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

NCT ID
NCT07642752
Registry status
Recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
Riphah International University
Conditions
Anterior Cruciate Ligament Injuries

Overview

ClinicalTrials.gov lists this study as Recruiting.

Official title: Effects of Perturbation Training Versus Task-oriented Functional Activities on Pain, Range of Motion, Balance and Function in Post-anterior Cruciate Ligament Reconstruction

Enrollment: 54 participants (Estimated).

What is being studied

  • Other: Control Group (Standard Rehabilitation Protocol)
  • Intervention: Control Groups
  • Intervention: Epidemiologic Methods
  • Intervention: Epidemiologic Research Design
  • Intervention: Investigative Techniques
  • Intervention: Methods
  • Other: Perturbation Training Group
  • Intervention: Research Design
  • Other: Task-Oriented Functional Activities Group

Who may be eligible

Ages
18 Years to 45 Years
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

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: * 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

Study locations

1 study location is listed.

Recruiting site status is explicitly provided for 1 location; 1 is listed as Recruiting.

Countries: Pakistan

  • Punjab Province, Pakistan: 1

Sample of listed locations

  • Ghurki Hospital Lahore — Lahore, Punjab Province, 54000, Pakistan — Recruiting

Study details

Start date
August 1, 2026
Primary completion date
November 15, 2026
Completion date
November 26, 2026
First posted
June 11, 2026

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07642752
Registry last updated
September 24, 2026
QualifiedStudies registry data refreshed
October 5, 2026
QualifiedStudies record fetched
October 5, 2026

View NCT07642752 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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