01 — Overall Strategy

Clinical Recruitment
Ecosystem

Clinical trial recruitment has long been treated as a one-way, transactional search, often overlooking the complex psychological landscape of patients caught between seeking new treatment and maintaining the status quo.

Focusing on Treatment-resistant Hypertension, this project applies service design thinking to pivot the traditional recruitment model toward a "Connected Community" experience. By prioritizing the patient’s "Right to Know" and "Psychological Safety," we dismantled information barriers and built trust-based connections, significantly increasing the willingness of target populations to engage in clinical research.

02 — What did I do?

Role

UX Research + Strategy, Interaction Design,Wireframing, Low-fi and Hi-fi Mockups,
Graphic Design.

Who'd I work with?

In collaboration with the doctor in clinic, Product Team and 12+ local retail stakeholders.

03 — The Challenge

The problem with promoting new medical use devices...


For the company, a certain number of patients is needed.

For physicians, within a limited time, it is difficult for them to introduce clearly, which leads to mistrust.

For patients: this disease is not a life-threatening one; they are not in a hurry to make decisions, but medical companies already meet the deadline to scale it up to clinical use.

For all-in-one clinical recruitment websites: mainly designed for serious diseases, used as a search tool for patients when they had no other choices but to grab at straws.

The ideation

How might we alleviate the worry and inform them of the risks of the new treatment for our target patients?

03 — Research & Insights

Bar chart showing willingness to participate by channel

The Trust Threshold

Quantitative data revealed that 68.9% of patients are most likely to trust information received in-person at a specialist's office. Conversely, digital website advertisements scored nearly 30% lower in trust.

Strategy: The Digital Portal must mimic the specialist's authority to bridge this trust gap.

Mapping Psychological Friction

Observations across the patient journey identified critical "Pain Points":

  • 01.

    Before: High anxiety regarding professional medical knowledge.

  • 02.

    During: Distrust stemming from complicated document signing.

  • 03.

    After: A total lack of systematic follow-up guidance.

Diagram of research observations across Before, During, and After stages

04 — Design Rationale

De-layering Medical Complexity

"I optimized the patient-facing enrollment workflow not by making it shorter, but by making it smarter. By introducing 'Qualified Friction' during eligibility checks, I reduced user anxiety through clear risk communication and improved the clinical approval cycle by delivering higher-quality candidate data."

Qualified Friction in Onboarding

While traditional UX aims for zero friction, clinical recruitment requires "Qualified Friction". I designed the eligibility flow ("Is This Trial Right for You?") to act as a supportive filter. This ensures candidates feel informed about risks while providing high-quality data to the Medical Device Company.

05 — System Architecture

Aligning Multidisciplinary Stakeholders

My Stakeholder Map and Service Blueprint revealed that success depends on more than just a website. It requires a synchronized "Line of Visibility"between:

The Frontstage (Patient/Doctor)

"A Patient-Centric Portal that bridges the gap between complex medical knowledge and clinical decision-making. By integrating eligibility screening and phased surgical navigation, the interface transforms medical data into an empathetic journey to reduce pre-procedural anxiety."

The Backstage (Company/FDA)

"The backend synchronizes data between hospitals, data centers, and regulators. It automates candidate filtering and manages real-time feedback loops, allowing the medical company to optimize product iterations based on post-operative statistics and clinical support training."

06 — End-to-End Care

Addressing the "After Surgery Concern"

Most recruitment tools end at signup. I extended the UX to include Post-Procedure Follow-Up and Coordinator Led Care. By addressing long-term effects and potential side effects in the UI, we build a "Connected Community" that encourages participants to share and give feedback.

Diagram of research observations across Before, During, and After stages

Stakeholder Map

07 — demo