Effects of two formats of informed consent on knowledge amongst persons with advanced HIV disease in a clinical trial of didanosine
| Autor: | S. Forde, Michael W. Ross, David Goldstein, David A. Cooper, Steven Barker, Brett Tindall |
|---|---|
| Rok vydání: | 1994 |
| Předmět: |
Adult
medicine.medical_specialty Research Subjects Human immunodeficiency virus (HIV) HIV Infections Medical practitioner medicine.disease_cause Medical care Consent Forms Patient Education as Topic Informed consent Health care medicine Humans Didanosine Informed Consent business.industry General Medicine Middle Aged Therapeutic Human Experimentation Clinical trial Family medicine Educational Measurement Comprehension business medicine.drug Hiv disease Clinical psychology |
| Zdroj: | Patient Education and Counseling. 24:261-266 |
| ISSN: | 0738-3991 |
| DOI: | 10.1016/0738-3991(94)90069-8 |
| Popis: | To determine subjects' perception of the purpose of informed consent, 113 subjects were recruited from a dosecontrolled clinical trial of didanosine (ddI). Subjects were surveyed regarding how they made decisions regarding their medical care in general, about how they obtained information about this trial in particular, and several aspects of the informed consent procedure. Subjects were then randomly allocated to receive information about the trial by either a written only format or a written and verbal format 1 week before commencement of the trial. An eight-item instrument assessed knowledge of ddI prior to and subsequent to receiving information. Most subjects obtained information about HIV-related issues from their specialist (70%) or general (51%) medical practitioner. A large proportion of subjects (88%) reported that they believed their specialist medical practitioner always acted in their best interest. The majority of subjects (79%) believed that subjects should be allowed the choice between participating in the clinical trial and receiving the drug outside the trial mechanism. Of the subjects, 96% believed that informed consent was necessary in clinical trials; however, their opinions of the purpose of informed consent varied widely. Although they signed the informed consent, 44% of the subjects stated that they did not understand ‘all’ of the information that was provided. We found that the provision of information by written mode alone, or written and verbal modes were both associated with significant increases in knowledge levels and that there was a significant interaction in the degree of change between the two methods, with the written plus verbal method showing the most improvement over time. There was an interaction between degree of improvement in knowledge of didanosine in subjects who received written information versus those who received written and verbal knowledge and time (pre- versus post-consent) and a significant main effect for time. All subjects were relatively well-informed about the drug and stated that specialist and general medical practitioners were their major source of knowledge for all aspects of their HIV health care. |
| Databáze: | OpenAIRE |
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