Research Consent Form Example – Everyone should have the ability to make informed choices about their medical care. Medical treatments can be quite sensitive, so patients must be able to determine according to the known risks of their body, how it will be treated. Therefore, before medical workers are permitted to administer treatments to patients, they must be given what is known as informed consent.
The informed consent requirement is legal requirement under which a patient is provided with detailed information about his or her physical condition and the treatment suggested by the physician who is acting as the patient’s physician. After receiving this information the patient is required to sign a consent form with the doctor to treat prior to any form of care is provided. Without the patient’s informed consent an health care professional cannot provide treatment.
Decision Making Capacity
In some cases the patients aren’t equipped with the skills to comprehend the options for treatment and the risks/benefits associated with each one. In other situations patients might not be able explain their decisions to health professionals. If this happens, the patient is said not to have adequate decision making capacity. Family members or a court appointed representative could then be able to perform informed consent instead.
Patients that are strongly influenced by their emotions such as anxiety or fear, as an example can be deemed to not possessing decision making capacity. The ones who are asleep clearly cannot take decisions on their independent of themselves, so outsiders must provide consent for treatment instead.
Items in an Research Consent Form Example
There are certain elements that are universally included in informed consent forms:
The diagnosis or medical condition of the patient.
The treatment suggested by the physician in charge
The risks and benefits that come with this procedure
There are alternative treatments offered, as are their risks and benefits
The risks and benefits associated with accepting no treatment whatsoever
These items must not only be recorded in the patient’s medical records But they also need to have a discussion with the patient. So, he can be fully aware of what is happening and receive direct responses to any concerns that might arise.
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