Bradley University
Peoria, Illinois, 61625, United States
NCT Number: NCT03876080
Investigation of the biomechanical response in delayed onset muscle soreness using dry needling vs. sham
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Notify Me18 year–35 year
All sexes
Interventional
Not applicable
Peoria, Illinois, 61625, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The use of a solid filiform needle to treat trigger points
Simulated needling
Time frame: baseline, immediately after intervention, 24 hours after intervention
Measuring Biomechanical stiffness ( N/m) change at the following time frames
Time frame: baseline, immediately after intervention, 24 hours after intervention
Measuring Pressure pain threshold change at the following time frames
Bradley University
Other
Biomechanical Response to Dry Needling in Subjects With Delayed Onset Muscle Soreness: a Double Blind Randomized Control Trial
Acronym: TDNDOMS
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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