scholarly journals Effects of Trigger Point Dry Needling on Neuromuscular Performance and Pain of Individuals Affected by Patellofemoral Pain: A Randomized Controlled Trial

2020 ◽  
Vol Volume 13 ◽  
pp. 1677-1686
Author(s):  
Yan-Tao Ma ◽  
Li-Hui Li ◽  
Qi Han ◽  
Xiao-Lei Wang ◽  
Pei-Yu Jia ◽  
...  
Keyword(s):  
Randomized Controlled Trial ◽  
Trigger Point ◽  
Controlled Trial ◽  
Patellofemoral Pain ◽  
Dry Needling ◽  
Neuromuscular Performance ◽  
Randomized Controlled

Postneedling Soreness and Tenderness After Different Dosages of Dry Needling of an Active Myofascial Trigger Point in Patients With Neck Pain: A Randomized Controlled Trial

PM&R ◽  
2018 ◽  
Vol 10 (12) ◽  
pp. 1311-1320 ◽  
Author(s):  
Aitor Martín-Pintado-Zugasti ◽  
Josué Fernández-Carnero ◽  
Jose Vicente León-Hernández ◽  
Cesar Calvo-Lobo ◽  
Hector Beltran-Alacreu ◽  
...  
Keyword(s):  
Randomized Controlled Trial ◽  
Neck Pain ◽  
Trigger Point ◽  
Controlled Trial ◽  
Myofascial Trigger Point ◽  
Dry Needling ◽  
Randomized Controlled

scholarly journals Effectiveness of Trigger Point Dry Needling for Plantar Heel Pain: A Randomized Controlled Trial

2014 ◽  
Vol 94 (8) ◽  
pp. 1083-1094 ◽  
Author(s):  
Matthew P. Cotchett ◽  
Shannon E. Munteanu ◽  
Karl B. Landorf
Keyword(s):  
Randomized Controlled Trial ◽  
Adverse Events ◽  
Trigger Point ◽  
Controlled Trial ◽  
Heel Pain ◽  
Foot Pain ◽  
Dry Needling ◽  
Randomized Controlled ◽  
Plantar Heel Pain ◽  
End Point

Background Plantar heel pain can be managed with dry needling of myofascial trigger points; however, there is only poor-quality evidence supporting its use. Objective The purpose of this study was to evaluate the effectiveness of dry needling for plantar heel pain. Design The study was a parallel-group, participant-blinded, randomized controlled trial. Setting The study was conducted in a university health sciences clinic. Patients Study participants were 84 patients with plantar heel pain of at least 1 month's duration. Intervention Participants were randomly assigned to receive real or sham trigger point dry needling. The intervention consisted of 1 treatment per week for 6 weeks. Participants were followed for 12 weeks. Measurements Primary outcome measures included first-step pain, as measured with a visual analog scale (VAS), and foot pain, as measured with the pain subscale of the Foot Health Status Questionnaire (FHSQ). The primary end point for predicting the effectiveness of dry needling for plantar heel pain was 6 weeks. Results At the primary end point, significant effects favored real dry needling over sham dry needling for pain (adjusted mean difference: VAS first-step pain=−14.4 mm, 95% confidence interval [95% CI]=−23.5 to −5.2; FHSQ foot pain=10.0 points, 95% CI=1.0 to 19.1), although the between-group difference was lower than the minimal important difference. The number needed to treat at 6 weeks was 4 (95% CI=2 to 12). The frequency of minor transitory adverse events was significantly greater in the real dry needling group (70 real dry needling appointments [32%] compared with only 1 sham dry needling appointment [<1%]). Limitations It was not possible to blind the therapist. Conclusion Dry needling provided statistically significant reductions in plantar heel pain, but the magnitude of this effect should be considered against the frequency of minor transitory adverse events.

Strengthening of the hip posterolateral musculature versus hip anteromedial musculature in patients with patellofemoral pain: A randomized controlled trial

2021 ◽  
Vol 47 ◽  
pp. e5
Author(s):  
Carlos Augusto Silva Rodrigues ◽  
Helena Larissa das Neves Rodrigues ◽  
Bruno Augusto Lima Coelho ◽  
Pedro Olavo de Paula Lima ◽  
Gabriel Peixoto Leão Almeida
Keyword(s):  
Randomized Controlled Trial ◽  
Controlled Trial ◽  
Patellofemoral Pain ◽  
Randomized Controlled
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