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112 results for “Informed consent”
SMA-TB Clinical trial: video & electronic informed consent
<p>The first SMA-TB video has been produced aiming a better understanding of SMA-TB Randomized Clinical Trial (RCT) objectives and procedures. This RCT is work package 1 of SMA-TB project. It is entitled <em>"Phase 2b Randomized double-blind, placebo controlled trial to estimate the potential efficacy and safety of two repurposed drugs, acetylsalicylic acid and ibuprofen, for use as adjunct therapy added to, and compared with, the standard WHO recommended TB regimen (SMA-TB)”, </em>and is registered in ClinicalTrials.gov data under identifier NCT04575519</p> <p>This video has been conceptualized as an e-informed consent for TB patients aiming their participation in SMA-TB CTs in Georgia and South Africa, as well as for anyone wanting to learn about the SMA-TB CT. The video explains in a very comprehensive way the rationale of SMA-TB concept, how the CT will be performed, what is expected from the patient, which are potential benefits, as well as side effects. The message is produced both in English and in Georgian.</p>
Webinar- Rethinking informed consent
<p>Recordings on the <a href="https://i-consentproject.eu/experts-views-on-digitalisation-and-policy-developments-of-clinical-research/">online workshop</a> organized by AND-CG and held on 26 March 2020.</p> <p>The workshop counted with the participation of seven experts (four external and three members of the i-CONSENT consotium) who conducted <a href="https://i-consentproject.eu/i-consent-virtual-workshop-rethinking-informed-consent-emerging-challenges-in-the-digital-era/">presentations on the impact of technology and digitalisation</a> on IC processes in clinical trials.</p>
Questionnaire on gender and age-related peculiarities in informed consent to clinical trials – National legislation
<p>European experts from the six selected countries (Germany, Spain, Austria, France, Italy, and United Kingdom) included in research done within task 1.3 (Ethical and legal review of gender and age-related issues associated with the acquisition of informed consent) participated in a survey on gender and age-related peculiarities in informed consent to clinical trials within national legislations.</p> <p>Experts were selected for their high-level scientific expertise in the fields relevant to the objectives of task 1.3. A short questionnaire on “Gender and age-related peculiarities in informed consent to clinical trials within national legislations" has been prepared and circulated to contact experts. This questionnaire was meant to identify the legal review process and collect up-to-date data. It was structured in 10 queries, exclusively aimed at obtaining hard law and soft law information pertaining to the topics addressed in task 1.3.</p>
Patient Representatives' Perspective on Informed Consent: Nominal Group Data
<p>For Task 1.6 of the i-CONSENT project, a one day workshop was organised with nine attendees from eight European patient groups. During the workshop, Nominal Group Technique (NGT) was used to explore issues that were considered pertinent within each of the four themes (comprehension, patient expectations, gender and assent), and to reach a consensus in terms of their significance. During this exercise, the workshop facilitator presented a short introduction to the theme, before each participant was given sticky notes and instructed to write down as many individual issues as possible using a separate sticky note for each idea. There was no limit to the number of ideas the participants could generate. This stage was conducted in silence and repeated for each of the four themes. The attached documents include the list of all the ideas collected on sticky notes notes during this stage and the ranking of the items done by the participants.</p>
SURVEY ON INFORMED CONSENT (IC) MANAGEMENT DURING THE PANDEMIC
<p>Data obtained through a survey with representatives of different Spanish biobanks about the adaptations done by some of the biobanks of the Spanish Biobank Network to manage the Informed Consent process during the COVID-19 pandemic</p>
Worskshop: a Neurobioethical Perspective on Informed Consent (4 videos)
<p>UNESCO Chair presents is first one-day workshop: <em><strong>A Neurobioethical Perspective on Informed Consent </strong></em>within the <a href="http://i-consentproject.eu/">i-Consent</a> project which works on improving guidelines for Informed Consent, including vulnerable populations, under a gender perspective.</p> <p>During the workshop ten experts on the field will discuss:</p> <p>1. What would be the consequences of reaching an identification of the neural correlates of the ordinary decision-making process behind the notion of informed consent?</p> <p>2. Cognitive and other enhancers might paradoxically create new groups of vulnerable populations (i.e. soldiers): what are the implications of this awareness in relation to informed consent?</p> <p>3. Cultural biases have been proven to exist also at a neuronal level, in which way should we filter such an information in relation to informed consent?</p>
Improving Informed Consent for Palliative Chemotherapy
ClinicalTrials.gov study NCT02282722. IPD Sharing: YES. Countries: 1. Publications: 6.
Improving Informed Consent in Pediatric Endoscopy
ClinicalTrials.gov study NCT00899392. IPD Sharing: Not stated. Countries: 1. Publications: 5.
Easy-to-Read Informed Consent (ETRIC) for Hematopoietic Cell Transplantation Clinical Trials (BMT CTN 1205)
ClinicalTrials.gov study NCT02081248. IPD Sharing: YES. Countries: 1. Publications: 1.
The Effect of Electronic Informed Consent Information (EICI) on Residual Newborn Specimen Research
ClinicalTrials.gov study NCT03141307. IPD Sharing: NO. Countries: 1. Publications: 4.
Decisional Capacity and Informed Consent in Fragile X Syndrome
ClinicalTrials.gov study NCT02465931. IPD Sharing: NO. Countries: 1. Publications: 2.
Health Literacy Intervention for Informed Consent of Cancer Patients Considering Clinical Trial Participation
ClinicalTrials.gov study NCT01964222. IPD Sharing: Not stated. Countries: 1. Publications: 19.
Educational CD-ROM Compared With Standard Informed Consent for Patients With Colorectal Cancer or a Family History of Colorectal Cancer
ClinicalTrials.gov study NCT00450424. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Protocol, case report(s), ethics approvals, informed consent, inclusion and exclusion criteria underlying: The effect of morning versus evening administration of empagliflozin on its pharmacokinetics and pharmacodynamics characteristics in healthy adults: a two-way crossover, non-randomised trial
Open the record for dataset details and reuse information.
Health sciences librarians’ awareness and incorporation of informed consent standards for medical image publication: A preliminary study
Open the record for dataset details and reuse information.
A pre-post implementation survey of a multi-component intervention to improve informed consent for caesarean section in Southern Malawi
<p>Objective Surgical informed consent is essential prior to caesarean section, but potentially compromised by insufficient communication. We assessed the association between a multi-component intervention and women's recollection of information pertaining to informed consent for caesarean section in a low-resource setting, thereby contributing to respectful maternity care. Design Pre-post implementation survey, conducted from January to June 2018, surveying women prior to discharge. Setting Rural 150-bed mission hospital in Southern Malawi. Participants A total of 160 postoperative women were included: 80 pre- and 80 post-implementation. Intervention Based on observed deficiencies and input from local stakeholders a multi-component intervention was developed, consisting of a standardised checklist, wall poster with a six-step guide and on-the-job communication training for health workers. Primary and secondary outcome measures Individual components of informed consent were: indication, explanation of procedure, common complications, implications for future pregnancies and verbal enquiry of consent, which were compared pre- and post-intervention using χ2 test. Generalized linear models were used to analyse incompleteness scores and recollection of the informed consent process. Results The proportion of women who recollected being informed about procedure-related risks increased from 25/80 to 47/80 (OR 3.13 [95% Confidence Interval 1.64-6.00]). Recollection of an explanation of the procedure changed from 44/80 to 55/80 (OR 1.80[0.94-3.44]), implications for future pregnancy from 25/80 to 47/80 (1.69[0.89-3.20]) and of consent enquiry from 67/80 to 73/80 (OR 2.02 [0.73-5.37]). After controlling for other variables, incompleteness scores post-intervention were 26% lower (Exp(β)=0.74; 95% CI 0.57 – 0.96). Recollection of common complications increased by 29% (Exp(β)=1.29; 95% CI 1.01 – 1.64). Recollection of the correct indication did not differ significantly. Conclusion Recollection of informed consent for caesarean section changed significantly in the post-intervention group. Obtaining informed consent for caesarean section is one of the essential components of respectful maternity care.</p>
APPENDIX L - Workshop Attendance Sheet and Informed Consent Form
<p>APPENDIX L - Workshop Attendance Sheet and Informed Consent Form for Memoryscapes in Recto-spection: Visualizing Avenida, Recto, and Carriedo, Manila as Virtual Memoryscapes through immersive mobile technologies and digital heritage interpretation. Thesis Adviser: Dr. Cathe Desiree S. Nadal, Ph. D.</p>
Subject Information and Consent Form F1J-US-HMCB Duloxetine Once-Daily Dosing Versus Placebo in Patients With Major Depression and Pain
ClinicalTrials.gov study NCT00036335. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Improving Informed Consent for Cleft Palate Repair
ClinicalTrials.gov study NCT02595307. IPD Sharing: NO. Countries: 1. Publications: 7.
Telemedicine's Utility for Augmenting Clinical Trials and Informed Consent TACTIC
ClinicalTrials.gov study NCT00390286. IPD Sharing: Not stated. Countries: 1. Publications: 7.
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OpenNeuro
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