Sentence examples for conduct the consent from inspiring English sources

We are evaluating using the internet and mobile devices to conduct the consent process and study visits in a streamlined pediatric asthma trial.

If mothers are targeted as the primary consenters for children's studies, participation in consent may be increased by having female research workers conduct the consent discussion; it would be valuable to conduct further research to test this hypothesis.

We have uncovered a need for greater understanding of how to conduct the consent process when researchers face the double challenge of including vulnerable adults in cluster-randomised trials.

To allow clients to be recruited at times when the research assistants were not present and thereby increase the diversity of the client sample, the participating cosmetologists were also trained to recruit the salons' clients to the study and conduct the consenting process on their own.

Staff at the clinic sites initiated recruitment communications with the subjects, conducted the consent process, and scheduled the telephone interview.

Consent will be documented by patient's dated signature on a consent form along with the dated signatures of the person conducting the consent discussion.

Physicians qualified to conduct the informed consent process must be certified in the protection of human subjects for research.

Mijikenda research staff (field workers), fluent in local and national languages and with secondary school education, visit families to conduct the informed consent process and collect information and blood samples according to the study protocol.

Permission to conduct the study and consent to participate in the study will be sought from relevant authorities and participants, respectively.

The informed consent was countersigned by the personnel who had conducted the informed consent discussion who was qualified according to local regulations.

Investigators described the protocol to potential volunteers face to face, and informed consent was obtained by the use of a written IRB-approved consent form, signed and dated by the volunteer and the investigator who conducted the informed consent discussion.