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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04864704
Other study ID # BradleyU
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 30, 2014
Est. completion date January 30, 2015

Study information

Verified date April 2021
Source Bradley University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

60 healthy participants were randomized into infraspinatus, erector spinae, or gastrocnemius groups. One session of dry needling DN was applied to the muscle in standardized location. Stiffness was assessed using a MyotonPRO at baseline, immediately post DN, and 24 hours later. The presence of a localized twitch response (LTR) during DN was used to subgroup participants.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date January 30, 2015
Est. primary completion date January 30, 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - men and women ages 18 to 65 years - reported good general health - tenderness or palpable trigger point in the muscle (infraspinatus, gastrocnemius, or erector spinae) Exclusion Criteria: - BMI > 30kg/m2 - surgery in the prior 12 months - current pain in the shoulder, low back, and lower leg - precautions to dry needling treatment (anticoagulant medications, bleeding disorders, known pregnancy)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
dry needling
Physical therapy

Locations

Country Name City State
United States Bradley University Peoria Illinois

Sponsors (1)

Lead Sponsor Collaborator
Bradley University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Stiffness Biomechanical stiffness of the muscle measured, non-invasively using a MyotonPRO. Stiffness (N/m) Change from baseline and immediately post intervention
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