Search results for "controlled"

showing 10 items of 2729 documents

Process evaluation of a complex workplace intervention to prevent musculoskeletal pain in nursing staff: results from INTEVAL_Spain

2021

Abstract Background INTEVAL_Spain was a complex workplace intervention to prevent and manage musculoskeletal pain among nursing staff. Process evaluations can be especially useful for complex and multifaceted interventions through identifying the success or failure factors of an intervention to improve the intervention implementation. Objectives This study performed a process evaluation of INTEVAL_Spain and aimed to examine whether the intervention was conducted according to the protocol, to investigate the fulfilment of expectations and the satisfaction of workers. Methods The intervention was a two-armed cluster randomized controlled trial and lasted 1 year. The process evaluation include…

medicine.medical_specialtyRT1-120Psychological interventionSalut en el treballNursingCluster randomized controlled trialCase managementlaw.inventionRandomized controlled trialNursinglawMediterranean dietIntervention (counseling)MedicineNursing managementNordic walkingGeneral Nursingbusiness.industryResearchNursing researchHuman factors and ergonomicsParticipatory ergonomicsPhysical therapyHealth promotionParticipatoryErgonomicsbusinessMindfulnessQualitative researchBMC Nursing
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Effects of a workplace physical exercise intervention on the intensity of low back symptoms in office workers: A cluster randomized controlled cross-…

2006

Objectives. The purpose of the study was to examine the effects of a workplace physical exercise intervention on the intensity of low back symptoms. Methods. The study was a cluster randomized controlled trial with department (n = 4) as the unit of randomization. The subjects were office workers [(n = 36), mean age 47.1 (SD 8.4) years] who self-reported low back symptoms, which restricted their daily activities during the last 12 months. Low back symptoms were measured using the Borg CR10 scale. The cross-over design consisted of one intervention period of light resistance training and guidance and no training and no guidance of 15 weeks duration. Statistical analyses were based on linear m…

medicine.medical_specialtyRandomizationActivities of daily livingbusiness.industryRehabilitationPhysical Therapy Sports Therapy and RehabilitationPhysical exerciseDisease clusterCrossover studyIntensity (physics)law.inventionPhysical medicine and rehabilitationRandomized controlled triallawIntervention (counseling)Physical therapymedicineOrthopedics and Sports MedicinebusinessJournal of Back and Musculoskeletal Rehabilitation
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Reducing the initial number of rituximab maintenance-therapy infusions for ANCA-associated vasculitides: randomized-trial post-hoc analysis

2020

AbstractObjectiveThe randomized, controlled MAINRITSAN2 trial was designed to compare the capacity of an individually tailored therapy [randomization day 0 (D0)], with reinfusion only when CD19+ lymphocytes or ANCA had reappeared, or if the latter’s titre rose markedly, with that of five fixed-schedule 500-mg rituximab infusions [D0 + D14, then months (M) 6, 12 and 18] to maintain ANCA-associated vasculitis (AAV) remissions. Relapse rates did not differ at M28. This ancillary study was undertaken to evaluate the effect of omitting the D14 rituximab infusion on AAV relapse rates at M12.MethodsMAINRITSAN2 trial data were subjected to post-hoc analyses of M3, M6, M9 and M12 relapse-free surviv…

medicine.medical_specialtyRandomizationAntigens CD19Anti-Neutrophil Cytoplasmic Antibody-Associated VasculitisGastroenterologyDisease-Free SurvivalDrug Administration ScheduleAntibodies Antineutrophil CytoplasmicMaintenance Chemotherapylaw.invention03 medical and health sciences0302 clinical medicineRheumatologyMaintenance therapyRandomized controlled triallawInternal medicinePost-hoc analysismedicineHumansPharmacology (medical)030212 general & internal medicineSurvival rate030203 arthritis & rheumatologybusiness.industrymedicine.diseaseAntirheumatic AgentsRituximabRituximabMicroscopic polyangiitisGranulomatosis with polyangiitisbusinessmedicine.drugRheumatology
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Analgesics for Dental Implants: A Systematic Review

2021

Postsurgical pain is commonly associated with dental and oral surgery, and the use of analgesics has been investigated in the management of postoperative pain. This systematic review summarizes available evidence on analgesics used to manage dental implant surgery postoperative pain, to identify best therapeutic protocols and knowledge gap. A comprehensive search was conducted including MEDLINE/Pubmed, EMBASE, SCOPUS, clinicaltrials.gov, and the Cochrane Database of Systematic Reviews through May 2020. Only randomized controlled trials were included. PRISMA guidelines were followed, and risk of bias was appraised using Cochrane RoB2 tool. Eleven trials (762 patients overall) were included. …

medicine.medical_specialtyRandomizationOral surgerymedicine.medical_treatmentMEDLINEPlacebolaw.invention03 medical and health sciences0302 clinical medicineRandomized controlled trialsystematic reviewlawMedicinePharmacology (medical)painDental implantPharmacologydental implantbusiness.industrylcsh:RM1-950analgesics; dental implant; pain; post-operative pain; systematic review030206 dentistryRescue medicationSystematic reviewpost-operative painlcsh:Therapeutics. PharmacologyPhysical therapyanalgesicsbusiness030217 neurology & neurosurgeryFrontiers in Pharmacology
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Randomized controlled study of a mandibular advancement appliance for the treatment of obstructive sleep apnea in children: A pilot study

2015

Background: The current limited evidence may be suggestive that mandibular advancement appliance (MAAs) result in improvements in AHI scores, but it is not possible to conclude that MAAs are effective to treat paediatric OSA. There are significant weaknesses in the existing evidence due primarily to absence of control groups, small sample sizes, lack of randomization and short-term results. Aim: the objective of the present study was to evaluate MAAs in children with OSA. Material and Methods: Children presenting an apnea-hypopnea index (AHI) greater than or equal to one event per hour were considered to be apneic. This group of children with AHI greater than or equal to one was randomly di…

medicine.medical_specialtyRandomizationPolysomnographylcsh:BF1-990Neuroscience (miscellaneous)MEDLINEMedicine (miscellaneous)Odontologíalcsh:Consciousness. CognitionPilot ProjectsPolysomnographylaw.inventionDental OcclusionBehavioral Neuroscience03 medical and health sciences0302 clinical medicineRandomized controlled trialstomatognathic systemlawotorhinolaryngologic diseasesmedicineHumansChildGeneral DentistrySleep Apnea ObstructiveOral Medicine and Pathologymedicine.diagnostic_testbusiness.industryDental occlusionResearchSleep apneaSmall sample:CIENCIAS MÉDICAS [UNESCO]lcsh:BF309-499medicine.diseaseCiencias de la saludnervous system diseasesrespiratory tract diseasesObstructive sleep apnealcsh:PsychologyTreatment Outcome030228 respiratory systemOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASPhysical therapySurgerybusinessMandibular Advancement030217 neurology & neurosurgeryMedicina Oral, Patología Oral y Cirugía Bucal
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Transesophageal Echocardiography - Dysphagia Risk in Acute Stroke (TEDRAS): a prospective, blind, randomized and controlled clinical trial.

2020

BACKGROUND AND PURPOSE Dysphagia is common in acute stroke and leads to worse overall outcome. Transesophageal echocardiography (TEE) is used in the diagnostic evaluation of stroke with regard to its etiology and is a known cause of postoperative dysphagia in cardiac surgery. The prevalence of dysphagia in acute stroke patients undergoing TEE remains unknown. The aim of the Transesophageal Echocardiography - Dysphagia Risk in Acute Stroke (TEDRAS) study was to assess the influence of TEE on swallowing among patients who have experienced acute stroke. METHODS The TEDRAS study was a prospective, blind, randomized, controlled trial that included two groups of patients with acute stroke. Simple…

medicine.medical_specialtyRandomizationlaw.invention03 medical and health sciences0302 clinical medicineRandomized controlled trialSwallowinglawMedicineHumans030212 general & internal medicineProspective StudiesStrokebusiness.industrymedicine.diseaseDysphagiaCardiac surgeryDeglutitionClinical trialStrokeNeurologyAnesthesiaEtiologyNeurology (clinical)medicine.symptombusinessDeglutition Disordershuman activities030217 neurology & neurosurgeryEchocardiography TransesophagealEuropean journal of neurologyReferences
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A Large-Scale Trial Testing the Intensità of CYTOreductive Therapy to prevent Cardiovascular Events in Patients with Polycythemia Vera (CYTO-PV trial…

2012

Abstract Abstract 4 Introduction Current treatment recommendations in polycythemia vera (PV) have emphasized to maintain the hematocrit (HCT) values <0.45 based on hemorrheological notions, results of a few small observational retrospective studies and consensus of experts. However, post-hoc analysis of two large randomized clinical trials (namely PVSG-1 and ECLAP) failed to show a different incidence of major thrombosis when HCT levels were kept in the range between 0.40 and 0.50. So far, no randomized clinical trial has provided evidence-based data assessing the usefulness of tight HCT control in reducing thrombosis. Thus, uncertainty of the optimal HCT target exists in clinical practi…

medicine.medical_specialtyRandomizationmedicine.diagnostic_testbusiness.industrySurrogate endpointImmunologyWarfarinCell BiologyHematologyPhlebotomyHematocritmedicine.diseaseBiochemistrylaw.inventionPolycythemia veraRandomized controlled triallawConcomitantInternal medicineMedicinebusinessmedicine.drug
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PROSPECTIVE, RANDOMIZED, CROSSOVER COMPARISON OF SUBLINGUAL APOMORPHINE (3 mg) WITH ORAL SILDENAFIL (50 mg) FOR MALE ERECTILE DYSFUNCTION

2004

Abstract: Purpose: We established the efficacy and safety of sublingual apomorphine compared with oral sildenafil. in comparable groups of patients with erectile dysfunction (ED). Materials and Methods: This prospective, randomized, crossover study included 77 heterosexual men with ED of various etiologies and severities. A total of 62 men were randomized but only 34 were evaluable for efficacy and tolerability. The study started with a run-in period of 2 to 4 weeks. The first 4 weeks of treatment were followed by a washout period of 4 weeks, after which patients changed to the alternate treatment for an additional 4-week period. The sequence of the 2 treatments was established by a randomi…

medicine.medical_specialtyRandomizationmedicine.drug_mechanism_of_actionSildenafilUrologyUrologyPenis Impotence Apomorphine SildenafilSildenafil 50 MGlaw.inventionSettore MED/24 - Urologiachemistry.chemical_compoundRandomized controlled triallawmedicineProspective cohort studybusiness.industryMale erectile dysfunctionmedicine.diseaseCrossover studyrespiratory tract diseasesApomorphineErectile dysfunctionmedicine.anatomical_structureTolerabilitychemistryAnesthesiacardiovascular systemSexual functionbusinessPhosphodiesterase 5 inhibitorPenismedicine.drug
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Is arthrocentesis of temporomandibular joint with corticosteroids beneficial? A systematic review

2018

Background Temporomandibular disorders (TMDs) are musculoskeletal conditions that can inhibit the normal function of temporomandibular joints (TMJs) and affect the patient’s quality of life, negatively. Arthrocentesis (AC) is a minimally invasive surgical procedure used for treating TMDs. The aim of present paper is to evaluate the advantages of administrating corticosteroid (CS) during AC by reviewing high quality released articles. Material and Methods Searching on Cochrane Library, Web of Science, Google Scholar, PubMed, ProQuest, and Scopus databases were performed with focusing on proper key words. Related titles and abstracts, up to December 2017, were screened and selected based on i…

medicine.medical_specialtyRandomizationmedicine.medical_treatmentMEDLINEPain reliefReviewCochrane Librarylaw.invention03 medical and health sciences0302 clinical medicineRandomized controlled trialQuality of lifestomatognathic systemlawmedicineHumans030212 general & internal medicineGlucocorticoidsGeneral DentistryRandomized Controlled Trials as Topicbusiness.industryArthrocentesis030206 dentistryTemporomandibular Joint Disorders:CIENCIAS MÉDICAS [UNESCO]Combined Modality TherapyTemporomandibular jointstomatognathic diseasesmedicine.anatomical_structureOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASPhysical therapySurgeryOral SurgerybusinessArthrocentesis
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Effects of exercise programs on physical function and activity levels in patients undergoing hemodialysis: a randomized controlled trial

2021

Background There are still many barriers when implementing exercise routines within daily dialysis care, even though benefits are well-known. Developing cost-effective strategies is necessary to overcome these barriers and include exercise as a complementary therapy in dialysis. Aim To compare several exercise programs on hemodialysis patient's functional capacity and health-related quality of life. Design This study was a 16-week follow-up, two-parallel group trial with balanced randomization. Setting Participants in this study belonged to a private hospitalized care center. Population Referred sample of 71 patients that suffered end-stage chronic kidney disease who underwent hemodialysis …

medicine.medical_specialtyRandomizationmedicine.medical_treatmentPopulationPhysical Therapy Sports Therapy and Rehabilitationlaw.inventionQuality of life (healthcare)Randomized controlled trialRenal DialysislawHumansMedicineeducationExerciseDialysisAgededucation.field_of_studyRehabilitationbusiness.industryRehabilitationmedicine.diseaseExercise TherapyHemodialysis Units HospitalQuality of LifePhysical therapyHemodialysisbusinessKidney diseaseEuropean Journal of Physical and Rehabilitation Medicine
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