Consent Form For Quantitative Research – Every person should be able to make informed choices about their health. Medical treatments can be quite demanding, and therefore patients should be able, in the end, to decide according to the known risks as well as their own personal preferences, how they will be treated. In order to ensure that medical professionals are allowed to treat patients, they must obtain the process of informed consent.
A patient’s informed consent can be a legally binding requirement where a patient is provided with a full and complete description of his or her physical health and the treatment recommended by the acting physician. After receiving this information patients must give the doctor their consent to treat prior to any form of treatment is delivered. Without informed consent from the patient any health professional is not allowed to provide treatment.
Decision Making Capacity
In some instances patients may not have the capacity to comprehend their options regarding treatment, and the risks/benefits associated with each one. In some instances, patients may not be able to effectively communicate their decisions to the health workers. In these situations it is believed that the patient not to possess the proper capacity to make decisions. The family member, or court-appointed representative could then be able to take over informed consent.
Patients who are greatly influenced by their emotions – such as anxiety or fear, for example can be deemed to not possessing decision making capacity. The ones who are asleep clearly cannot make decisions on their own, and outside parties need to consent to treatment instead.
Items in an Consent Form For Quantitative Research
Certain elements are generally included in informed consent forms:
The patient’s medical condition or diagnosis
The recommended treatment is suggested by the acting physician
The risks and advantages associated with this procedure
Alternative treatments are available, as well as their risks and benefits
The risks and benefits associated of refusing treatment at all
Not only should these details be detailed in documentation However, they should also discuss the situation with patients. This way, he or can be fully aware of the specifics of the situation and can get direct answers to any questions that have arisen.
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