Human Research Consent Form

Human Research Consent FormEverybody should be able to make informed choices about their medical care. Treatments for medical conditions can be sensitive, so patients must be able to decide according to the known risks as well as their own personal preferences, how they will be treated. Therefore, before medical workers are allowed to be able to treat their patients, they have to obtain the process of informed consent.

Informed consent constitutes a lawful condition under which a patient has been given a complete and accurate description of his or her physical state and the treatment suggested by the treating physician. After receiving this information the patient is required to give the doctor their consent to treat before any form of care is delivered. Without informed consent from the patient an health care professional cannot provide treatment.

Decision Making Capacity

In certain instances patients lack the ability to comprehend their options in terms of treatment and the risks/benefits of each one. In some instances patients might not be able convey their preferences to health professionals. In these situations the patient is said to lack the necessary capacity for decision-making. Family members or a court-appointed representative will then be permitted to take over informed consent.

Patients who are greatly influenced by their emotions such as anxiety or fear for instance they could be judged as not having the capacity to make decisions. Those who are unconscious clearly are unable to make decisions on their alone, and external parties require consent for treatment instead.

Items in an Human Research Consent Form

There are certain elements that are commonly included in informed consent forms:

The patient’s medical condition or diagnosis

The treatment that is recommended by the medical professional in charge

The risks and benefits associated with this method of treatment

Alternative treatments are readily available, as well as their benefits and risks

The benefits and risks associated with not accepting any treatment at all

These items must not only be documented however, they must discuss the situation with patients. In this way, he or can fully comprehend the specifics of the situation and get straight answers to any questions that may have arisen.

Download Human Research Consent Form

Human Research Consent Form

Human Research Consent Form

Human Research Consent Form

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