Research Study Enrollment
Recruit study participants with eligibility screening, consent forms, and health history
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What's Included in This Template
12 Fields
Pre-configured fields with the right input types, validation, and layout for application.
Full Customization
Change colors, fonts, add your logo, rearrange fields, and make it match your brand perfectly.
42+ Integrations
Connect with Mailchimp, HubSpot, Zapier, n8n, Google Sheets, Slack, and more. Automate your workflow.
Form Structure
Multi-page layout keeps your form organized and easy to complete.
The last required question on this template reads "I consent to participate in this study," and it offers two answers: "Yes, I consent" or "I have questions first." That second option is the point. A recruitment form that only accepts a yes pushes people to agree before they're ready, which is exactly what an ethics board doesn't want to see. This one leaves room for hesitation and captures it as data.
Screening, health history, and consent in one sitting
The Research Study Enrollment template runs 12 fields across four pages, which keeps a 12 to 18 minute task from feeling like one endless scroll. It opens with identity and contact basics: full name, email, phone, and date of birth, plus a gender question with Non-Binary and Prefer not to say among the options. Then it moves into clinical territory. A required Medical History Summary sits beside an optional Current Medications box, and a yes or no question asks whether the person has participated in a research study before. Emergency contact name and phone are both required, so you're never chasing those details after someone is already enrolled. The form closes with the consent question and an open box for questions or concerns, giving hesitant prospects somewhere to speak up instead of quietly closing the tab.
Who runs their recruitment through this form
Anyone enrolling human participants: psychology labs screening undergraduates, coordinators filling clinical trial cohorts, public health teams building longitudinal panels, graduate students who need a defensible consent record for a thesis study. The structure does a first eligibility pass for you. Date of birth confirms age requirements, the prior participation question flags experienced subjects, and the medication and history fields surface exclusion criteria before you spend time on a screening call. Because responses carry health information and consent records, the template lives on Uplup's Business plan.
Rewriting it for your protocol
Every field is editable, so the consent statement can match your IRB-approved language word for word, down to the study identifier. Add fields for protocol-specific criteria, drop the ones you don't need, and mark anything sensitive as optional. Traditional mode is the recommended setting here, one page of related fields at a time with a progress bar and back navigation, which suits a form people fill in carefully. When it's ready, share it by link or QR code at recruitment events, embed it on your lab's site, or place it in a WordPress page with the Uplup plugin's shortcode. Responses collect in a dashboard with per-question breakdowns, export to CSV for your screening log, or flow out through webhooks and Zapier to wherever your team tracks candidates.
Who Is This Template For?
This template works for a wide range of goals and industries.
Clinical trial cohort recruitment
Coordinators collect eligibility basics, a required Medical History Summary, current medications, and a consent decision in one pass, so prospects arrive at the screening call already pre-qualified.
University lab studies
Psychology and behavioral labs screen student participants with date of birth, prior study participation, and emergency contact details, keeping a clean enrollment record for every subject.
Public health and longitudinal research
Teams building panels over months or years capture contact details, health history, and documented consent up front, then export the roster to CSV as the study population grows.
Key Features
Consent question with a built-in pause
The required consent field offers "Yes, I consent" or "I have questions first," so undecided prospects stay in your pipeline instead of abandoning the form.
Eligibility screening across four pages
12 fields move from contact details through medical history and prior study participation, surfacing exclusion criteria before anyone books a screening call.
Emergency contact capture
Required emergency contact name and phone fields mean every enrolled participant has a reachable contact on file from day one.
How It Works
Choose This Template
Click "Use This Template Free" to get started. You will get a full copy of this form in your account, ready to edit.
Customize It
Edit the fields, update the design, add your branding, and set up integrations. Everything is editable from the visual builder.
Share & Collect Responses
Publish your form and share it with a link, embed it on your website, or post it on social media. View responses in real time.
Frequently Asked Questions
Do participants have to give consent to submit the form?
Can I edit the consent wording to match my IRB-approved language?
How do I get enrollment data to the rest of the study team?
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