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Study identifier: NCT07550543 Synced from ClinicalTrials.gov · July 29, 2026
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PEMF Therapy in Shoulder Tendinopathy

Condition: Shoulder Tendinopathy  ·  Sponsor: Balnear and Rehabilitation Sanatorium Techirghiol

PhaseNA
Planned participants60
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to evaluate whether pulsed electromagnetic field (PEMF) therapy delivered via the Super Inductive System (SIS), integrated into a multimodal rehabilitation program, improves pain, function, pressure pain threshold, muscle strength, psychological status, and quality of life in adults with shoulder tendinopathies. The main questions it aims to answer are: * Does the addition of PEMF (SIS) therapy reduce pain intensity and improve pressure pain threshold compared to standard balneophysiotherapy? * Does PEMF (SIS) therapy improve shoulder function, muscle strength, psychological status, and quality of life? The study will compare a multimodal rehabilitation program supplemented with PEMF (SIS) therapy to standard balneophysiotherapy to determine whether the addition of PEMF (SIS) provides superior clinical outcomes. Participants will: * Undergo a multimodal rehabilitation program including balneophysiotherapy * Be assigned to receive either standard treatment or treatment supplemented with PEMF (SIS) therapy * Be evaluated at baseline (admission), immediately after treatment completion (discharge), and at 4 weeks after treatment using validated clinical instruments assessing pain, function, pressure pain threshold, muscle strength, psychological status, depressive symptoms, and quality of life.

This description comes directly from the study's public registry record.

Talk to the study team

Alexandra E Ciota, PhD Student  ·  +40723662300  ·  alexandra.ciota@365.univ-ovidius.ro

Always discuss trial participation with your own doctor first.

Locations (1)

Balneal and Rehabilitation Sanatorium of TechirghiolConstanța, Techirghiol, RomaniaRecruiting

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Source record: clinicaltrials.gov/study/NCT07550543