Because of the difficulty of obtaining
written informed consent from each parent, the approved procedure for obtaining consent was such that head teachers consented on behalf of adolescents whose parents did not return the written information leaflets, indicating no objection to the study and their child's participation.
A research assistant obtained
written informed consent from participating parents / guardians and assent from the youths and then administered the questionnaires in the waiting room of the pediatric and adolescent clinic.
The written informed consent from the caretakers on behalf of the participants under 18 years was also obtained.
If the parent / caregiver is happy to continue, the researcher will obtain
written informed consent from the parent to participate in the study.
All patient material for this study was collected after obtaining
written informed consent from participants and an ethical vote approving the study (Institutional Review Board: Ethics Committee of the Medical Faculty of Heidelberg University, Germany / Ethikkommission der Medizinischen Fakultät Heidelberg) according to ICGC guidelines (www.icgc.org).
Oocytes, cumulus cells and frozen embryos were collected from Stanford Fertility and Reproductive Medicine Center after approval by the Stanford Institutional Review Board (IRB); all samples were obtained with
written informed consent from all participants involved in the study.
Human discarded foreskin tissues were obtained from the Shanghai Children's Center upon the approval from the Ethical Review Board of the Institute of Health Sciences and after obtaining
the written informed consent from parents of the child participants.
Written informed consent from all patients or guardians was required.
Not exact matches
Informed written consent to participate in the HBDP was obtained
from all participants.
The regional ethics committees for medical research approved the study and
written informed consent was obtained
from the women.
The authors state that: «The study was approved by the Institutional Review Boards of our institutions... and
informed written consent was obtained
from the patient.»
The study protocol was approved by the Institutional Review Board of Columbia University, and
written informed consent was obtained
from each subject.
Written informed consent was obtained
from the legal guardians of all patients.
Written informed consent was obtained
from all adult participants and the parents of minors.
Written informed consent was obtained
from the parents of participating children after receiving a full explanation of the study.
Written informed consent was obtained
from all mothers.
Written approval for all somatic derivations and subsequent iPSC generation performed in this study was obtained from the Stanford University Institutional Review Board (IRB protocol 10368) and the Stanford University Stem Cell Research Oversight Committee (SCRO protocol 40), and written informed consent was obtained from each individual parti
Written approval for all somatic derivations and subsequent iPSC generation performed in this study was obtained
from the Stanford University Institutional Review Board (IRB protocol 10368) and the Stanford University Stem Cell Research Oversight Committee (SCRO protocol 40), and
written informed consent was obtained from each individual parti
written informed consent was obtained
from each individual participant.
Written informed consent was obtained
from all subjects, and the study was approved by the Department of Veterans Affairs Medical Center and the University of Minnesota Committee on Human Subjects.
Written informed consent was obtained
from all participants.
Written informed consent was obtained
from all subjects.
Informed written consent was obtained
from each participant.
Written informed consent was obtained
from participants who then underwent health screening including: medical, psychological and sleep history, semistructured clinical psychiatric interview, physical examination, complete blood cell count and comprehensive metabolic panel, urine toxicology, 12 - lead electrocardiogram, and polysomnographic sleep disorders screen.
All subjects followed the same testing protocol and
written informed consent was signed and obtained
from the subject.
Regarding student mental health services under Title IV (21st century Schools)(page 447), no mental health services will be delivered without «prior
written,
informed consent from the parent of each child who is under 18 years of age.»
You may not
inform Y of the result of a test conducted for X without having a specific,
written consent from Jones.
Written informed consent was obtained
from the participants in connection with baseline measures.
Only data
from one parent per family (the parent who was screened and gave
written informed consent) was used in the event both parents participated in the intervention sessions.
All participants provided
written informed consent and agreed to be tested or retested for HIV, and were able to successfully complete interviews in Kinyarwanda (the official language of Rwanda), travel to and
from the research site, and participate in a baseline outpatient visit.
Written informed consent is obtained
from every participant.
Informed consent: Written informed consent received from the
Informed consent:
Written informed consent received from the
informed consent received
from the patient?
Written informed consents were obtained
from parents prior to the screening process (12MMHIS188 approved by MacKay Memorial Hospital Institutional Review Board).
Before participating,
written informed consent was obtained
from their parents or guardians.
Written informed consent was obtained
from all subjects, and the study protocol was approved by the Ethics Committee of Inje University Ilsan Paik Hospital.
Written informed consent was obtained
from all participants before joining the study.
Written informed consent was obtained
from parents before screening as well as during on - site visits and magnetic resonance scans.
Exclusions: no
written informed consent; change in choice or resistance to assessment; residence outside catchment area or transferred
from other inpatient facilities.
Written,
informed consent / assent was obtained
from parents and youths.
Written informed consents were obtained
from all parents or main caregivers of the students.
All parents or guardians provided
written informed consent to participate in the study and were free to withdraw
from the research at any time.
Written informed consent was obtained
from parents.
Written informed consent was obtained
from adolescents and parents.
5.14 Refrains
from sharing workload or salary with other therapists except with
written agreement and only with fully
informed consent of client or employer.
The investigation was approved by an ethics committee (the Commission Nationale Informatique et Liberté) and
written informed consent was obtained
from respondents.
At least one member
from 71 families refused to participate, resulting in 315 family groups (381 adolescents) who gave
written informed consent (for more information see: Barnow et al., 2002a; Barnow et al., 2004a; Barnow et al., 2004b; Barnow et al., 2004c; Barnow et al., 2007).
Informed written consent was obtained
from parents of the children participating in the study, as approved by the ethics committee.
Written informed consent was obtained
from all participants aged 16 and above;
informed consent was provided by a parent or carer if the participant was below age 16.
Written informed consent was obtained
from all subjects.
Written informed consent was acquired
from all participating children and
from their parents.
From 2000 on, data were collected with
written informed consent in the winter of each year.
After obtaining
informed written consent from parents and adolescents and verbal assent
from children (aged below 12 years), a trained clinical psychologist or intern clinical psychologist administered the ADIS - IV - C / P.