Clinical trials: VALİDİTY
Healthy
Validation of Smart Garments for Gait Classification
The aim of this study is therefore to validate Myant SKIIN garments for the purpose of gait and balance assessment. To achieve this, we recruit young healthy adults from the University of Waterloo to wear Skiin products (see Fig.
- Trial name
- NCT05898555
- Testing
- Skiin garment and pods
- Where
- Canada
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Myant Medical Corp.
Conscious Sedation Failure During Procedure
Remifentanil Effect-site Prediction by Algometry
This study validates the pharmacodynamic analgesic predictions (effect) given by Minto's remifentanil pharmacokinetic and dynamic model in conscious sedation.
- Trial name
- NCT05115578
- Testing
- Remifentanil 1 MG Injection [Ultiva], Midazolam 1 MG/ML Prefilled Syringe, Saline solution
- Where
- Spain
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Hospital Universitari Vall d'Hebron Research Institute
Minimally Conscious State, Vegetative State
Reliability and Validity of the NCS (NCS-R)-Chinese Version
The aim of this study was to translate the NCS from English into Chinese and determine the validity of this Chinese version.
- Trial name
- NCT03494218
- Testing
- Nociception Coma Scale (NCS)
- Where
- China
- Volunteers
- 62 people
- Sponsor
- Hangzhou Normal University
Lupus Erythematosus, Systemic
CD19-Directed CAR-T Cell Therapy in Refractory Systemic Lupus Erythematosus
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease in which the immune system mistakenly attacks the body's own tissues and organs.
- Trial name
- CLEVER-SLE (NCT07659704)
- Testing
- Autologous CD19-Directed CAR-T Cells Manufactured at Ribeirão Preto Blood Center
- Where
- 2 sites in Brazil
- Volunteers
- 16 people
- Sponsor
- University of Sao Paulo
Cubital Tunnel Syndrome, Peroneal Nerve Entrapment
Mechanomyography for Predictor of Prognosis in CuTS and PND Patients
The study will be a non-blinded two cohort design consisting only of symptomatic patients with CuTS or compressive peroneal neuropathy or in need of peroneal nerve decompression. The first cohort will be - patients with CuTS.
- Trial name
- NCT04322448
- Testing
- Mechanomyography (MMG)
- Where
- 2 sites in United States
- Volunteers
- 23 people
- Sponsor
- Washington University School of Medicine
Diagnosis, Dual (Psychiatry)
Dual Integrated Attention Program (DAIP) in People With Severe Dual Diagnosis
Aim: validate a Dual Integrated Attention Program (D-AIP) for mental health nursing in people with Severe Dual Diagnosis admitted to a psychiatric hospitalization unit Design: Randomized Controlled Trial.
- Trial name
- PAI-D (NCT04442776)
- Testing
- D-AIP
- Volunteers
- 86 people
- Sponsor
- Cardenal Herrera University
Lateral Sclerosis
Validation of the French Version of the Primary Lateral Sclerosis Functioning Rating Scale (PLSFRS)
This is a national, multicentric, prospective, descriptive study evaluating the psychometric properties of the French version PLSFRS scale
- Trial name
- FRENPRILS (NCT06878235)
- Testing
- Assessment of the functional status
- Where
- 7 sites in France
- Volunteers
- 80 people
- Sponsor
- University Hospital, Tours
Disc Herniations, Disc Herniation, Lumbar
Smartwatch Accuracy for Measuring Vitals and Anxiety Before Disc Surgery
This study aims to verify the accuracy of blood pressure, heart rate, blood oxygen saturation, anxiety level, and sleep cycle data measurements obtained from Samsung smartwatches compared to the currently accepted method used in…
- Conditions
- Disc Herniations, Disc Herniation, Lumbar, Cervical Disc Herniation, Preoperative Anxiety Score
- Trial name
- NCT07322523
- Where
- Turkey (Türkiye)
- Volunteers
- 60 people
- Sponsor
- Halil Kalaycı
Anastomotic Leak, Colorectal Surgery
Early Diagnosis of Anastomotic Leakage After Colorectal Surgery: Italian ColoRectal Anastomotic Leakage Study Group.
Prospective evaluation of early diagnosis of anastomotic leak after colorectal resection through evaluation of Dutch leakage score, serum C-reactive protein and serum Procalcitonin
- Trial name
- iCral (NCT03560180)
- Testing
- Dutch score, Serum C-reactive Protein, serum Procalcitonin
- Where
- 18 sites in Italy
- Volunteers
- 1,131 people
- Sponsor
- Ospedale C & G Mazzoni
Funcional Status, Return to Work
Machine Learning Model for Predicting Recovery After Critical Illness
This study aims to develop and test an artificial intelligence (AI) model to predict long-term functional status and return to work after critical illness.
- Conditions
- Funcional Status, Return to Work, Predictive Learning Models
- Trial name
- NCT07616388
- Testing
- No interventions were performed.
- Where
- Brazil
- Volunteers
- 2,016 people
- Sponsor
- Hospital de Clinicas de Porto Alegre
Surgery Requiring Spinal Anesthesia
Validation of Phase Lag Entropy(PLE) as an Indicator of Depth of Sedation in Patients Undergoing Spinal Anesthesia
For verifying the phase lag entropy as the tool for measurement of level of consciousness, the investigators compared phase lag entropy to bispectral index.
- Trial name
- NCT03319004
- Testing
- apply phase lag entropy sensor
- Where
- South Korea
- Volunteers
- 27 people
- Sponsor
- Gangnam Severance Hospital
Dementia
Cross-cultural Adaptation of the Greek Version of Disability Assessment for Dementia
The main purpose of this study is primarily the translation and cross-cultural adaptation into Greek and then the investigation of validity and reliability in the Greek target population.
- Trial name
- DAD-Gr (NCT05850715)
- Testing
- Disability Assessment for Dementia (DAD)
- Where
- Greece
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- University of Thessaly
Hospitalized Patients, Physical Inactivity
SHIFT-Hospital in Motion (Hospital Implementation Study)
The goal of this monocentric observational study involving hospitalised patients is to assess the integration of activity sensors into routine clinical practice.
- Trial name
- NCT06784011
- Where
- Switzerland
- Volunteers
- 19 people
- Sponsor
- University Hospital, Basel, Switzerland
Chronic Pain, Opioid Misuse
French Version of POMI Scale
French translation and validation of the Prescription Opioid Misuse Index scale (POMI), a brief questionnaire to assess opioid prescription misuse.
- Trial name
- POMI (NCT04979364)
- Volunteers
- 154 people
- Sponsor
- University Hospital, Clermont-Ferrand
Healthy
VALIDITY AND RELIABILITY OF THE 6-MINUTES WALKING TEST EVALUATED BY FEETME® INSOLES
Currently, the guidelines for performing the 6MWT established by the American Thoracic Society and the European Respiratory Society (ATS/ERS) recommend the use of an indoor or outdoor corridor with a 30 m flat surface (6MWT30)…
- Trial name
- ValiFeet6 (NCT05536687)
- Testing
- FeetMe
- Where
- France
- Volunteers
- 45 people, healthy volunteers welcome
- Sponsor
- FeetMe
Osteoporosis, Fracture
Develop and Validate Ultrasonic Device for Osteoporotic Fracture Risk Assessment
Study to demonstrate that the Bone UltraSonic Scanner (BUSS) can aid in detection of osteoporosis and predict prevalent osteoporotic fractures.
- Conditions
- Osteoporosis, Fracture, Aging
- Trial name
- BUSS03 (NCT01123421)
- Where
- United States
- Volunteers
- 113 people
- Sponsor
- Artann Laboratories
Brain Neoplasms, Cerebral Aneurysm
Clinical Trial for the Validation of AR Based Neuronavigation System
The goal of this clinical trial is to test augmented reality (AR) based neuronavigation system in surgeries for patients of brain neoplasm or cerebral vascular disease.
- Conditions
- Brain Neoplasms, Cerebral Aneurysm, Cerebral Arteriovenous Malformation, Navigation, Spatial
- Trial name
- NCT05776706
- Testing
- AR-based navigation
- Where
- South Korea
- Volunteers
- 80 people
- Sponsor
- Seoul National University Hospital
Sleep Apnea, Sleep-Disordered Breathing
Alice PDx User/Validation Extended Trial
The objective of this study is to test the usability of the Alice PDx device by both the end user (patient/participant) and the sleep technician.
- Trial name
- NCT00841906
- Testing
- Alice PDx with only written instructions, Alice PDx with written and verbal instructions
- Where
- 2 sites in United States
- Volunteers
- 32 people
- Sponsor
- Philips Respironics
Prostate Cancer, Prostate Adenocarcinoma
ARCTIC: Liquid Biomarkers in the Prospective Androgen Receptor Signaling Inhibitors (ARSI) Resistance Clinical Trials
This study will follow men with metastatic castration resistant prostate cancer throughout their standard of care treatment for their disease to determine if the presence of different genes or proteins can predict which patients…
- Conditions
- Prostate Cancer, Prostate Adenocarcinoma, Prostate Cancer Metastatic, Castration-resistant Prostate Cancer
- Trial name
- ARCTIC (NCT06141993)
- Where
- 3 sites in United States
- Volunteers
- 120 people
- Sponsor
- Duke University
Validation of Vital Signs Measured by a Consumer-grade Smartwatch
Comparing the Garmin Venu 3 / Garmin Venu 4 for Non-Invasive Vital Sign Monitoring to a Hospital-Grade Monitor
This clinical trial evaluates the accuracy of the Garmin Venu 3 / Garmin Venu 4 smartwatch in measuring vital signs (heart rate, respiratory rate, SpO₂) compared to the clinically validated Philips IntelliVue X2.
- Trial name
- GARMIN (NCT07360678)
- Testing
- Garmin Venu 3 or Garmin Venu 4 + Philips Intellivue X2, Smartwatch rating scale questionnaire
- Where
- Belgium
- Volunteers
- 30 people
- Sponsor
- Ziekenhuis Oost-Limburg
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