Parental Consent Clinical Trial
Official title:
Effectiveness of the Consent Process Used for Outpatient Endoscopy
The purpose of this study is to evaluate the effectiveness of the consent process currently used for outpatient endoscopy procedures at our hospital. Results from this study will be used to assist in making improvements in the way we communicate with parents, thereby enhancing the ability to provide informed consents.
Obtaining informed consent before performing an invasive medical procedure or treatment is a
crucial component of patient care. The manner in which the consent process is conducted
impacts the doctor/patient relationship, patient safety and patient satisfaction. Many
times, patients sign consent forms without reading or understanding them. Although the form
has been signed, true informed consent has not been obtained. While there are many variables
that impact the ability to truly consent, ineffective communication between the patient and
health care providers hampers the process.
Evidence shows that improving the consent process by ensuring effective communication
between the child's parent and health care team affords substantial benefit. A consent
process well done strengthens the parent-provider relationship. It positively impacts risk
management. It improves patient safety. It diffuses would-be litigants by helping parents
have realistic expectations of care. The consent process should allow and encourage parents
to exercise both their right and their responsibility to take an active role in their
child's health care.
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Observational Model: Ecologic or Community, Time Perspective: Prospective
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT02570061 -
Recruiting to Clinical Trials on the Telephone
|
Phase 3 |