| P50 | author | Kerry Woolfall | Q56508033 |
| | Louise Madden | Q58131085 |
| P2093 | author name string | B Young | |
| | P R Williamson | |
| | R L Smyth | |
| | V Shilling | |
| | E Sowden | |
| P2860 | cites work | How do parents experience being asked to enter a child in a randomised controlled trial? | Q33409753 |
| | Communication about children's clinical trials as observed and experienced: qualitative study of parents and practitioners | Q33963792 |
| | Assent is not consent. | Q34102608 |
| | Pediatric clinical trial experience: government, child, parent and physician's perspective | Q35612817 |
| | Faith and protection: the construction of hope by parents of children with leukemia and their oncologists | Q35863896 |
| | Comparisons of adolescent and parent willingness to participate in minimal and above-minimal risk pediatric asthma research protocols | Q36012391 |
| | Children's competence for assent and consent: a review of empirical findings | Q36117048 |
| | Children as partners with adults in their medical care | Q36121179 |
| | Involving children with cancer in decision-making about research participation | Q36669850 |
| | Competent children? Minors' consent to health care treatment and research | Q36940227 |
| | Assessment of children's capacity to consent for research: a descriptive qualitative study of researchers' practices. | Q37884279 |
| | Participation in medical research; a systematic review of the understanding and experience of children and adolescents | Q37948377 |
| | Assent for children's participation in research is incoherent and wrong | Q38384538 |
| | Processes in recruitment to randomised controlled trials of medicines for children (RECRUIT): a qualitative study | Q46498288 |
| | Empty ethics: the problem with informed consent | Q47413950 |
| | Child assent and parental permission in pediatric research | Q47661536 |
| | Family patterns of decision-making in pediatric clinical trials | Q48448128 |
| | "My parents decide if I can. I decide if I want to." Children's views on participation in medical research | Q48500862 |
| | Children's consent to research participation: social context and personal experience invalidate fixed cutoff rules | Q48562079 |
| | Accuracy of the MacArthur competence assessment tool for clinical research (MacCAT-CR) for measuring children's competence to consent to clinical research. | Q50617649 |
| | Decision-making by adolescents and parents of children with cancer regarding health research participation. | Q50732271 |
| | Do they understand? (part II): assent of children participating in clinical anesthesia and surgery research. | Q51304562 |
| | Children's competence to consent to medical treatment. | Q51907260 |
| | Harmonization of Ethics Policies in Pediatric Research | Q58376025 |
| | Qualitative research methods in health technology assessment: a review of the literature | Q77907653 |
| | Distributed decision making: the anatomy of decisions-in-action | Q80490849 |
| | The micropolitics of responsibility vis-à-vis autonomy: parental accounts of childhood genetic testing and (non)disclosure | Q80747941 |
| | Regulating trust in pediatric clinical trials | Q81660163 |
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 900-908 | |
| P577 | publication date | 2016-05-02 | |
| P1433 | published in | Child: Care, Health and Development | Q5097678 |
| P1476 | title | Questioning assent: how are children's views included as families make decisions about clinical trials? | |
| P478 | volume | 42 | |