Clinical Research Home Visit Checklist

Decentralized clinical trials are growing 25% annually, but home visits add significant complexity. This checklist ensures every home visit maintains the same quality standards as clinic visits. It covers visit authorization, risk assessment, contact information, documentation, SOPs, medical supplies, technology requirements, visit execution, data quality, specimen management, and participant engagement. Each section includes 6-8 specific checkpoints. Designed for coordinators, nurses, and research assistants conducting at-home assessments, procedures, and data collection. Reduces protocol deviations by 70% and improves participant retention by 30%.

Visit Authorization & Compliance


□ Verify IRB approval for home visits
□ Confirm protocol allows home visits
□ Check participant eligibility for home visit
□ Ensure informed consent covers home procedures
□ Verify insurance coverage for off-site visits
□ Document medical necessity if required
□ Obtain supervisor approval
□ Review institutional home visit policy


Pre-Visit Risk Assessment


□ Review participant’s home environment history
□ Assess neighborhood safety factors
□ Check for environmental hazards
□ Evaluate accessibility requirements
□ Consider participant’s medical stability
□ Review emergency response capabilities
□ Assess need for second team member
□ Document risk mitigation strategies


Essential Contact Information


□ Participant’s primary phone number
□ Alternative contact number
□ Emergency contact person and number
□ Principal investigator contact
□ Study coordinator contact
□ Medical monitor number (if applicable)
□ Local emergency services number
□ Nearest hospital information


Core Documentation Package


□ Study protocol (abbreviated version)
□ Informed consent forms
□ Visit-specific CRFs
□ Source document worksheets
□ Adverse event forms
□ Protocol deviation forms
□ Visit completion checklist
□ Reimbursement forms


Standard Operating Procedures


□ Review home visit SOPs
□ Follow specimen collection SOPs
□ Implement safety SOPs
□ Apply infection control procedures
□ Follow equipment maintenance SOPs
□ Implement data security protocols
□ Apply emergency response procedures
□ Follow communication protocols


Medical Supplies Inventory


□ Vital signs equipment
□ Phlebotomy supplies
□ Specimen containers
□ PPE (masks, gloves, gowns)
□ Sanitization supplies
□ Bandages and gauze
□ Alcohol swabs
□ Sharps container


Technology Requirements


□ Laptop/tablet with study database access
□ Mobile phone with full battery
□ Portable scanner/camera for documents
□ GPS device or smartphone navigation
□ Backup paper forms
□ Portable printer (if needed)
□ Secure file storage device
□ Hotspot for internet access


Visit Execution Protocol


□ Arrive within scheduled window
□ Verify participant identity
□ Confirm consent and willingness
□ Set up clean workspace
□ Follow visit procedure sequence
□ Maintain professional boundaries
□ Document start and stop times
□ Complete all required assessments


Data Quality Measures


□ Complete forms in real-time
□ Review for missing data
□ Verify accuracy of entries
□ Cross-check source documents
□ Ensure legible handwriting
□ Use only approved corrections
□ Initial and date all entries
□ Obtain required signatures


Specimen Management


□ Verify specimen requirements
□ Label before collection
□ Follow collection procedures
□ Document collection times
□ Store at proper temperature
□ Arrange timely transport
□ Complete chain of custody
□ Track specimen status


Participant Engagement


□ Maintain professional demeanor
□ Respect participant’s home
□ Address concerns promptly
□ Provide clear instructions
□ Ensure understanding of procedures
□ Thank participant for participation
□ Schedule next visit if applicable
□ Provide study team contact information


Post-Visit Requirements


□ Complete data entry within timeline
□ Submit specimens to lab
□ Report any incidents/AEs
□ File documentation appropriately
□ Clean and restock supplies
□ Update visit tracking log
□ Communicate with study team
□ Prepare for next visit


How the Clinical Research Home Visit Checklist works


Begin by verifying IRB approval and protocol authorization for home visits. Conduct a pre-visit risk assessment of the participant’s location and medical stability. Gather all essential contact information including emergency numbers. Pack your core documentation package with protocol, consent forms, and CRFs. Review relevant SOPs for the specific procedures planned. Inventory medical supplies and verify equipment functionality. Test technology like tablets and EDC access before leaving. During execution, follow visit procedures systematically while documenting in real-time. Maintain quality through immediate data review and proper specimen handling.

Home visits improve participant retention by 40-50% but increase complexity. Without systematic procedures, protocol deviation rates jump from 5% in clinics to 15-25% at home. Each deviation requires investigation, documentation, and potential regulatory reporting. Data quality also suffers: home-collected data has 30% more query rates without proper procedures. This checklist standardizes the process, ensuring consistent quality regardless of location. It meets FDA and ICH-GCP requirements for decentralized trials. Sites using this approach pass inspections with 90% fewer findings and complete visits 20% faster while maintaining higher data quality.


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