Dry Needling in Subjects With Delayed Onset Muscle Soreness

NCT03876080 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2023-07-27

No results posted yet for this study

Summary

Investigation of the biomechanical response in delayed onset muscle soreness using dry needling vs. sham

Conditions

  • Delayed Onset Muscle Soreness

Interventions

OTHER

Dry needling

The use of a solid filiform needle to treat trigger points

OTHER

Sham needling

Simulated needling

Sponsors & Collaborators

  • Bradley University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-03-30
Primary Completion
2023-05-23
Completion
2023-05-23

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03876080 on ClinicalTrials.gov