Effects of Battle Rope Training Program On Bocce Throwing In Young Adaptive Bocce Players

NCT06955065 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 18

Last updated 2025-05-25

No results posted yet for this study

Summary

This randomized controlled trial aims to evaluate the effectiveness of battle rope training in enhancing athletic performance among young adaptive bocce players aged 10 to 18 years. A total of 18 participants with physical disabilities qualifying them for adaptive sports, capable of following instructions and without recent injuries or surgeries, will be randomly assigned to either an experimental group undergoing structured battle rope training or a control group continuing regular bocce training. The 8-week intervention, conducted three times per week, focuses on improving upper body strength, endurance, and coordination. Pre- and post-intervention assessments will include bocce throwing accuracy and distance, grip strength, number of rope slams in a set time, and shoulder endurance, with a dynamometer used to measure strength metrics. Data will be analyzed using SPSS version 23 to determine the impact of battle rope training on performance and fitness in adaptive sports

Conditions

  • Special Senses Disorders

Interventions

OTHER

battle rope training

Battle rope training is a dynamic, high-intensity exercise involving heavy ropes to improve strength, endurance, and coordination. It primarily targets the upper body, including the shoulders, arms, and core, through rhythmic, wave-like movements. This training is adaptable and effective for enhancing functional fitness in both general and adaptive athletes.

OTHER

Bocce Throwing

Participants in the control group will engage in regular bocce training sessions as per their usual routine. These sessions will focus on standard bocce drills and techniques without additional battle rope exercise. A warm- up activity used in every training session and a proper warm-up should include Aerobic activity and Dynamic stretching . 15 to 20 repetitions of each exercise.

Sponsors & Collaborators

  • Riphah International University

    lead OTHER

Principal Investigators

  • khadija kiran, MS-PPT · Riphah International University

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
10 Years
Max Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-02-15
Primary Completion
2025-07-15
Completion
2025-07-31

Countries

  • Pakistan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06955065 on ClinicalTrials.gov