Objective: To evaluate the effectiveness of the TheraPoint Focal Pressure Support (TP-FPS) as a non-invasive treatment for pain associated with lateral Epicondylitis (LE). Design: Prospective cohort study. Participants: n = 25 study subjects (20 males and 5 females) ranging in age from 18-65 with pain in one upper limb either dominant (23) or non-dominant (2) associated with lateral epicondylitis for a minimum of six months. Interventions: Study participants were tasked to wear the TP-FPS for 3 hours per day for two weeks except when bathing or during main sleep hours. Outcome measures: Visual analog scale (VAS) pain score pre- and post-treatment period. Results: The combined (male and female) cohort average pre-treatment VAS pain score was 7.44 +/- 0.57. Post-treatment VAS pain score was 1.07 +/- 0.42, with a total reduction of 6.37 points and reached significance with p=0.0005. Male cohort demonstrated an average pre-treatment VAS pain score of 7.45 +/- 0.56. Post-treatment VAS pain score was 1.40 +/- 0.45, with a total reduction of 6.05 points and reached significance with p=0.006. Female cohort displayed an average pre-treatment VAS pain score of 7.40 +/- 1.92. Post-treatment VAS pain score was 1.70 +/- 1.14, with a total reduction of 5.70 and reached significance with p=0.001. No statistically significant difference was observed in the VAS pain score reduction between the male and female groups. Conclusion: The TP-FPS may indeed be a non-invasive therapeutic option for reducing pain associated with lateral epicondylitis.
Published in | American Journal of Sports Science (Volume 2, Issue 5) |
DOI | 10.11648/j.ajss.20140205.11 |
Page(s) | 111-114 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2014. Published by Science Publishing Group |
Lateral Epicondylitis, Elbow Pain, Non-Invasive, Pain Management, Pain Reduction
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APA Style
Christopher Bui. (2014). Lateral Epicondylitis: A Novel Non-Invasive Treatment Approach. American Journal of Sports Science, 2(5), 111-114. https://doi.org/10.11648/j.ajss.20140205.11
ACS Style
Christopher Bui. Lateral Epicondylitis: A Novel Non-Invasive Treatment Approach. Am. J. Sports Sci. 2014, 2(5), 111-114. doi: 10.11648/j.ajss.20140205.11
AMA Style
Christopher Bui. Lateral Epicondylitis: A Novel Non-Invasive Treatment Approach. Am J Sports Sci. 2014;2(5):111-114. doi: 10.11648/j.ajss.20140205.11
@article{10.11648/j.ajss.20140205.11, author = {Christopher Bui}, title = {Lateral Epicondylitis: A Novel Non-Invasive Treatment Approach}, journal = {American Journal of Sports Science}, volume = {2}, number = {5}, pages = {111-114}, doi = {10.11648/j.ajss.20140205.11}, url = {https://doi.org/10.11648/j.ajss.20140205.11}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajss.20140205.11}, abstract = {Objective: To evaluate the effectiveness of the TheraPoint Focal Pressure Support (TP-FPS) as a non-invasive treatment for pain associated with lateral Epicondylitis (LE). Design: Prospective cohort study. Participants: n = 25 study subjects (20 males and 5 females) ranging in age from 18-65 with pain in one upper limb either dominant (23) or non-dominant (2) associated with lateral epicondylitis for a minimum of six months. Interventions: Study participants were tasked to wear the TP-FPS for 3 hours per day for two weeks except when bathing or during main sleep hours. Outcome measures: Visual analog scale (VAS) pain score pre- and post-treatment period. Results: The combined (male and female) cohort average pre-treatment VAS pain score was 7.44 +/- 0.57. Post-treatment VAS pain score was 1.07 +/- 0.42, with a total reduction of 6.37 points and reached significance with p=0.0005. Male cohort demonstrated an average pre-treatment VAS pain score of 7.45 +/- 0.56. Post-treatment VAS pain score was 1.40 +/- 0.45, with a total reduction of 6.05 points and reached significance with p=0.006. Female cohort displayed an average pre-treatment VAS pain score of 7.40 +/- 1.92. Post-treatment VAS pain score was 1.70 +/- 1.14, with a total reduction of 5.70 and reached significance with p=0.001. No statistically significant difference was observed in the VAS pain score reduction between the male and female groups. Conclusion: The TP-FPS may indeed be a non-invasive therapeutic option for reducing pain associated with lateral epicondylitis.}, year = {2014} }
TY - JOUR T1 - Lateral Epicondylitis: A Novel Non-Invasive Treatment Approach AU - Christopher Bui Y1 - 2014/09/20 PY - 2014 N1 - https://doi.org/10.11648/j.ajss.20140205.11 DO - 10.11648/j.ajss.20140205.11 T2 - American Journal of Sports Science JF - American Journal of Sports Science JO - American Journal of Sports Science SP - 111 EP - 114 PB - Science Publishing Group SN - 2330-8540 UR - https://doi.org/10.11648/j.ajss.20140205.11 AB - Objective: To evaluate the effectiveness of the TheraPoint Focal Pressure Support (TP-FPS) as a non-invasive treatment for pain associated with lateral Epicondylitis (LE). Design: Prospective cohort study. Participants: n = 25 study subjects (20 males and 5 females) ranging in age from 18-65 with pain in one upper limb either dominant (23) or non-dominant (2) associated with lateral epicondylitis for a minimum of six months. Interventions: Study participants were tasked to wear the TP-FPS for 3 hours per day for two weeks except when bathing or during main sleep hours. Outcome measures: Visual analog scale (VAS) pain score pre- and post-treatment period. Results: The combined (male and female) cohort average pre-treatment VAS pain score was 7.44 +/- 0.57. Post-treatment VAS pain score was 1.07 +/- 0.42, with a total reduction of 6.37 points and reached significance with p=0.0005. Male cohort demonstrated an average pre-treatment VAS pain score of 7.45 +/- 0.56. Post-treatment VAS pain score was 1.40 +/- 0.45, with a total reduction of 6.05 points and reached significance with p=0.006. Female cohort displayed an average pre-treatment VAS pain score of 7.40 +/- 1.92. Post-treatment VAS pain score was 1.70 +/- 1.14, with a total reduction of 5.70 and reached significance with p=0.001. No statistically significant difference was observed in the VAS pain score reduction between the male and female groups. Conclusion: The TP-FPS may indeed be a non-invasive therapeutic option for reducing pain associated with lateral epicondylitis. VL - 2 IS - 5 ER -