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Clinical Trials/CTRI/2025/08/092253
CTRI/2025/08/092253
Not yet recruiting
Not Applicable

Influence of a multiplanar lumbopelvic stability program on overhead deep squat pattern and dynamic knee valgus in collegiate athletes by using 2d kinematic analysis. A randomized control trial

Vydehi Institute of Physiotherapy, Vydehi Group of Institutions1 site in 1 country90 target enrollmentStarted: September 1, 2025Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Vydehi Institute of Physiotherapy, Vydehi Group of Institutions
Enrollment
90
Locations
1
Primary Endpoint
Unilateral Hip Bridge Endurance Test

Overview

Brief Summary

This double-blinded randomized controlled trial aims to assess the effectiveness of the multiplanar lumbopelvic stability program and the traditional core stability program. Lumbopelvic stability is essential for injury prevention and performance in dynamic movements like deep squats, and dynamic knee valgus, the inward collapse of the knee, poses injury risks.

Participants will be randomly allocated into two groups: Group A will receive the multiplanar lumbopelvic stability program along with conventional core stability training, and Group B will receive only conventional core stability training.

Both interventions will be administered as four exercise sessions for a week, a total of 16 sessions. Each session will follow standardized parameters and treatment duration under the supervision of a trained physiotherapist. These interventions are safe, noninvasive, drug-free, and simple to administer, with minimal to no side effects, making them suitable for routine clinical use.

The study population will be recruited based on the selection criteria.

The following outcome measures will be assessed: Unilateral Hip Bridge Endurance Test, Landing Error Scoring System, Deep Overhead Squat Test, Frontal Plane Projection Angle. A basic musculoskeletal physiotherapy assessment will be carried out before intervention. Outcome assessments will be conducted across three timelines: one at baseline, a second at the completion of 4 weeks, and a third at the 16th week to evaluate the treatment effects.

All participants will receive a participant information sheet that clearly outlines the study’s purpose, procedures, potential benefits, and risks. Written informed consent will be obtained prior to participation, ensuring full understanding, confidentiality, and voluntary involvement. Participants may withdraw from the study at any point without penalty.

This trial aims to assess the effectiveness of the Multiplanar Lumbopelvic Stability Program in influencing the overhead deep squat pattern and addressing dynamic knee valgus among collegiate athletes, which can provide valuable insights into the impact of the intervention on biomechanics, ultimately contributing to the optimization of training protocols, reduction of injury risks, and promotion of long-term musculoskeletal health in collegiate sports.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant and Outcome Assessor Blinded

Eligibility Criteria

Ages
17.00 Year(s) to 25.00 Year(s) (—)
Sex
Male

Inclusion Criteria

  • Male subjects are included Age between 17 years and 25 years Males who play recreational volleyball, basketball, and Football and playing on average 2 times or less than that in a week Subjects with poor lumbopelvic control with positive findings of the following procedures: Knee Lift Abdominal Test, Bend Knee Fall-Out, Active Straight Leg Raising and PRONE Test by using Pressure Biofeedback Unit.

Exclusion Criteria

  • Age less than 17 years or more than 25 years History of Low back injury or severe lower extremity injuries within the previous 6 months Any known neuromuscular disorders and any other systemic disorders Unwillingness of the participant.

Outcomes

Primary Outcomes

Unilateral Hip Bridge Endurance Test

Time Frame: Baseline, 4 weeks and 16 weeks

Landing Error Scoring System

Time Frame: Baseline, 4 weeks and 16 weeks

Deep Overhead Squat Test

Time Frame: Baseline, 4 weeks and 16 weeks

Frontal Plane Projection Angle

Time Frame: Baseline, 4 weeks and 16 weeks

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Vydehi Institute of Physiotherapy, Vydehi Group of Institutions
Sponsor Class
Private medical college
Responsible Party
Principal Investigator
Principal Investigator

Srinivasulu M

Saveetha College of Physiotherapy, Saveetha Institute of Medical and Technical Sciences

Study Sites (1)

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