Comparative Effects of Rebound Training and Theraband Resistance Exercise in Badminton Players

October 24, 2024 updated by: Riphah International University

Comparative Effects of Rebound Training and Theraband Resistance Exercise on Agility, Power and Dynamic Balance in Badminton Players With Patellofemoral Pain Syndrome

Comparative Effects of Rebound Training and Theraband Resistance Exercise in Badminton Players With Patellofemoral Pain Syndrome

Study Overview

Status

Active, not recruiting

Conditions

Intervention / Treatment

Detailed Description

Comparative Effects of Rebound Training and Theraband Resistance Exercise on agility, power and dynamic balance in Badminton Players With Patellofemoral Pain Syndrome

Study Type

Interventional

Enrollment (Actual)

24

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Pakistan
    • Punjab
      • Lahore, Punjab, Pakistan, 05450
        • Pakistan Sports Board

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Females
  • Age 18 to 25 years
  • Positive Patellofemoral Compression Test ( Pain is in around the patella and back of knee cap) With playing experience of 3 years will be included
  • Minimum Sports activity 1 hour 4 times a week

Exclusion Criteria:

  • Recreational players
  • Players with recent injury in past 6 months
  • Any musculoskeletal and neurological problem
  • Player addicted to any drug or alcohol will be excluded

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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: Group A
12 Participants will be in experimental group A. They will perform rebound training for six weeks. Measure all values before giving them protocol and after protocol.
Other: Rebound Training
12 participants will be in experimental group A giving them rebound training.
Experimental: Group B
12 Participants will be in experimental group B. They will perform theraband resistance exercise for six weeks. Measure all values before giving them protocol and after protocol.
Other: Theraband resistance exercise
12 participants will be in experimental group A giving them theraband resistance exercise with different band resistnce.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Numeric Pain Rating Scale
Time Frame: 6 weeks
Numeric Pain Rating Scale NPRS is based on 11-point numerical rating scale for determining pain intensity, 0(no pain) to 10(worst pain imaginable) pain intensity .NRS pain has high validity and reliability (β = 0.42 [95% CI 0.04, 0.80]
6 weeks
Agility T Test
Time Frame: 6 Weeks
Agility will be measured by the agility T - tests high intra-trail reliability of the test (ICC=0.98). The participants were instructed to run 9.14 meters from the starting line to the first cone, touch the tip with their right hand, shuffle 4.57 meters to the left to the second cone, shuffle 9.14 meters to the right to the third cone, touch with their right hand, shuffle 4.57 meters to the left to the middle cone, touch with their left hand, and then back pedal to the starting line.
6 Weeks
Vertical Jump Power Test
Time Frame: 6 Weeks
To mark the wall at the height of their jump, the participant applies chalk to the tips of their fingers. After standing away from the wall, the individual uses both arms and legs to help project their body upwards and jumps as high as they can. At the peak of the jump, try to make contact with the wall. Power will be measured by Sargent Test. Vertical Jump test is a very common test for measuring explosive leg power intra rater class reliability ICC = 0.903 to 0.934)
6 Weeks
40-Yd Speed Test
Time Frame: 6 Weeks
Speed will be measured by 40-Yd Sprint Test. The test involves running a single maximum sprint over 40 yards, with the time recorded. The aim of this test will be determine 40-Yd Sprint. Sprints of 40 yd were used to determine quickness ICC > 0.987
6 Weeks
Star Excursion Dynamic Balance
Time Frame: 6 Weeks
The SEBT is a functional test that incorporates a single-leg stance on one leg with maximum reach of the opposite leg. The SEBT is performed with the subject standing at the center of a grid placed on the floor, with 8 lines extending at 45° increments from the center of the grid. The 8 lines positioned on the grid are labeled according to the direction of excursion relative to the stance leg. The plane was constructed in a facility with the help of protractor and adhesive tape on the hard tile floor. Dynamic balance check with balance with Star Excursion Balance Test (SEBT) the intra class correlation coefficients ( 0.86 to 0.92)
6 Weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Riphah International University

Investigators

  • Principal Investigator: Noor Fatima, DPT, Riphah International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 24, 2024

Primary Completion (Estimated)

November 24, 2024

Study Completion (Estimated)

December 10, 2024

Study Registration Dates

First Submitted

October 24, 2024

First Submitted That Met QC Criteria

October 24, 2024

First Posted (Actual)

October 26, 2024

Study Record Updates

Last Update Posted (Actual)

October 26, 2024

Last Update Submitted That Met QC Criteria

October 24, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REC/RCR&AHS/24/0413

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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