Introduction to Double Blind Sham Controlled
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A randomized double-blind sham-controlled study of tDCS was carried out.
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One presentation shows that the NFT “package” significantly reduced over time symptoms in children with ADHD in a large-scale double-blind sham-controlled study.
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Here we present the first double-blind sham-controlled trial evidence of the efficacy and safety of nVNS in the treatment of gait and motor function in patients with PD.
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METHODS
Fifty male forensic patients with a substance dependence were tested in a double-blind sham-controlled randomized study.
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STUDY DESIGN
The prospective randomised double-blind sham-controlled study aimed to determine the efficacy of WBC on cognitive functioning and biological mechanisms.
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This is a double-blind sham-controlled clinical trial.
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Sixty-eight participants received anodal high definition-transcranial direct current stimulation (HD-tDCS) to focally enhance dlPFC or PPC in a double-blind sham-controlled design.
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In the present double-blind sham-controlled within-subject study, we applied bifrontal transcranial alternating current stimulation (tACS) at the theta frequency (5 Hz) on eighteen healthy volunteers during a gambling task.
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STUDY LAYOUT
Prospective randomized double-blind Sham-controlled study.
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Methods This is a double-blind sham-controlled clinical trial.
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Aim:
The purpose of this double-blind sham-controlled trial was to explore the benefit of BrainQ’s novel and non-invasive, artificial intelligence-powered, frequency-tuned ELF-EMF treatment (BQ) in improving upper extremity motor function (UEMF) in a sub-acute ischemic stroke population.
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Methods: This double-blind sham-controlled study involved 28 healthy adults, between 18 and 30 years.
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Methods: Thirty patients suffering from CDH were enrolled in this randomized double-blind sham-controlled trial and randomly allocated to two groups of 15 patients each.
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In a randomized double-blind sham-controlled crossover trial, 45 MDD patients received aiTBS applied to the left dorsolateral prefrontal cortex (Trial registration: http://clinicaltrials.
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This study is a pilot randomized double-blind sham-controlled trial to evaluate the efficacy of ts-DCS on central neuropathic pain in MS patients.
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Design: Double-blind sham-controlled study.
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The authors examined the therapeutic effect of dTMS in a multicenter double-blind sham-controlled study.
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Research Design: In this randomized double-blind sham-controlled crossover trial, we included 10 patients (49 ± 22 years, 7 ± 13 months since injury, 4 unresponsive wakefulness syndrome, 6 minimally conscious state, 5 traumatic etiologies).
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The aim of this randomized double-blind sham-controlled study is to investigate the short-term effect of rMV on motor recovery in acute stroke patients.
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MATERIALS & METHODS
A total of 16 women with CPP participated in the present double-blind sham-controlled cross-over study.
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METHODS AND RESULTS
Reducing Acute Kidney Injury (REDUCE-AKI) was a single-centre, prospective, randomized, double-blind sham-controlled clinical trial, designed to examine the effect of an automated matched saline infusion with urine output for the prevention of AKI in patients undergoing TAVI.
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Patients and methods A randomized double-blind sham-controlled cross-over design evaluated enhanced PNE (ePNE) using tined quadripolar electrode leads over 6 weeks.
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Methods: The study was a 4-week, randomized, double-blind sham-controlled trial.
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The goal of this double-blind sham-controlled randomized trial was to examine the efficacy of a rolling group MBRP treatment combined with tDCS among individuals interested in reducing their drinking.
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In this double-blind sham-controlled study, corticospinal excitability changes induced in leg M1 of both hemispheres by anodal (2 mA for 20 minutes) or sham tDCS (for 20 min) over the vertex were evaluated.
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