- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07725016
Functional Movement Training Versus Functional Stability Training in Post-ACL Surgery
Effects of Functional Movement Training Versus Functional Stability Training on Stregth, Balance and Performance in Athelets With Post-ACL Reconstruction
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Athletes involves fast movement and intense activity which places great stress on the leg muscles and increases the chances of ACL injuries. Changing direction quickly, jumping and landing strangely or encountering another person or an object can result in these injuries. Rehabilitation efforts after ACL reconstruction should cover strengthening the joint and enhancing neuromuscular skills that athletes need for their sporting activities. It is hypothesized that following rehabilitation protocols involving functional movements and stability exercises may improve control of muscles, make joints more stable and lead to safer movement techniques. Aiming to see the effects of Functional Movement Training compared to Functional Stability Training on function and stability post-ACL surgery in athletes, this study will investigate their meaning.
This randomized controlled trial study will include 32 athletes aged 18-35 who had ACL surgery. After surgery, participants will be selected and assigned randomly to the Functional Movement Training or Functional Stability Training groups. The Functional Movement Training protocol will include exercise: deep squat, hurdle step, in-line lunge, active straight leg raise, trunk stability push-up, and rotatory stability etc. The Functional Stability Training protocol will emphasize exercises Single-leg squats, Balance boards or BOSU ball training, Planks and side planks., Step-ups, lunges, and agility drills. Both exercises will be performed 3 times per week for 8 weeks. The main goals will be to assess pain, balance and function and knee stability. The Numeric Pain Rating Scale (NPRS), Japanese Knee Questionnaire (JACL 25) and PRSI tools will be used for collecting data. The analysis will be conducted with SPSS software and it will include use of descriptive statistics, Normality test, independent t-tests, and paired t-tests. The significance level will be p < 0.05 for this study.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Amna Shahid, t-dpt
- Phone Number: 0334-4512823
- Email: amna.shahid@riphah.edu.pk
Study Locations
-
-
Punjab Province
-
Lahore, Punjab Province, Pakistan, 54660
- Recruiting
- Sheikh zayed hospital Lahore
-
Contact:
- Amna Shahid, T-DPT
- Phone Number: 03344512823
- Email: amna.shahid@riphah.edu.pk
-
Contact:
- Rimza Ramzan
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male Athletes
- Athletes aged between 18-35 years
- Athletes who have undergone ACL reconstructive surgery within the previous 3-6 months .
Exclusion Criteria:
- History of multiple knee surgeries (meniscus repair, partial meniscectomy, or cartilage repair) Other lower limb injuries affecting rehabilitation
- Systemic illnesses affecting musculoskeletal function
- Individuals with alcohol or drug abuse issues
- Those involved in other weight and balance training programs
Study Plan
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 |
|---|---|
|
Experimental: Functional Movement training
Funtional movement training
|
The Functional Movement Training protocol will include exercise: deep squat, hurdle step, in-line lunge, active straight leg raise, trunk stability push-up, and rotatory stability etc.
|
|
Experimental: Functional stability training
|
The Functional Stability Training protocol will emphasize exercises Single-leg squats, Balance boards or BOSU ball training, Planks and side planks., Step-ups, lunges, and agility drills.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Through NPRS
Time Frame: Pre and 6 week post interventional
|
Pain through NPRS
|
Pre and 6 week post interventional
|
|
Stablity and function through JACL-25
Time Frame: Pre and 6 week post interventional
|
Stablity and function through JACL-25
|
Pre and 6 week post interventional
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Rimza Ramzan, DPT, Study Principal Investigator
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR & AHS/25/0420
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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