Effects of capacitive and resistive electric transfer therapy in patients with painful shoulder impingement syndrome: a comparative study.
T Paolucci, L Pezzi, M A Centra...
https://pubmed.ncbi.nlm.nih.gov/31680597/Actively Recruiting
Led by Aristotle University Of Thessaloniki · Updated on 2026-06-26
200
Participants Needed
2
Research Sites
82 weeks
Total Duration
Researchers are studying the effects of high-frequency electrical current transfer, called TECAR, on pain and functional movement in people with musculoskeletal injuries or pain. The study aims to compare immediate and long-term outcomes of TECAR therapy against transcutaneous electrical nerve stimulation TENS and a control group. The trial includes individuals with acute hamstring strain or low back pain and those with chronic low back pain, assessing how these treatments may impact pain and movement over time. Participants are assigned randomly to one of three groups TECAR therapy using a device delivering 0.5 MHz current at 40-60% intensity, TENS therapy with 80 Hz electrical stimulation, or a control group receiving no active electrical treatment. The acute phase involves a single 20-minute session, with outcome measurements before and up to 48 hours after. The chronic phase includes 10 sessions over about three weeks, with follow-up assessments at 3 and 6 months. These phases allow evaluation of both short-term and lasting effects of the therapies. During the study, participants will undergo various tests including pain rating scales, flexibility and functional movement tests such as sit and reach, straight leg raising, and the Oswestry Disability Index. Assessments occur at multiple time points before and after treatments to track changes. Researchers will use statistical methods to analyze differences between groups over time. The study lasts several months for chronic participants, with close monitoring of pain and muscle function throughout.
CONDITIONS
High Frequency RF Current Effects on Muscle Pain and Function
E
Eleftherios Kellis, Ph.D.
A
Anna Kellis, MSc
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Aristotle University Of Thessaloniki
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 2 days
Participants receive a single 20-minute session of either TECAR therapy, TENS therapy, or no active treatment for acute hamstring strain or acute low back pain. Outcome measures are taken before treatment and up to 48 hours afterward.
Assessments at baseline, immediately after treatment, 24 hours, and 48 hours post-treatment
Duration - Approximately 3 weeks treatment plus 6 months follow-up
Participants with chronic hamstring injury or low back pain receive 10 treatment sessions over about 3 weeks, with TECAR, TENS, or no active intervention. Outcome measures are collected before treatment, immediately after, and during follow-ups at 3 and 6 months.
Regular assessments before treatment, after treatment, and at 3 and 6 months follow-up
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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Lead Sponsor