Effects of Dry Needling on Vertical Jump Performance (NCT06184672) | Clinical Trial Compass
UnknownNot Applicable
Effects of Dry Needling on Vertical Jump Performance
24 participantsStarted 2024-02-08
Plain-language summary
ChatGPT ChatGPT Injury prevention and performance enhancement have become two of the main goals in every sport. Myofascial Pain Syndrome is primarily caused by myofascial trigger points, which may result in referred pain, stiffness, shortening, and/or muscle weakness.
The aim of this study is to assess the effects of dry needling on latent myofascial trigger points (LTMTP) and its impact on vertical jump height in female volleyball players.
The study is a single-blind, randomized controlled clinical trial conducted on healthy female volleyball practitioners with no lower limb injuries in the last 6 months. Participants must exhibit LMTP in the triceps surae muscles and be familiar with the counter-movement jump (CMJ) test. Subjects will be randomly assigned to either a control group or an intervention group.
Who can participate
Age range
18 Years – 25 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:
* No lower limb injuries in the last 6 months
* Presence of latent MTPs in gastrocnemius
* Be familiar with performing CMJ tests
Exclusion Criteria:
* Needle phobia
* Presence of active MTPs in the lower limb
* Any pathology that prevented the use of dry needling
* Any pathology that prevented the performance of CMJ test.
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.