- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06587516
Neuromuscular Warm-Up Program for Badminton Players (NWUPFBM)
Developing a Novel Neuromuscular Warm-Up Program for Recreational Badminton Players: An Experimental Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study investigates the effectiveness of a novel neuromuscular warm-up program tailored for recreational badminton players. The program is designed to improve balance, enhance movement efficiency and reduce the risk of injuries commonly associated with badminton.
Participants will be recruited from recreational badminton clubs and will undergo baseline assessments of balance performance and lunge movement using motion capture (Mocap), EMG. and inertia measurement unit (IMU). The warm-up program includes a series of targeted exercises selected based on expert consensus from a previous Delphi study. These exercises focus on key areas such as dynamic stability, and proprioception.
Participants perform pre and post test with Star Excursion Balance Test (SEBT) and forward lunge movement with (IMU, MOcap and MEG) attached on the lower limb. The intervention will be: 1) novel neuromuscular warmup and 2) traditional warmup. Participants will perform both the warmup but on different days with one day rest in between the interventions.
The study's findings aim to inform best practices for warm-up routines in badminton, potentially offering a standardized program that can be widely adopted by recreational players to enhance their performance and safety on the court.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Kuala Lumpur, Malaysia, 50603
- University of Malaya
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Injury free for >1 year, plays badminton minimum of once a week, have experience of playing at least 3 years
Exclusion Criteria:
- Badminton players that participate in competition in any level (novice, intermediate or elite tier), involve in any regimented training, participants with any joint disorder, non-communicable diseases (NCD), neurologically unstable, consumption of any medication that can interfere with performance.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Experimental
badminton players who plays badminton socially once a week with minimum experience of three years
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This intervention consists of a structured warm-up routine specifically designed to enhance neuromuscular function and balance.
The program includes exercises such as two way forward lunge, single-leg balance, multidirectional lunges, single-leg hops forward and backward, and single-leg calf raises.
Each exercise is aimed at improving proprioception, dynamic stability, and lower limb strength.
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Active Comparator: Control
badminton players who plays badminton socially once a week with minimum experience of three years
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This intervention involves a conventional warm-up program.
It includes general stretching exercises and light jogging intended to prepare the body for physical activity.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Balance Performance
Time Frame: pre-test conducted immediately before the intervention and a post-test conducted immediately after the intervention
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Balance will be measured using standardised tests such as the Star Excursion Balance Test (SEBT), which evaluates the participant's reach distances in multiple directions
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pre-test conducted immediately before the intervention and a post-test conducted immediately after the intervention
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Ankle Movement
Time Frame: pre-test conducted immediately before the intervention and a post-test conducted immediately after the intervention.
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This measure will assess the angle of (dorsi-flexion and plantar-flexion) and (inversion and eversion) at the ankle joint during the lunge movement.
The aim is to evaluate changes in ankle joint alignment and range of motion as a result of the neuromuscular warm-up program.
Ankle angles will be measured using motion capture technology and an inertial measurement unit (IMU) to provide accurate and objective data.
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pre-test conducted immediately before the intervention and a post-test conducted immediately after the intervention.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Neuromuscular Activity
Time Frame: pre-test conducted immediately before the intervention and a post-test conducted immediately after the intervention
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This measure will evaluate neuromuscular activity using electromyography (EMG) to assess muscle activation patterns during the lunge movement.
EMG sensors will be placed on key muscles involved in the lunge, such as the quadriceps, hamstrings, and calf muscles, to record electrical activity.
This data will help determine the impact of the neuromuscular warm-up program on muscle activation, coordination, and overall neuromuscular function during dynamic movements.
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pre-test conducted immediately before the intervention and a post-test conducted immediately after the intervention
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Saranya Navaratnarajah, Institute for Advanced Studies, Universiti Malaya
Publications and helpful links
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 (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
- UM.TNC2/UMREC_3398
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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