[Case 04]

Structured UX Research Plan for Healthcare Services

Healthcare

Improving Healthcare Experiences through UX Research

Building a Research Framework for Patient-Centered Solutions

[Project Overview]

Healthcare services often struggle with unclear communication and long wait times. We created a structured UX research plan—covering stakeholder mapping, recruitment, interview/survey design, and ethics—to reveal gaps and guide patient-centered improvements.

[Problem Statement]

Without a systematic research approach in the clinic, insights risk being fragmented or biased and can’t reliably inform future service design.

[Industry]

Healthcare

[My Role]

UX Researcher

[Platforms]

Healthcare Service Context

[Timeline]

January 2025 – March 2025

[Process]

[01] Research Planning

Built recruitment plan, consent materials, and communications calendar.

Established data-security and privacy procedures (TCPS 2 aligned).

Analyzed academic literature and competitor systems to benchmark best practices for engagement.

[02] Discovery (Interviews & Surveys)

Conducted interviews/surveys with patients, caregivers, front-desk staff, and doctors/nurses.

Collected pain points on scheduling, wait times, and information clarity.

Synthesized themes to inform low-fidelity concepts.

[03] Low-Fidelity Prototyping

Sketched concepts like voice-guided appointment and consultation reminders.

Outlined process flow and key screens for testing tasks.

Prepared materials for inclusive testing (language/hearing support).

[04] Usability Testing & Refinement

Tested with diverse users; captured task completion and clarity feedback.

Iterated wording, flows, and reminder timing based on findings.

Compiled final report with journey maps, prototype updates, and next-step recommendations.

[Outcome]

A clear, ethical research framework.
A stakeholder-aligned roadmap for discovery and testing.
Actionable outputs—journey maps, low-fi concepts, and consent materials.

[Key Learnings]

Ethics is foundational

Consent, privacy, and voluntary participation build trust and improve data quality.

Multi-stakeholder input reveals system gaps

Patients, caregivers, staff, and clinicians surface different pain points.

Lightweight prototypes accelerate alignment

Simple concepts (voice guidance, reminders) make research findings tangible.

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