A health-tech habit is not a marketing permission
CIHI's current indicator reports that 51.5% of adults said they use technology to understand and manage their health. The 2025 result is useful context for how Canadians engage with health technology. It does not show that a visitor expects a clinic to use a page visit, a service question or a form response for advertising, profiling or any purpose beyond the one explained to them. CIHI's indicator
The distinction matters before a form is submitted. Someone can be comfortable looking up a health question online and still want a clinic to explain what happens to the information they provide. A tidy booking flow should not make a person guess whether a request will reach a clinic team, an analytics platform, an advertising platform or another service provider.
What the Canadian indicator measures — and what it does not
Statistics Canada released the underlying 2025 Canadian Community Health Survey results on 3 September 2026. Data was collected from 2 January to 31 December 2025 and weighted to represent adults age 18 and older living in the provinces. The annual release does not include territorial estimates because the 2025 survey does not represent the entire territorial population. Statistics Canada's release
The 51.5% measure is narrow: respondents had to agree or strongly agree with five statements about finding health information with technology, understanding health problems, deciding what care is best, sharing health information and organizing health information. It is a population indicator, not a test of a clinic website, a booking tool, an accessibility review, a privacy program or an individual's consent choice.
- Geography and population: adults age 18 and older living in the provinces; the 2025 annual release excludes territorial estimates.
- Method: weighted self-reported survey responses. The numerator requires agreement with all five technology-use statements; non-response categories and proxy responses are excluded.
- Coverage limits: the CCHS excludes people living on reserves and in other Indigenous settlements in the provinces, full-time Canadian Armed Forces members, institutionalized people, and residents of two Quebec health regions. CIHI says these exclusions total less than 3% of the adult population.
- Interpretive limit: the result cannot say whether a person wants online booking, can complete a particular form, accepts tracking or has agreed to a clinic's use of data.
A clear purpose is part of a clear inquiry
Canada's federal privacy commissioner says meaningful consent requires people to understand the nature, purpose and consequences of a collection, use or disclosure of personal information. The office also says the form of consent should reflect sensitivity and the circumstances. That is general guidance, not a substitute for advice on a clinic's provincial, professional or vendor-specific obligations. Office of the Privacy Commissioner of Canada guidance
For a public clinic page, the practical question is smaller than a full privacy program: can a person see what the form is for before they are asked to share anything? If the request is for a callback, say so. If a referral is required, say so before the form. If a question needs clinical judgment, route it to the appropriate team instead of using a marketing form to collect symptoms or treatment history.
AKIERO's operational read: separate routing from measurement
This is AKIERO's operational interpretation, not a finding from the survey. A clinic can measure whether a page helps suitable people reach the right team without making its form a catch-all record. The minimum useful information for an inquiry should be set by the real handoff: the service, location, contact route and team owner.
Then trace what happens around that handoff. Review the questions in the form, the confirmation page, the inbox or booking system, and the analytics or advertising tags that fire along the way. The goal is not to turn every visitor into a tracked audience. It is to make the path understandable, avoid collecting details the route does not need and give the clinic a chance to check its own rules before a change goes live.
This differs from whether a clinic's clinical systems exchange information effectively. As explained in a digital clinic is not automatically easy to book, clinical information exchange and a prospective patient's first public step solve different jobs. Both deserve a named owner.
- Use the service and location to route an inquiry before asking for free-text detail.
- Offer the contact option the clinic can actually staff, including a phone route when appropriate.
- Keep clinical notes, symptoms, diagnoses and treatment histories out of general marketing and analytics tools unless the clinic has a reviewed, appropriate process for them.
- Make one person responsible for checking the form, confirmation and destination after changes to a tag, vendor or booking flow.
Start with one visible promise
Choose one high-intent service page and ask a colleague to use it on a phone without entering real personal or health information. Can they identify the service, location, referral requirement and next step? Can they tell why the form asks for each field? Can the clinic explain who receives the request and how it is handled? Those are useful operating questions before adding another campaign or another form field.
Use the clinic booking-path check to review that single route. If the page and handoff are sound but the team cannot see whether suitable inquiries become appointments, AKIERO's patient-conversion service can help connect the public path to booked and attended appointments without treating marketing systems as clinical records.
Sources and scope
This article offers general marketing and operational information, not legal, privacy, regulatory or clinical advice. Rules vary by province, profession, channel and use case.
- Canadian Institute for Health Information, Canadians Who Use Technology to Understand and Manage Their Health, accessed 17 October 2026. The current indicator result, calculation, coverage and caveats.
- Statistics Canada, Data availability: Shared Health Priorities Indicators for Adults, 2025, released 3 September 2026. 2025 collection period, provincial coverage and weighted adult population.
- Office of the Privacy Commissioner of Canada, PIPEDA Fair Information Principle 3 — Consent, accessed 17 October 2026. General consent guidance; requirements vary by province, profession and use case.

Donna Philipe
AKIERO ResearcherAn AKIERO editorial persona focused on primary-source research, policy and healthcare demand.
