Blog | Little Journey

The ‘last mile’ of recruitment: Supporting patients before they say yes

Written by Little Journey Limited | Apr 28, 2026 12:52:03 PM

Clinical trial support tends to be treated as two separate phases:

    • Recruitment: strategies and vendors focus on sourcing the right potential participants (awareness campaigns, social media targeting, referrals, pre-screening, etc.)
    • Retention: strategies and vendors focus on enrolled patients (communications, reminders, ePRO, patient engagement, etc.)

But between those two phases is an under-supported window that can erode recruitment efficiency before typical retention strategies have even been introduced.
This is the ‘last mile’ of recruitment, or enrolment phase: the decision-making window where someone has been made aware of a trial they may be eligible for but hasn’t yet committed to participating.

And it’s not a minor phase. It’s where patients and their families decide whether participation feels clear, feasible, and worth it in the context of real life. It’s also where sites end up doing the heavy lifting of expectation-setting and reassurance, often with limited time.

In recent months, our research team has focused on this ‘last mile’: what makes eligible, interested patients and families hesitate, and where support currently falls short.

To keep this grounded in real clinical workflows, we spoke with Chloe Lane, a Paediatric Research Nurse, as an external subject matter expert, alongside people who have first-hand experience of considering participation in clinical trials.

Why the enrolment phase is crucial for successful clinical trials 

“Enrolling onto a clinical trial can be a huge commitment and there are lots of factors to consider; particularly when it comes to children and their families. When we provide holistic support in the enrolment stage, we can begin to build trusting relationships, which can directly improve patient retention and trial success.”
- Chloe Lane, Paediatric Research Nurse

What ‘last mile’ support usually looks like today (and where it’s lacking) 

In a typical trial, the enrolment phase is supported through some combination of:

    • Participant information sheets and consent documents
    • Site-led phone calls and appointments
    • Sponsor- or CRO-provided PDFs and packs (variable in quality, timing, and relevance)
    • Informal guidance from staff based on experience

These elements are essential but they’re not always sufficient, and they’re rarely designed as a coherent patient experience. They can feel like ‘information’ rather than ‘support’ that helps families with practical decision making.

Information overload is a common challenge, with research staff often having to break documents down themselves to make information more digestible for families. 

 “I'll break it down quite simply and then put it into a table format or list to the families what's expected of them when they come in. This might be blood test first thing, followed by this, this and this… They're always super, super grateful for that”
- Chloe Lane, Paediatric Research Nurse
 

The 6 main friction points during the enrolment phase

Across the insights we gathered, the friction points tend to cluster into six areas.

1) Screening in an unknown “black box”

Many people assume being approached about a trial means they will be enrolled. The steps between interest, screening, and consent aren’t widely understood.

When different screening outcomes aren’t clearly explained upfront, patients and their caregivers can feel disoriented, even if the process is appropriate and ethical. Sponsors and sites then carry the downstream cost: disappointment, drop-off, and reduced trust within patient communities.

What this tells us: “What happens next” needs to be made clear right from the start to set expectations without creating fear.
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"We were really keen to get on the trial […] having multiple steps (things to do) during this time can add to the worry about whether you’ll be accepted onto the trial.”
– Caregiver feedback on trial experience

 

2) Information overload does not support informed decision-making

The enrolment phase often begins with long documents and new, complex concepts. Even highly engaged potential participants can struggle to interpret what matters now versus what can wait.

Patients and their families need an accessible starting point: What is this trial? Why me? What does participation look like? What are the real trade-offs?

What this tells us: Early enrolment support should reduce cognitive load: start with clarity, then layer detail.

 

3) Potential participants need the trial translated into “real life”

Even when someone is interested, their decision can hinge on feasibility:

    • travel time and cost
    • time off work or school
    • visit duration and unpredictability
    • what to bring, who can attend, whether siblings can come
    • what happens if symptoms flare or plans change

These are the details that determine whether participation is realistic - and they’re not always communicated early enough, consistently enough, or in a way people can act on.

What this tells us: The last mile is as much a logistics problem as it is an information problem.

 

4) Questions go unanswered

Patients, and their wider family and support network, often have concerns they don’t voice. They may feel unsure what’s appropriate to ask, worry about appearing difficult, or simply not know what questions matter until later.

Often that means the people who most need reassurance can be the least likely to request it.

What this tells us: Good pre-enrolment support should actively prompt and normalise questions, not passively wait for them.



5) The “unhappy path” matters

The last mile isn’t only about getting to “yes.” It also includes what happens when a patient becomes ineligible, fails screening, or decides not to proceed.

A respectful offboarding experience protects trust, strengthens your reputation with patient communities, and supports future willingness to engage with research.

What this tells us: Good pre-enrolment support should be designed for the unhappy path as standard. It is a crucial part of ethical, patient-centric recruitment.


6) Sites are already trying to bridge the ‘last mile’ gap

In reality, research teams are often:

    • interpreting dense documents
    • setting expectations for screening, timelines, and visit flow
    • translating the protocol into plain language
    • collecting background details early so the first touchpoint is productive
    • managing disappointment and offboarding compassionately

This work is valuable, but time consuming. It also varies depending on staff capacity and experience, creating inconsistency in participant experience across sites.

What this tells us: Sponsors have an opportunity to standardise high-value support that adds to the human relationship sites provide.

 

Why this is a strategic gap for sponsors 

The clinical research industry hasn’t consistently operationalised the ‘last mile’ as a defined phase with its own needs, success criteria, and support components.

If sponsors can treat the enrolment phase as a deliberate part of recruitment, then pre-enrolment support can become a driver for:

    • clearer, more confident screening and enrolment decisions
    • fewer drop-offs due to avoidable confusion
    • reduced site time spent repeatedly translating patient information into something patients can actually understand
    • stronger trust and experience across both “yes” and “no” enrolment outcomes

What good ‘last mile’ support must achieve

Based on our research insights, effective last mile support should:

    • Make next steps predictable (screening and consent explained clearly)
    • Reduce cognitive load (clarity first, details layered after)
    • Translate trial participation into real life (support logistics and set expectations)
    • Prompt and support questions (especially unspoken ones)
    • Respect the unhappy path (use human > scientific language, with sensitive signposting)
    • Fit site workflows (supporting research teams, not adding burden)

These needs map directly to the six friction points we saw most often.

The ‘last mile’ of recruitment is where decisions are still being made, and small improvements to the level of support can have outsized impact for patient experience and trial outcomes.

How Trial Flow fits in

“As a paediatric nurse working in clinical research, I felt as though the team at Little Journey truly valued my insight, experience and feedback in these early stages of product development. This commitment to collaboration gives me confidence that they will positively contribute to the experiences and outcomes for children and their families and it is exciting to know that such products are in development.”
- Chloe Lane, Paediatric Research Nurse

If your team is working to improve recruitment rates, patient experience, and trial efficiencies - without increasing site burden - we’d love to chat about how Trial Flow can help.