--- title: Bronchopulmonary Dysplasia Prevention Study Consent Form Template | Paperform description: Professional research participation and consent form for BPD prevention studies in extremely preterm infants. Includes surfactant protocols, ventilation randomization, and respiratory outcome tracking for neonatal clinical trials. url: "https://paperform.co/templates/bronchopulmonary-dysplasia-prevention-study-consent-form" type: static generatedAt: "2026-04-04T00:43:19.990Z" --- [← Back to free form templates](/templates/) ![Bronchopulmonary Dysplasia Prevention Study Consent Form](https://img.paperform.co/fetch/f_webp/https://d3gw2uv1ch7vdq.cloudfront.net/content/form_templates/assets/bronchopulmonary-dysplasia-prevention-study-consent-form.png) [Preview](https://_preview.paperform.co/ai-template/bronchopulmonary-dysplasia-prevention-study-consent-form) [Use this template for free](/create?ai-template=bronchopulmonary-dysplasia-prevention-study-consent-form) [Discovery & Research Forms](/templates/category/discovery-research/)[Healthcare & Medical Forms](/templates/category/healthcare/) [Healthcare](/templates/industry/healthcare/) [Physician](/templates/role/physician/)[Nurse](/templates/role/nurse/)[Healthcare Administrator](/templates/role/healthcare-admin/)[Researcher](/templates/role/researcher/) About this free form template ### Bronchopulmonary Dysplasia Prevention Study: Research Participation & Consent Conducting clinical research on extremely preterm infants requires meticulous informed consent processes and careful data collection. This **Bronchopulmonary Dysplasia (BPD) Prevention Study Consent Form** is designed specifically for neonatal research teams, hospitals, and academic medical centers conducting trials on respiratory interventions for premature babies. #### Why This Template Works for Neonatal Research This form streamlines the complex process of enrolling extremely preterm infants (born before 28 weeks gestation) into BPD prevention studies. It guides parents and legal guardians through detailed study information, intervention protocols including surfactant administration and ventilation strategies, potential risks and benefits, and comprehensive consent documentation. The template is built for **neonatologists, clinical research coordinators, NICU teams, and pediatric researchers** who need to meet stringent IRB requirements while maintaining compassionate, clear communication with families during a highly stressful time. #### Integrated Workflows for Clinical Research Using Paperform's conditional logic, this form adapts based on gestational age, birth weight, and specific study arm randomization. When integrated with [Stepper](https://stepper.io), you can automate critical research workflows: trigger notifications to the research team when consent is obtained, update REDCap or other clinical trial databases automatically, schedule follow-up assessments, and maintain HIPAA-compliant audit trails. For studies requiring formal consent signatures, [Papersign](https://papersign.com) enables secure electronic signatures from both parents/guardians and witnessing staff members, creating legally binding consent documents that remain linked to the original enrollment data. #### Designed for Regulatory Compliance This template addresses the unique regulatory requirements of neonatal clinical trials, including detailed disclosure of experimental interventions, randomization procedures, data privacy protections, and withdrawal rights. The clear, accessible language helps research teams meet Good Clinical Practice (GCP) standards while ensuring families truly understand what study participation means for their vulnerable infant. Whether you're conducting single-center pilots or multi-site randomized controlled trials, this form provides the foundation for ethical, compliant, and efficient participant enrollment in critical neonatal respiratory research. 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