Medicine Ball Throw and Resistance Band Training Among Bowlers

NCT07440745 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 56

Last updated 2026-02-27

No results posted yet for this study

Summary

This study will be Randomized clinical trial and will recruit male/female cricket bowlers aged 18-30yrs. Participants will be randomly divided into two groups and will perform training sessions three times per week for eight weeks. Group A will engage in medicine ball throw training while Group B will participate in resistance band training. The purpose of this study is to compare the effects of these two training programs on dynamic strength and bowling accuracy among cricket bowlers.

Conditions

  • Sports Physical Therapy

Interventions

OTHER

Medicine ball throw training

Participants will perform Medicine Ball Throw training focusing on chest pass, overhead throw, and rotational throw exercises to enhance dynamic strength and power in bowlers. The training program will be conducted three times per week for eight weeks under supervision, with progressive loading applied according to participant tolerance.

OTHER

Resistance band training

Participants will perform Resistance Band training consisting of upper extremity and trunk strengthening exercises using elastic resistance bands in cricket bowlers. The training program will be conducted three times per week for eight weeks under supervision, with progressive resistance applied throughout the intervention period.

Sponsors & Collaborators

  • Riphah International University

    lead OTHER

Principal Investigators

  • Muhammad Hashim Hashim, pp-dpt · Riphah International University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
30 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-03-18
Primary Completion
2025-10-15
Completion
2025-11-07

Countries

  • Pakistan

More Related Trials

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 NCT07440745 on ClinicalTrials.gov