TY - JOUR
T1 - Radial extracorporeal shock wave device appearance does not influence clinical outcomes
T2 - A randomized controlled trial
AU - Morral, Antoni
AU - Urrútia, Gerard
AU - Gich, Ignasi
AU - Ruiz, Reme
AU - Bonfill, Xavier
N1 - Publisher Copyright:
© 2019 Foundation of Rehabilitation Information.
PY - 2019/3
Y1 - 2019/3
N2 - Objective: To determine whether the appearance of a radial extracorporeal shock wave device affects clinical outcomes in chronic plantar fasciitis. Study design: Randomized controlled parallel assessor- blinded clinical trial. Material and methods: A total of 135 patients were assigned to 3 groups: Group I, standard radial extracorporeal shock wave device; group II, standard radial extracorporeal shock wave device modified to give a more sophisticated appearance; group III, standard radial extracorporeal shock wave device modified to give a more austere appearance. The radial extracorporeal shock waves emitted by the 3 devices were identical. Primary outcome was foot function, measured with the Foot Function Index. Secondary outcomes were pain at different times, measured with a visual analogue scale, and plantar fascia thickness, measured with ultrasound. Results: All variables decreased significantly from baseline assessment, in all 3 groups and at all timepoints: 1, 2, 4 and 14 months after the last session (p < 0.001). There were no significant differences between groups for any of the variables assessed. Conclusion: Device appearance had no statistically significant influence on clinical outcomes in patients with chronic plantar fasciitis treated with radial extracorporeal shock wave therapy.
AB - Objective: To determine whether the appearance of a radial extracorporeal shock wave device affects clinical outcomes in chronic plantar fasciitis. Study design: Randomized controlled parallel assessor- blinded clinical trial. Material and methods: A total of 135 patients were assigned to 3 groups: Group I, standard radial extracorporeal shock wave device; group II, standard radial extracorporeal shock wave device modified to give a more sophisticated appearance; group III, standard radial extracorporeal shock wave device modified to give a more austere appearance. The radial extracorporeal shock waves emitted by the 3 devices were identical. Primary outcome was foot function, measured with the Foot Function Index. Secondary outcomes were pain at different times, measured with a visual analogue scale, and plantar fascia thickness, measured with ultrasound. Results: All variables decreased significantly from baseline assessment, in all 3 groups and at all timepoints: 1, 2, 4 and 14 months after the last session (p < 0.001). There were no significant differences between groups for any of the variables assessed. Conclusion: Device appearance had no statistically significant influence on clinical outcomes in patients with chronic plantar fasciitis treated with radial extracorporeal shock wave therapy.
KW - nocebo effect
KW - placebo effect
KW - plantar fasciitis
KW - shock wave, therapeutic context.
UR - http://www.scopus.com/inward/record.url?scp=85062867142&partnerID=8YFLogxK
U2 - 10.2340/16501977-2516
DO - 10.2340/16501977-2516
M3 - Article
C2 - 30667512
AN - SCOPUS:85062867142
SN - 1650-1977
VL - 51
SP - 201
EP - 208
JO - Journal of Rehabilitation Medicine
JF - Journal of Rehabilitation Medicine
IS - 3
ER -