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Understanding of Consent in Clinical Research
Clinical trial pipeline · Data from ClinicalTrials.gov
See which Understanding of Consent in Clinical Research trials you may qualify forClinical trial pipeline · Data from ClinicalTrials.gov
See which Understanding of Consent in Clinical Research trials you may qualify forThis pilot randomized controlled trial evaluates the impact of video-enhanced consent compared to the usual approach. The investigators aim to assess if video-e…
The psychosomatic symptoms of patients with differentiated thyroid cancer (DTC) during the initial treatment phase need to be improved. Stress coping training a…
The primary purpose of this pilot quality improvement study is to assess the impact of a brief introductory discussion about Learning Health Care (LHC) and clin…
There is evidence that the current design and content provided by most biomedical research informed consent documents do not consistently meet the expectations…
The Informed Consent (IC) of a medical procedure is the aceptation of a diagnostic or therapeutic procedure by the patient, after receiving the necessary and ac…
This study is a randomized trial in which participants are assigned to one of 2 strategies of information notice administration which include the standard appro…
Background: Sickle cell disease is an inherited blood disorder. People with this disease have a problem with their hemoglobin. That is a protein in red blood c…