← Eichor
Study identifier: NCT07438522 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Isometric and Isotonic Hand Strengthening in Competitive Female Badminton Athletes

Condition: Athletic Performance and Injury Risk  ·  Sponsor: Riphah International University

PhaseNA
Planned participants32
Who can joinFemale, 18 Years to 30 Years
Healthy volunteersYes

About this study

This randomized clinical trial aims to determine the effects of targeted isometric and isotonic hand strengthening exercises on hand function, dexterity, grip strength and grip endurance in competitive female badminton athletes aged 18-30 years. Participants will be randomly allocated into two groups receiving either isometric or isotonic hand strengthening exercise programs performed three times per week for six weeks. Outcome measures will be assessed at baseline, 3rd week and 6th week using Michigan Hand Outcomes Questionnaire (MHQ), Purdue Pegboard Test or Nine-Hole Peg Test, Hand Dynamometer Test and Sustained Grip Test.

This description comes directly from the study's public registry record.

Talk to the study team

Danish Hassan, PhD  ·  +92 345 7946009  ·  danish.hassan009@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Punjab Sports BoardLahore, Punjab Province, PakistanRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07438522