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Study of the effects of dry needling on fatigue

Not Applicable
Recruiting
Conditions
fatigue.
Registration Number
IRCT20221201056676N1
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
20
Inclusion Criteria

no history of lower extremity injury
no vestibular disorders
no cardio-vascular-pulmunary diseases
no neuromusculoskeletal diseases
age of 18-40 years
minimum exercise of 1-hour, 3 sessions per week (at least 2 months)
no pain in lower extremity in at least recent 2 months
no Trypanophobia (needle phobia)
no needle contradictions
no history of dry needle experience

Exclusion Criteria

lack of consent
have pain during the study
inability to continue the test
have strenuous physical activity 48 hours before the test
being a physical therapy student

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Maximum isometric torque of quadriceps. Timepoint: measuring maximum isometric torque of quadriceps at the beginning of the study, after fatigue protocol, after intervention, and one hour after intervention. Method of measurement: handheld dynamometer.;Function. Timepoint: measuring function at the beginning of the study, after fatigue protocol, after intervention, and one hour after intervention. Method of measurement: single leg hop test.;H/M ratio. Timepoint: measuring H/M ratio at the beginning of the study, after fatigue protocol, after intervention, and one hour after intervention. Method of measurement: electromyography (EMG).
Secondary Outcome Measures
NameTimeMethod
Balance. Timepoint: measuring balance at the beginning of the study, after fatigue protocol, after intervention, and one hour after intervention. Method of measurement: single leg stance test.
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