Informed consent, parental awareness, and reasons for participating in a randomised controlled study. - Wikidata - wikimedia - TriplyDB

Informed consent, parental awareness, and reasons for participating in a randomised controlled study.

Informed consent, parental awareness, and reasons for participating in a randomised controlled study.

http://www.wikidata.org/entity/Q35260500

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Motivations of children and their parents to participate in drug research: a systematic review Ethical considerations for informed consent in infertility research: The use of electronic health records Parental comprehension of the benefits/risks of first-line randomised clinical trials in children with solid tumours: a two-stage cross-sectional interview study What motivates British parents to consent for research? A questionnaire study.How do parents experience being asked to enter a child in a randomised controlled trial?Ethical issues at the interface of clinical care and research practice in pediatric oncology: a narrative review of parents' and physicians' experiences.Understanding the African American Research Experience (KAARE): Implications for HIV Prevention.The quality of informed consent: mapping the landscape. A review of empirical data from developing and developed countries Comparing the understanding of subjects receiving a candidate malaria vaccine in the United States and Mali Experiences of families with a child, adolescent, or young adult with neurofibromatosis type 1 and plexiform neurofibroma evaluated for clinical trials participation at the National Cancer Institute.The definition of placebo in the informed consent forms of clinical trials.Challenges to obtaining parental permission for child participation in a school-based waterpipe tobacco smoking prevention intervention in Qatar.Parental recall of anesthesia information: informing the practice of informed consent Clinical trials involving cats: what factors affect owner participation?Reported consent processes and demographics: a substudy of the INSIGHT Strategic Timing of AntiRetroviral Treatment (START) trial.Participants' understanding of informed consent in clinical trials over three decades: systematic review and meta-analysis.Parental involvement in paediatric cancer treatment decisions.Research in general paediatrics.Presumed consent in emergency neonatal research Exploring issues of parental consent to research: a case-study approach.Parental consent in paediatric clinical research.Discussions of cancer clinical trials with the National Cancer Institute's Cancer Information Service Effect of child health status on parents' allowing children to participate in pediatric research Compensation for research related injury.Can patient decision aids help people make good decisions about participating in clinical trials? A study protocol Informing the uninformed: optimizing the consent message using a fractional factorial design Parents' agendas in paediatric clinical trial recruitment are different from researchers' and often remain unvoiced: a qualitative study.A questionnaire on factors influencing children's assent and dissent to non-therapeutic research.Investigating the Experiences of Childhood Cancer Patients and Parents Participating in Optional Nontherapeutic Clinical Research Studies in the UK.Using animation as an information tool to advance health research literacy among minority participants.Perceptions of parents on the participation of their infants in clinical research.Assessing the interest to participate in a dengue vaccine efficacy trial among residents of Puerto Rico.Parental informed consent in pediatric cancer trials: a population-based survey in Germany.Listening to Quackery: Reading John Wesley's Primitive Physic in an Age of Health Care Reform.Satisfying the needs of Japanese cancer patients: a comparative study of detailed and standard informed consent documents.Why substitute decision makers provide or decline consent for ICU research studies: a questionnaire study.Informed consent for pediatric leukemia research: clinician perspectives.Clinical trials in neonates: How to optimise informed consent and decision making? A European Delphi survey of parent representatives and clinicians.Parental Perceptions About Informed Consent/Assent in Pediatric Research in Jordan Anticipatory guidance to improve informed consent: a new application of the concept

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P2860

Informed consent, parental awareness, and reasons for participating in a randomised controlled study.

http://www.wikidata.org/entity/Q35260500

description

1998 nî lūn-bûn

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1998 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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1998 թվականի օգոստոսին հրատարակված գիտական հոդված

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1998年の論文

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1998年論文

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1998年論文

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1998年論文

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1998年論文

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1998年論文

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1998年论文

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Archives of Disease in Childhood

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Informed consent, parental awa ...... a randomised controlled study.

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Derksen-Lubsen G

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Moll HA

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Steyerberg EW

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Suur MH

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Tjiang GC

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P2860

Risks and benefits of paracetamol antipyresis in young children with fever of presumed viral origin.

Questionnaire design.

Sociodemographic and motivational characteristics of parents who volunteer their children for clinical research: a controlled study.

Informed consent: study of quality of information given to participants in a clinical trial.

How to do it. Get patients' consent to enter clinical trials

Attitudes toward clinical trials among patients and the public.

Effect of acetaminophen and of low intermittent doses of diazepam on prevention of recurrences of febrile seizures.

A controlled trial of diazepam administered during febrile illnesses to prevent recurrence of febrile seizures.

Parental reactions to a child's first febrile convulsion. A follow-up investigation.

Intermittent prophylaxis in febrile convulsions: diazepam or valproic acid?

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10.1136/ADC.79.2.120

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2

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79

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13488064

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9797591

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informed consent

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1717659

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