Institutional review boards at all sites approved the study, and all participants provided written informed consent. The study protocol and other forms are available in Supplement 1. Participants and Eligibility Criteria Clinicians Clinicians were recruited from 2 large health care systems in the Pacific...
With patient consent we contacted their GP, and asked them to complete a template. We validated the date of reported first presentation of each symptom, for both exact dates and estimated dates. For exact dates, we asked GPs whether there was a consultation on that particular day, or within...
Intervention Details are in the protocol, which features a recommended template to describe a complex intervention.5,21,22 The multicomponent intervention was codesigned by an 18-member panel to address complex barriers at multiple levels that prevent kidney transplant and living donation.4 The panel ...
Is there a template I can use for my patient portal? Yes! Caspio offers a free, ready-madepatient portal templatethat you can customize to accelerate your digital initiatives. It includes essential patient management features such as a registration form for new patients and dashboards for trackin...
RB, JC, JF, DM, and JM were responsible for recruiting patients, informed consent, collecting samples, and some biomedical analysis. DT, KK, and SW carried out the DNA extractions, PCR, and qPCR analysis. KK, SW and DT were responsible for the data analysis, as well as the writing ...
A node can leave the network without any consent from the other nodes in the network. Bitcoin is one of the most popular examples that fall under the public and permissionless blockchain. Proof of Work (POW), Proof-of-Stake (POS), and directed acyclic graph (DAG) are some examples of ...
Informed consent to participate in our study was obtained from all participants. No adverse events following the biopsy procedure were reported. Consent for publication All authors confirm their consent for publication. Competing interests Several authors of this publication are members of the Radboudumc...
(PPMI; ppmi-info.org). Following good clinical practices and in accordance with the Declaration of Helsinki guidelines, study subjects and/or authorized representatives gave written informed consent at the time of enrollment for sample collection and completed questionnaires approved by each participating...
We obtained written, informed consent from all participants before they enrolled in the trial. Treatments took place at physiotherapy clinics, general practices, or clinic rooms at a research institute (Neuroscience Research Australia) in Sydney, Australia. One of 2 trial clinicians (A.C.T. and ...
Informed consent for molecular analysis was obtained and the study was approved by the ethical committee of Paris Ile de France II. Genome linkage screening and linkage analysis Genome-wide homozygosity mapping was performed using 250K Affymetrix single-nucleotide polymorphism (SNP) arrays. Data were ...