- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05158582
Specific Modified Exercise Program for Low Back Pain in Racketlon Players
Comparison of Conventional Exercise Protocols and Specific Modified Exercise Program for Low Back Pain in Racketlon Players
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Racketlon is a combination sport in which competitors play a sequence of the four most popular racket sports: Table Tennis, Badminton, squash and tennis. Squash (racquet sport) is an intermittent high-intensity competitive racquet sport that requires quick movements as maintaining control over the placement of the ball with the greatest spatial awareness that is played globally through racquet sports are enjoyed throughout the world and are increasing in their popularity. Since this game encumbers a high level of fitness from the players, who are usually active for the majority of the playing time. Squash players are physically challenged as they are engaged in continuous repetitive training and frequent participation in game to improve their fitness and skills.
The purpose of this study is to find the effects of modified exercise program on LBP in racketlon players. The modified exercise program is a 5-Week Linear Periodization Program, which had effects on Maximal Strength and Speed on elite squash players. This study will find whether this 5-week linear periodization program has an effect to prevent low back pain in racketlon players.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab
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Rawalpindi, Punjab, Pakistan, 43600
- Safari Sports Club
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Active Male Racketlon player involved in sport activities for at least 3 times per week
- Age between 20-30 years.
- Players having ≥ 2 episodes of mechanical low back pain in past 6 months.
Exclusion Criteria:
Any upper and lower limb injury.
- History of metabolic diseases.
- History of recent fractures.
- History of spinal radiculopathy
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: SPECIFIC MODIFIED EXERCISE PROGRAM GROUP
The modified exercise group will perform 12 exercises.
|
The modified exercise program group will perform following exercises: Resisted static Squats SLER Banded rows SL Banded Jumps Resisted explosive reverse lunges 5hurdle Jumps Elevated single leg Swiss ball Bosu Banded Stars RLE Barbell lunge Static shoulder Abd.with banded leg Add Ant.Banded static squat with medball press Bosu banded superman Sit ups |
|
Active Comparator: CONVENTIONAL EXERCISES PROGRAM GROUP
The conventional exercises program will perform conventional exercises.
|
The conventional exercise program group will perform the same exercises as they doing for their low back pain.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Micheli functional scale (MFS):
Time Frame: 5 weeks
|
The Micheli functional scale (MFS) was developed as a back-specific tool for functional assessment in young athletes.
This scale is a brief and reliable rating scale to quantify pain intensity and athletic function and determines the degree of the back pain associated with sports activity limitations, back extension/or upright activities, sitting/or flexion activities, and jumping activity.
The MFS is a self-report questionnaire and contains 5 items consisting of a symptom question, 3 activity-related questions, and a visual analogue scale (VAS) for pain intensity.
The total score is calculated by adding questionnaire responses (range 0 - 15) plus VAS score (range 0 - 10).
This maximum total score of 25 is then multiplied by 4. The range of total scores is from 0 (least amount of difficulty) to 100 (the most amount of difficulty).
|
5 weeks
|
|
1 Minute Push-up Test (PUT):
Time Frame: 5 Weeks
|
The test began with the athlete in a push-up position, hands placed shoulder width apart with elbows in full extension.
The athlete was asked to maintain a neutral spine throughout the movement.
A 4-inch block was positioned directly below the athletes' chests to standardize push up depth every time. 1 repetition was counted when the athlete performs a push up and the chest comes into contact with the block and then returning to the starting position.
Each athlete was given 1 minute to perform a maximum number of repetitions.
|
5 Weeks
|
|
Kraus -Weber Test for lower back muscles
Time Frame: 5 Weeks
|
The Kraus-Weber Test involves a series of tests that measure minimum strength & flexibility of the back, abdominals, psoas, and hamstring muscles.
The Kraus-Weber fitness test protocols, a series of six medical fitness tests measuring the strength and flexibility of key postural (core) muscles.
This abdominal test assesses the strength of the abdominal and psoas muscles.
|
5 Weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Aadil Omer, Ph.D*, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/01018 Zainab Saad
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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