Written informed consent was obtained from all participants prior to enrolment into the trial. The trial was prospectively registered at the Australian New Zealand Clinical Trial Registry (www.anzctr.org.au; ACTRN12618000221257 with a Universal Trial Number: U1111-1194-6282). One important deviation...
Sample size determination The sample size was determined according to the previous trials using G Power10,11. An effective sample size of 16 subjects in each treatment group would have a power greater than 0.80 (β = 0.2) with an α-level of 0.05, and also have one-sided significance...
In this single window system of plus one admissions, candidates need to submit online application in HSCAP website, In the online application process, you need to submit the SSLC exam grades, Date of Birth, Details of Bonus Points for club activities etc and all other details to secure the...
All patients who participate in the RESPECT study need to give written informed consent prior to the EMR. Ethical approval of the study protocol has been obtained from the accredited Medical Research Ethics Committee (METC) of the region Arnhem-Nijmegen, the Netherlands (reference number 2020–7272...
This trial followed the Declaration of Helsinki Good Clinical Practice guidelines (ICH-GCP) for trial conduct and included an external audit. All trial participants provided written informed consent and were not reimbursed for participating in the trial. The trial protocol was approved by the ...
Exclusion criteria are: age <18 years or >65 years; permanent exclusion from the workforce; inability to understand the Danish language; any serious medical condition; and lack of written informed consent. We plan to randomise 742 participants. Interventions: The experimental intervention is an ...
The inclusion criteria for employees are 1) being aged ≥ 18 years; 2) being able to answer the questionnaires written in Japanese; 3) having access to the Internet and the intervention programs offered online; 4) having a private smartphone available; 5) working at a workplace (or ...
was registered on the Australian New Zealand Clinical Trials Registry (https://www.anzctr.org.au/—Trial Id: ACTRN12619001519145) on November 4, 2019. Each respondent gave written informed consent. All investigations were conducted according to the principles expressed in the Declaration of Helsinki...
All participants provided written informed consent before the performance of any study-specific procedures. Participants were eligible if they were male, aged 18–65 years, weighed 40–90 kg and had a new episode of untreated, rifampicin-susceptible pulmonary TB. All participants were male due...
All patients provided written informed consent before entering the trial and this trial was conducted in accordance with Good Clinical Practice, the ethical principles laid down in the Declaration of Helsinki and applicable regulatory requirements. The full study protocol is available as a supplementary ...