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Pain and Neck Dysfunction Following Dry Needling With and Without Intramuscular Electrical Stimulus. — DNvDNES-2019  

Neck Pain Clinical Trial

Official title:
Pain and Neck Dysfunction Following Dry Needling With and Without Intramuscular Electrical Stimulus With 6 Week Follow Up

Clinical Trial Summary

Participants will be 18-59 years old who are recruited through a convenience sample from the UMHB/Belton community. There will be a randomized control trial consisting of three groups. Each participant will be assigned based on their order of entry to the study group assignment and then randomly organized via computer generation into 3 groups of 20 participants including a control group, a dry needling group (DN), and a dry needling E-stim group (DN-ES), resulting in approximately 60 total participants. Participants in the DN and DN-ES groups will be treated four times; at weeks 0, 2, 4 and 6 of the study. Data will be collected at weeks 4, 6 and 12 in all groups.

Clinical Trial Description

Interventions per group: Control: none DN: 20-30 seconds of DN per trigger point in each involved trapezius muscle, needles rest in situ 10 min, needles removed. DN-ES: 20-30 seconds of DN per trigger point (TrP) in each involved trapezius muscle, DC ES attached to needles crossing the most reactive TrP and current set to strong, but comfortable intensity at 10 MHz for 10 min, needles removed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04057781
Study type Interventional
Source University of Mary Hardin-Baylor
Contact
Status Completed
Phase N/A
Start date September 1, 2019
Completion date January 1, 2020
View Details
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