
Dictate anywhere on your screen, capture telehealth audio straight from the call,
and skip the second login.
Shine Colcol
Fact checked by Dr. Ben Condon
This medical consent form template, also known as a patient consent form template, helps you clearly communicate the details of proposed treatment plans to patients before getting their consent to proceed.
With Heidi, you can generate medical consent forms that cover the following:
A medical consent form is used by medical professionals to acquire permission from patients or their legal guardians, before proceeding with a specific treatment or procedure. They are used by surgeons, anaesthesiologists, family physicians and many other specialists.
This form is crucial for ensuring patients are fully informed before undergoing any treatments or procedures proposed by their healthcare provider. The process of consent also involves the discussion of potential alternatives to the proposed treatment, including the option to forgo treatment altogether.
In the medical field, obtaining informed consent is an essential practice that ensures doctors are fulfilling their legal and ethical obligations. This standard has its roots in Reibl v. Hughes (1980, Supreme Court of Canada): consent is judged by what a reasonable patient would want to know, not what a reasonable doctor would think to disclose.
In this article, we’ll discuss the common types of medical consent forms, walk through how to create one for your practice, and share ready-made templates you can customise.
There are different variations of patient consent forms, each tailored to a specific need and doctor’s specialty:
This form is used for routine treatments, diagnostics, and non-invasive procedures. The patient signs only after their doctor has explained the purpose of the treatment, the risks involved, and any alternatives available to them.
Sometimes called a medical consent form for minors, this form allows parents or legal guardians to authorize medical treatment in place of children or minors. This is especially important when the patient is under the care of an adult guardian, as it allows them to receive necessary medical treatment even when their parents are not present.
One subtype worth noting is the grandparent medical consent form, which gives grandparents the authority to make healthcare decisions for a grandchild when the parents cannot be reached.
This form must be completed before any surgical procedure. It outlines the specific surgery, including laterality where relevant (e.g. left total knee replacement), associated risks, potential complications, and expected outcomes. The attending surgeon explains each element and the patient confirms their understanding.
In emergency situations where a patient cannot provide immediate consent (e.g., unconscious or incapacitated), doctors use this form to authorise urgent care.
This form is often pre-signed for minors, people with chronic conditions, or patients known to be at high risk of a medical emergency.
This form is used to confirm the patient’s agreement to take prescribed medications that affect mood, behaviour, or mental function, once they have been informed of the associated risks, potential side effects, and expected outcomes.
This type of consent form is especially important in the context of psychiatric care, where the patient’s autonomy is a crucial factor for treatment compliance.
In medical research, this form documents that participants understand the purpose, associated risks, and potential benefits of enrolling in a clinical trial. It’s also a requirement for any study involving human participants to meet legal and ethical standards.
Canada has no single national law on medical consent. Instead, each province legislates its own framework, covering what makes consent valid, how capacity is assessed, and what happens when a patient cannot consent on their own.
Here's how two provinces have built out that framework:
Ontario's Health Care Consent Act, 1996, covers three areas: treatment, admission to care facilities, and personal assistance services. Across all three, the Act establishes the following:
BC's Health Care (Consent) and Care Facility (Admission) Act governs consent for health care and for admission to a care facility, treating the two as related but separate processes. Here's how the Act frames each one:
Below is a quick guide to writing a medical consent form in your daily practice, along with an example to show how it works:
Open with the most important detail: the proposed treatment you're seeking consent for. Provide a short, precise description of the treatment or care plan and its purpose.
Example:
Proposed Treatment: The patient will undergo a colonoscopy to investigate the cause of persistent abdominal pain and irregular bowel movements.
Give a balanced overview of the treatment. This section should cover the expected benefits, risks, and where applicable, alternatives, including the option to forgo treatment altogether. This gives the patient enough information to make an informed choice.
Example:
Risks and Benefits: The benefits include an accurate diagnosis and the potential treatment of detected abnormalities. Risks include bleeding, perforation of the colon, and adverse reactions to conscious sedation.
Alternative Options: CT colonography was discussed as a non-invasive alternative, though the risk of missing small polyps was highlighted. The option to forgo the procedure altogether was also explained, along with the potential consequences of not undergoing screening.
This final section logs the patient’s response once all relevant information about the treatment is discussed. This includes the concerns raised, and the final decision for consent. It also covers the date and time consent was formally given, along with the attending physician's name and signature.
Example:
Patient Response: The patient expressed understanding of the procedure and voiced concern about the risk of perforation. They asked about the recovery time, and it was explained that most patients recover within a day, though mild discomfort may persist for a few days.
Consent Documentation: Consent was obtained verbally and entered in the patient’s electronic medical record (EMR).
Date and Time: 2023-10-15 at 10:30 EDT
Physician Signature: Dr. Emily Johnson, Family Physician
You can download a copy of this document, or auto-fill it seamlessly with Heidi, your AI care partner.
Patient consent forms are typically filled in by hand or typed up manually. It gets the job done, but it’s slow and prone to errors. Heidi gives you a faster, more accurate way to complete them.
A consent conversation deserves your full attention. When part of your focus is on getting the details down accurately, something in the room suffers. Heidi removes that tension.
Dr. Sanjay Mehta feels this on every visit. Heidi lets him keep his chair turned toward the family instead of the screen, so consent happens in conversation, not around a form. The hour he gets back from charting each day is more attention he can give the people in front of him.
Here's how Heidi keeps the conversation whole while the paperwork writes itself:
Heidi holds SOC 2 and ISO 27001:2022 certification, and complies with PIPEDA and applicable provincial health privacy legislation in Canada.
Built for Canadian clinical practice, this template helps you document every informed consent discussion in full, so it holds up to legal and ethical scrutiny. It covers treatment risks, benefits and alternatives, plus the process details that matter: verbal or written consent, date and time, and practitioner verification.
Informed consent is legally required across Canada before any examination, assessment, treatment, or procedure that carries potential risk. Written consent forms come into play more specifically for surgeries, invasive procedures, many psychotropic medication regimens, and participation in clinical trials or other health research.
LJ Acallar
Shine Colcol
LJ Acallar