Sentences with phrase «provided written informed consent»
The study received institutional review board approval from The Johns Hopkins University, and all participants provided written informed consent; parental consent was not required because these adolescents were seeking confidential health services.
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All study participants gave written informed consent, and one of parents provided written informed consent on behalf of the children involved in the study.
Following the initial screen using the STSC, children meeting entry criteria were invited to take part in the full study and mothers provided written informed consent.
Mothers who provided written informed consent were mailed questionnaires prior to the interview to return at the time of the clinical assessment.
All participants and the parents of those aged below 16 provided written informed consent to participate in the study, which was approved by the University Ethics Committee and the Southampton City Council and Hampshire County Council's Children's Services Research Governance Committees.
All patients provided written informed consent and this study was approved by each sites institutional review board for research with human subjects.
After Institutional Review Board approval, parents provided written informed consent, and adolescents gave written assent.
Participants provided written informed consent for participation at each research assessment.
Before commencing study, all parents provided written informed consent while children provided written assent.
Primary caregivers provided written informed consent to take part in the research and also provide written informed consent on behalf of their participating child / children.
After a complete description of the study to the subjects, all participants provided written informed consent.
All participants provided written informed consent and were compensated for their participation.
All participants provided written informed consent prior to the study.
All parents or guardians provided written informed consent to participate in the study and were free to withdraw from the research at any time.
Principals (or an authorised representative) provided written informed consent for their school to participate, or declined participation, using a unique web - link for each school.
For those interested in participation, each member of the couple subsequently provided written informed consent and was assessed for the inclusion / exclusion criteria.
Each mother provided written informed consent before participation.
Parents and children aged 16 years and older provided written informed consent and children under 16 provided assent.
Each participant provided written informed consent, and completed a questionnaire stating reasons for attendance, age, symptoms of urethritis, number of lifetime sexual partners, history of STIs and recent / current antibiotic treatment.
The study was approved by the relevant institutional review boards, and all patients provided written informed consent.
Eligible participants were then invited to an interview and questionnaire assessment, at which time they provided written informed consent to participate.
These data collection procedures (as well as the procedures described in study 2 and 3) were approved by the Human Subjects Review Board on the campus in which this research was conducted; parents provided written informed consent.
Quiz Ref IDOne parent or parent surrogate (subsequently referred to as «parents») of each adolescent provided written informed consent, and the adolescents provided written informed assent before adolescent interviews.
All participants provided written informed consent to participate.
One parent or parent surrogate (subsequently referred to as «parents») of each adolescent provided written informed consent, and the adolescents provided written informed assent before adolescent interviews.
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.
A parent - proxy provided written informed consent.
Parents provided written informed consent before participating in the focus group.
The project was approved by the Regional ethical review board in Umea, Sweden (Dnr 05 - 044M) and volunteers provided written informed consent.
All participants provided written informed consent prior to survey participation.
Ethics approval The ethics committee of Wuhan Union Hospital approved the study, and all participants provided written informed consent prior to enrolment.
All participants provided written informed consent after study procedures were explained.
All participants provided written informed consent.
All subjects provided written informed consent approved by the Institutional Review Board.
The study protocol was approved by the University of Auckland Human Ethics Committee (reference 2006/462), and all participants provided written informed consent.
A direct parent (mother or father) provided written informed consent.
All patients provided written informed consent for the studies performed.
Patients 18 years and older provided written informed consent.
All provided written informed consent before assisting with the study.
Institutional review board approval was obtained at each clinical center and all participants provided written informed consent.
The subjects provided written informed consent to participate in the study.
The Netherlands Organization for Health Research and Development (ZonMw) approved the study protocol and all participants provided written informed consent.
All participants provided written informed consent.
Nineteen healthy subjects without a psychiatric history (age mean / SD: 29/7.8; gender: 14 male, 5 female)(Table 1) participated in this study after providing written informed consent as approved by the medical ethics committee for research in humans (METC) of the University Medical Center Utrecht, The Netherlands.
Participants read an information sheet initially outlining the nature of the research before providing written informed consent.
They all had the ability to understand and provide written informed consent in English, had access to a telephone during the program period and were identified as having mild / moderate depression when screened using the Patient Health Questionnaire (PHQ9).
All participants are required to provide written informed consent.
After providing their written informed consent, both partners independently completed an online battery of questionnaires.
Not exact matches
After written informed consent, these participants provided a single, 10 mL aliquot of freshly expressed milk (mature milk).
An editorial in the The New England Journal of Medicine recommends that patients provide informed, written consent to undergo elective surgery by physicians who haven't had enough sleep.