way, none of them phase 3. Anterior Cruciate Ligament Injuries · Pakistan.

Planned enrollment
6th of 12
54 · median 52
Started
2026
with 2 others
No phase
12 of 13
2 open now
Registered
11th of 13
by date
Lead sponsor
6 of 13
Riphah International University

Among the 13 studies in Anterior Cruciate Ligament Injuries with a site in Pakistan, this one is the 6th largest by planned enrollment of the 12 interventional ones that give a count, is one of 3 that started in 2026, is one of 12 with no phase, and was the 11th registered.

Anterior Cruciate Ligament Injuries

625 studies on the registry are indexed under Anterior Cruciate Ligament Injuries; 192 are open to participants now.

Browse Anterior Cruciate Ligament Injuries studies →

Open to participants now

2 of the 13 studies in Anterior Cruciate Ligament Injuries with a site in Pakistan are open now. Recruiting first, the newest first:

All 2 open studies →

A study can be open while its sites in Pakistan have not opened yet or have stopped. Only those recruiting at a site in Pakistan →

Who these studies take

Of the 122 Anterior Cruciate Ligament Injuries studies recruiting now, 27 (22%) set no upper age limit and 92 (75%) stop at 75 or younger; 46 take children under 18; 21 take healthy volunteers.

This study: 18 Years to 45 Years · all sexes · no healthy volunteers.

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02

Study summary

Anterior cruciate ligament (ACL) injuries are among the most common and functionally disabling knee injuries, particularly in physically active individuals. Despite advancements in surgical techniques, optimal post-operative rehabilitation remains critical for successful functional recovery, minimizing re-injury risk, and restoring pre-injury performance levels

Read the detailed description

This randomized controlled trial aims to compare the effectiveness of perturbation training and task-oriented functional activities in patients following ACL reconstruction surgery. Perturbation training is a neuromuscular re-education strategy that involves controlled, unexpected movements to enhance joint stability and proprioceptive feedback. In contrast, task-oriented functional training focuses on restoring movement through activities that mimic daily or sports-related functional tasks.

This study will be a Randomized Control Trail and will be conducted in physiogic physiotherapy clinic and Ghurki Trust and Teaching Hospital. Non-Probability Convenient Sampling will be used to collect data. Total of 54 Participants of the age 18-45 years with post 12 weeks to 1 year ACL reconstruction will be included in the study. An informed consent will be taken prior study from all the subjects. Outcomes measure will be included Numerical Pain Rating Scale (NPRS) for pain, Universal Goniometer (UG) for Range of Motion, Y balance test for Knee Stability, International Knee Documentation Committee scores, (IKDC) for Knee function

03

Conditions studied

  • Anterior Cruciate Ligament Injuries

Keywords

  • Knee
  • Disability
  • Range of motion
  • Balance
04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age range: 18-45 years
  • Male participants only
  • History of Anterior Cruciate Ligament Reconstruction (ACLR) of 3 to 12 months
  • No prior ACL surgery on the affected knee
  • ACL reconstruction with autograft of hamstrings tendon
  • Knee flexion range of motion less than 120°
  • Extension lag less than or equal to 10°
  • Pain during functional activities

Exclusion criteria

Exclusion Criteria:

  • Any type of fracture
  • Concurrent ligamentous injury or repairable meniscus
  • Osteochondral defect
  • Any systemic and/or neurological illness
  • Rheumatoid arthritis
  • Osteomyelitis or any neurological disorders
  • Spinal disorders
  • Inflammatory conditions such as ankylosing spondylitis
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
54 participants (estimated)

Study arms

  • Experimental
    Perturbation Training Group

    Participants undergo perturbation-based exercises designed to improve knee stability. It includes balance boards, BOSU balls, and manual perturbation techniques.

    Other: Perturbation Training Group · Other: Control Group (Standard Rehabilitation Protocol)

  • Active comparator
    Task-Oriented Functional Activities Group

    Participants engage in functional movement exercises that mimic daily activities. It includes step training, agility drills, and controlled landing mechanics.

    Other: Task-Oriented Functional Activities Group · Other: Control Group (Standard Rehabilitation Protocol)

  • Sham comparator
    Control Group (Standard Rehabilitation Protocol)

    Participants follow traditional ACL rehabilitation without perturbation or task-oriented interventions. It includes strength training, range-of-motion exercises, and proprioceptive drills.

    Other: Control Group (Standard Rehabilitation Protocol)

Interventions

  • OtherPerturbation Training Group

    Two-leg rocker board One-leg rocker board Roller board / stable (weight scale) surface Roller board / BOSU ball TheraBand feedback / perturbation training Simple sport-specific technique on rocker board Moderate demand sport-specific technique on rocker board Advanced sport-specific technique on rocker board This sequence reflects a progressive challenge to knee stability, beginning with bilateral balance tasks, advancing to unilateral control, and culminating in sport-specific perturbation drills.

  • OtherTask-Oriented Functional Activities Group

    Functional Recovery Tasks After ACLR Normal walking gait Bilateral squat Unilateral foundation exercises - Single leg squat Bilateral landing Running - Run on treadmill Bilateral plyometric - Bilateral drop jump Unilateral landing / deceleration - Single leg deceleration Unilateral plyometric - Single leg drop jump Change of direction ability / coordination - 90º cut maneuver Sport-specific movements - Movement control under sport-specific change of direction This sequence reflects a progressive load and skill development pathway, starting from basic gait and bilateral tasks, moving toward unilateral control, plyometrics, and finally sport-specific agility.

  • OtherControl Group (Standard Rehabilitation Protocol)

    Heating pad (5-10 minutes) TENS (short bursts, 10-15 minutes, frequency 100 Hz) Stationary cycling Gentle range of motion exercises Passive and active-assisted ROM Isometric quadriceps contractions Straight leg raises Quadriceps setting with a towel under the knee Closed-chain exercises (e.g., wall sits, mini-squats) Hamstring curls Double-leg stance on foam pad This set emphasizes pain relief, mobility restoration, and foundational strength before progressing to advanced neuromuscular or sport-specific tasks.

06

What researchers measure

Primary outcomes

  1. NPRS for Pain

    Numeric Pain Rating Scale (NPRS) it is a unidimensional scale to measure pain intensity, particularly in adults. It is a 10-rating scale and an 11-point numeric scale in the form of a horizontal bar or line

    Time frame: 6 weeks

  2. Universal Goniometer for Range of motion

    A universal goniometer (UG) will be used to determine the range of motion of the target joint.

    Time frame: 6 weeks

  3. The Y-Balance test (YBT)

    The Y-Balance test (YBT) is used to assess dynamic balance impairments associated with lower extremity injuries such as ACL injury, patellofemoral pain syndrome, and ankle instability.

    Time frame: 6 weeks

  4. International Knee Documentation Committee scores (IKDC)

    Patients' knee function is evaluated using the International Knee Documentation Committee's (IKDC) Subjective Knee Form. Through 18 questions, it assesses symptoms, athletic activity, and general knee function; higher scores indicate better knee function.

    Time frame: 6 weeks

07

Study locations

1 of 1 sites recruiting
  • Ghurki Hospital Lahore
    Lahore, Punjab Province 54000, Pakistan
    Recruiting
    • Muhammad Musab, MSOMPT · Principal investigator
08

References and documents

Publications

  • Carter HM, Littlewood C, Webster KE, Smith BE. The effectiveness of preoperative rehabilitation programmes on postoperative outcomes following anterior cruciate ligament (ACL) reconstruction: a systematic review. BMC Musculoskelet Disord. 2020 Oct 3;21(1):647. doi: 10.1186/s12891-020-03676-6. PubMed 33010802 ↗
  • Hetsroni I, Mann G, Arami E, van Stee M, Marom N, Ohana N. Young men undergoing anterior cruciate ligament reconstruction with patellar tendon autograft and anteromedial drilling outperform at 5- to 10-year follow-up in terms of graft stability and activity levels compared to those undergoing reconstruction with hamstring autograft and transtibial drilling. J ISAKOS. 2024 Aug;9(4):540-548. doi: 10.1016/j.jisako.2024.04.001. Epub 2024 Apr 3. PubMed 38580054 ↗
  • Nawasreh Z, Logerstedt D, Marmon A, Snyder-Mackler L. Clinical and Biomechanical Efficacies of Mechanical Perturbation Training After Anterior Cruciate Ligament Rupture. J Sport Rehabil. 2019 Nov 1;28(8):877-886. doi: 10.1123/jsr.2017-0363. PubMed 30300071 ↗
  • Brown SR, Washabaugh EP, Dutt-Mazumder A, Wojtys EM, Palmieri-Smith RM, Krishnan C. Functional Resistance Training to Improve Knee Strength and Function After Acute Anterior Cruciate Ligament Reconstruction: A Case Study. Sports Health. 2021 Mar;13(2):136-144. doi: 10.1177/1941738120955184. Epub 2020 Dec 18. PubMed 33337984 ↗

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Aug 2026 (actual). Primary completion is estimated for Nov 2026, 3 months after the start.

Of 278 non-industry interventional studies with no phase under Anterior Cruciate Ligament Injuries, half reached primary completion within 31 months of starting (the median), counting those still running; a quarter within 14 and three quarters within 70. This study's planned 3 months is below that.

Counting every sponsor, half of 287 studies reached it within 30 months; a quarter within 14 and three quarters within 70.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 8, 2026
First posted
Jun 11, 2026
StartActual
Aug 1, 2026
Primary completionEst.
Nov 15, 2026
CompletionEst.
Nov 26, 2026
Last update
Sep 24, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07642752
Responsible party
Sponsor
First posted
Jun 11, 2026
Start date
Aug 1, 2026
Primary completion
Nov 15, 2026 (estimated)
Completion
Nov 26, 2026 (estimated)
Last update
Sep 24, 2026

Study contacts

Imran Amjad, PhD
Contact
Imran.amjad@riphah.edu.pk
03324390125
Hira Butt
Contact
hirabutt7582@gmail.com
03360405480
Hira Shaukat, Mphill
principal investigator · Riphah International University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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