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Functional Outcomes of an Accelerated Rehabilitation Protocol for ACL Reconstruction in Amateur Athletes

Functional Outcomes of a Criterion-based Rehabilitation Protocol for Anterior Cruciate Ligament Reconstruction in Amateur Athletes: a Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05716529
Acronym
ACL
Enrollment
50
Registered
2023-02-08
Start date
2022-03-06
Completion date
2023-05-15
Last updated
2024-01-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ACL Injury, Rehabilitation After ACL Reconstruction, Accelerated Protocol

Brief summary

The main goal of a rehabilitation program after an ACL reconstruction is to regain mobility and muscle function and ultimately to return to sports participation. Purpose of the study: to investigate the effect of the accelerated rehabilitation program on knee pain, and function in patients post ACLR surgery. Fifty adult amateur males athletes who underwent ACLR surgery participated in this study, their age ranged from 18 to 35years.They were randomly assigned into two equal groups. Group (A) received accelerated rehabilitation protocol and group (B) received conventional physical therapy program. Treatment sessions were conducted 5 times per week for 22 weeks for both groups. All patients assessed pre and post treatment for pain intensity using visual analogue scale (VAS), and knee function using knee injury and osteoarthritis outcome score (KOOS), knee effusion, and LSI of Hop test.

Interventions

It's a four phases rehabilitation protocol mainly based on the remodeling process of the graft., emphasizing full passive knee extension, immediate weight bearing as tolerated and functional exercises

Sponsors

Delta University for Science and Technology
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients were participated in this study if they fulfilled the following criteria: * Underwent pre-operative rehabilitation program with minimal knee effusion and full extension, good patellofemoral mobility, and the patient can actively control the quadriceps. * Have an ACLR with an autolongous hamstring (HT) graft. * Age range from 18-40 years old. * Football players or who perform physically demanding work. * Have no other ligamentous injury. * Have nomeniscectomy previous to or simultaneouswith ACLR. * Have no cartilage damage.

Exclusion criteria

* • Patients younger than 18 or older than 35 years old * Have ACLR with any graft other than hamstring (HT) graft * Have ACL revision surgery * Have other ligamentous injury * Have a meniscectomy previous to or simultaneous with ACLR. * Had meniscal repair simultaneously with ACLR * Have cartilage damage.

Design outcomes

Primary

MeasureTime frameDescription
visual analogue scale22 weeksIt is a 100-mm horizontal line anchored by word descriptors at each end by no pain on the left and worst imaginable pain on the right

Secondary

MeasureTime frameDescription
Knee Injury and Osteoarthritis Outcome Score22 weeksit is a 42-item self-questionnaire with five subscales. A five-point scale ranging from 0 (no problem) to 4 (extreme problems) was used to score each item and the scores of each subscale were individually transformed into a 0-100 scale (0 = extreme knee problems, 100 = no knee problem)
limb symmetry index of Hop test battery22 weeksThe mean score of the results of each item of hop test battery of the injured limb was divided by the corresponding mean score of the uninjured limb and the result was multiplied by 100. Hop test battery consists of the following: (1) vertical jump, (2) hop for distance, (3) drop jump followed by a double hop for distance, (4) square hop and (5) side hop
knee effusion grading scale22 weeksIts a reliable and valid method which Based on a stroke test, where effusion of the knee joint is quantified using a 5-point scale. A 0 grade means no wave is produced with the downward stroke

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026