Built for Academic Scientists

Clinical Research SoftwareWithout the Enterprise Overhead

No IT department. No procurement delays. No $100k budgets. Launch your IRB-approved study today with ePRO, eConsent, and real-time analytics.

See How It Works
No credit card requiredIRB documentation includedLaunch in under 1 hour

Who Uses Capture.Study?

From dissertation research to multi-center trials, we serve the full spectrum of academic research.

PhD Students

Running dissertation studies with limited budgets

Postdocs

Managing multi-site collaborations across institutions

Research Coordinators

At academic medical centers needing efficient tools

Principal Investigators

Managing grant-funded studies with compliance needs

IRB Administrators

Evaluating platforms for institutional approval

Academic Research Shouldn't Be This Hard

We built Capture.Study because we know the pain of enterprise EDC systems.

REDCap requires IT support

Self-service, no technical setup

Procurement takes months

No purchase orders, start today

Paper consent is error-prone

eConsent with digital signatures

Participants don't complete surveys

Mobile-first, QR enrollment

Data entry is manual

Real-time direct capture

Multi-site is complex

Built-in site management

Study Types We Support

Purpose-built for the full range of academic research designs.

Observational Cohort Studies
Cross-Sectional Surveys
Longitudinal Patient Registries
Behavioral Intervention Trials
Pilot Feasibility Studies
Survey Validation Studies
Multi-Site Collaborative Research
Quality Improvement Projects
Thesis & Dissertation Research

Everything You Need for Academic Research

ePRO, EDC, eConsent, and multi-site management in one platform.

ePRO / eCOA

Electronic Patient-Reported Outcomes

Collect high-quality patient data directly from participants on any device. Mobile-first design means higher completion rates and better data.

  • QR code enrollment (no app install required)
  • 10+ question types (VAS, Likert, NRS, etc.)
  • Skip logic and conditional branching
  • Questionnaire versioning with audit trail
  • Pre-built diary templates (sleep, pain, mood)
  • Real-time data validation
Browse ePRO Templates
Mobile-First Experience

Visual Analog Scale (0-100)

Numeric Rating Scale

0
1
2
3
4
5
6
7
8
9
10

Likert Scale

Strongly
Disagree
Neutral
Agree
Strongly
Digital Consent Workflow
1
Participant reviews consent sections
2
Comprehension check questions
3
Digital signature capture
SHA-256 hash + full audit log
eConsent

IRB-Compliant Electronic Consent

Replace paper consent with a secure, auditable digital workflow. Participants sign on their own device, and you get a complete compliance record.

  • Section-based consent builder
  • Digital signature capture (legally binding)
  • Consent versioning for protocol amendments
  • Full audit trail (IP, timestamp, user agent)
  • PDF export for IRB records
  • Cryptographic signature verification (SHA-256)
View Consent Templates
Multi-Site

Academic Collaboration Made Simple

Run multi-site studies across institutions without the complexity. Each site gets their own enrollment, while you maintain central oversight.

  • Site-specific QR codes for enrollment
  • Participant numbering by site (e.g., 001-0042)
  • PII segregation (coordinators see names, PIs see codes)
  • By-site enrollment tracking and dashboards
  • Cross-institutional data access controls
  • Site coordinator role with limited permissions
Site Overview Dashboard
Johns Hopkins45/50
Stanford38/50
UCLA52/50
Publication-Ready Exports
study_data.csv
Wide Format
codebook.csv
Data Dictionary
audit_log.csv
Compliance
study_data.xpt
CDISC/SAS

Compatible with SPSS, R, SAS, Stata, Python, and Excel

Data Exports

Publication-Ready in One Click

Export your data in formats ready for statistical analysis. No data wrangling required—just download and analyze.

  • CSV exports with automatic codebooks
  • Wide format (one row per submission)
  • SPSS/SAS/R-ready column headers
  • Date range and completion filtering
  • CDISC-compatible XPT transport files
  • Data ownership: export and delete anytime
Real-Time Analytics

Clinical-Grade Statistics Dashboard

Monitor your study in real-time with live enrollment counters, completion tracking, and automated outlier detection.

  • Live enrollment and completion counters
  • N, mean, SD, median, IQR for numeric variables
  • Automated outlier detection (Z-score method)
  • Box plot visualizations
  • Completion rate tracking by questionnaire
  • Site-level performance comparison
Study Dashboard Preview

127

Enrolled

89%

Completion

Pain VAS (0-100)

N=127Mean: 42.3SD: 18.7
New Features

Recently Added Capabilities

We're constantly improving based on researcher feedback.

Data Query System

Raise data clarification queries with full audit trail

  • • Query by site or study level
  • • Priority levels (low to critical)
  • • Resolution workflow with notes
  • • Complete query audit log

Clinical Statistics

Publication-ready descriptive statistics

  • • Median, IQR, percentiles
  • • Z-score outlier detection
  • • Box plot visualizations
  • • Category frequency tables

Eligibility Pre-Screening

Automated qualification on landing pages

  • • Pre-screening questionnaires
  • • Automatic disqualification
  • • Custom thank-you messages
  • • Direct enrollment for qualified

Built for IRB Compliance

Technical infrastructure that supports regulatory requirements from day one.

HIPAA-Ready Infrastructure

AES-256 encryption, secure hosting

Comprehensive Audit Trails

Every action logged with timestamps

Role-Based Access Control

Granular permissions by user and site

Digital Consent Signatures

SHA-256 hashed, legally binding

21 CFR Part 11 Path

Electronic signatures and audit controls

GDPR Compliance

Right to erasure, data portability

We provide IRB documentation packages including security overviews, data handling procedures, and sample protocol language.

Grant Budget Planning Made Simple

Transparent pricing that fits academic budgets. Include in NIH, NSF, or foundation grants.

Free Sandbox

$0

Forever free

  • Unlimited study building
  • Simulated participants
  • Full feature access
  • IRB preparation
Most Popular

Live Studies

$19

per participant/month

  • Real data collection
  • Unlimited questionnaires
  • eConsent included
  • Email support

Enterprise

Custom

Large trials & institutions

  • Volume discounts
  • BAA included
  • CDISC exports
  • Dedicated support

Sample Budget Calculation

Study ParameterValue
Number of participants100
Study duration6 months
Cost per participant/month$19
Total data collection costs$11,400

Include in "Other Direct Costs" or "Contractual" budget categories. No setup fees.

Capture.Study vs REDCap

Both are great tools. Here's how we compare.

FactorCapture.StudyREDCap
Setup Time< 1 hour1-4 weeks
IT RequiredNoOften yes
Mobile ExperienceBuilt-in, optimizedRequires configuration
eConsentNative with signaturesLimited/add-on
Audit TrailAutomatic, cryptographicAvailable
PricingTransparent, $19/p/moFree + hidden costs
SupportDirect emailVaries by institution
Multi-SiteNativeComplex setup

Across Every Department

Academic researchers across disciplines use Capture.Study.

Psychology

Longitudinal mood and behavior studies

Nursing

Patient-reported outcomes research

Public Health

Community health behavior tracking

Medicine

Multi-center pilot trials

Kinesiology

Exercise adherence measurement

Start with Research-Ready Templates

100+ validated questionnaire and consent templates ready to customize.

Frequently Asked Questions

Everything academic researchers ask about Capture.Study.

Getting Started

IRB & Compliance

Pricing & Grants

Data & Exports

Participants

Comparison

Technical

Ready to Launch Your Academic Study?

Start building in the free sandbox today. No credit card, no sales calls, no IT required.

Browse Templates

No credit card required • IRB documentation included • Launch in under 1 hour