Isometric and Isotonic Hand Strengthening in Competitive Female Badminton Athletes (NCT07438522) | Clinical Trial Compass
RecruitingNot Applicable
Isometric and Isotonic Hand Strengthening in Competitive Female Badminton Athletes
Pakistan32 participantsStarted 2025-12-01
Plain-language summary
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.
Who can participate
Age range
18 Years – 30 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Female badminton athletes
* Age between 18-30 years
* Right-hand dominant
* Minimum 2 years of competitive badminton experience
Exclusion Criteria:
* History of upper limb injury in last 6 months
* Cardiovascular or metabolic disorder limiting exercise
* Medication affecting muscle performance
* Current upper limb rehabilitation program participation
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.