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05 · Library
Authoritative, plain-language guides on clinical trials — gathered from the NIH, ClinicalTrials.gov, the NCI, the FDA, and our own guides. Browse freely; sign in to save what’s useful to your dashboard.
Plain-language AI summaries pulled from trusted public sources (MedlinePlus, ClinicalTrials.gov). Not medical advice.
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37 resources
A free, ad-free platform for creating a private page to share health updates with family and friends and coordinate practical help through a treatment journey.
The NIH's plain-language hub on what clinical trials are, why people join, and what to expect — a trustworthy first stop if you're new to research studies.
The National Cancer Institute's guide to finding and joining cancer treatment trials, including how to search NCI-supported studies and questions to ask.
A National Cancer Institute guide to weighing a clinical trial — what to consider, questions to ask the study team, and how to think through risks, benefits, and logistics.
ClinicalMatchMate's own walkthrough of how to go from a diagnosis to a shortlist of trials worth asking your care team about, in plain language.
ClinicalTrials.gov's official primer on how studies are designed, what phases mean, and how eligibility works — the reference behind most trial listings you'll see.
The National Organization for Rare Disorders connects people affected by rare diseases to patient-assistance programs, plain-language education, and a network of member advocacy organizations.
A national nonprofit offering free case-management help with insurance appeals, medical debt, and co-payment relief for people in active treatment for serious illness.
A free, NIH-funded registry that helps connect people interested in research with studies that may be looking for volunteers. Joining is voluntary and you choose what to share.
How the public ClinicalTrials.gov registry works, what study information is posted, and how results are made available.
A national organization offering a round-the-clock helpline, patient programs like lodging and rides to treatment, plain-language information, and patient advocacy.
Free emotional and social support for anyone affected by cancer — a toll-free helpline, professionally led support groups, and local and online communities.
Free professional support and limited financial assistance for cancer-related costs such as transportation, home care, and co-payments, delivered by oncology social workers.
A free resource hub with checklists, toolkits, and a help desk for the family caregivers who support loved ones through illness and treatment.
The FDA's overview of the clinical-research stage of drug development: what each trial phase tests and the protections in place for the people who take part.
What inclusion and exclusion criteria are, why they exist, and how the study team confirms whether a trial is a fit — in plain language.
MedlinePlus gathers trusted, easy-to-read explainers on clinical trials from the National Library of Medicine, with links to related health topics in plain language.
Practical tools, education, and services for family caregivers, including condition-specific guidance and help locating local support.
The FDA's informed-consent resources for clinical investigations — what consent must explain and the protections it provides for people who take part in studies.
Common words you'll see in trial listings and consent forms — phase, placebo, randomization, adverse event — explained simply by ClinicalMatchMate.
A step-by-step National Cancer Institute guide to searching for treatment trials and understanding what the listings mean.
What informed consent really means: how the study team explains a trial, the document you'll review, and your right to ask questions and leave at any time.
How Medicare covers routine costs of qualifying clinical research studies, what is and isn't covered, and what to check before joining.
The National Alliance on Mental Illness offers free peer-led support groups, a helpline, and education for people navigating mental health alongside a medical condition.
A nonprofit directory of patient-assistance programs, free or low-cost clinics, and a drug discount card that helps people afford medicines and care.
What a Certificate of Confidentiality is and how it protects the privacy of people taking part in sensitive research by limiting disclosure of identifiable data.
Guidance from the federal Office for Human Research Protections on what informed consent requires and the rights it is meant to protect.
The federal office that oversees protections for people who take part in research, with plain-language explanations of your rights and how oversight works.
Who pays for what when you join a trial — which costs the study covers, what insurance may handle, and questions to ask the coordinator before you enroll.
What a placebo is, why some studies use one, when they don't, and what informed consent discloses — in plain language for patients and caregivers.
A plain-language checklist of questions for your care team and the study team — covering the study, risks and benefits, logistics, cost, and your rights.
The official search tool for the U.S. registry of clinical studies, where you can filter by condition, location, and recruitment status.
An online community where patients and caregivers learn from each other in condition-specific forums, including questions worth bringing to clinical-trial conversations.
Plain-language guidance from the National Cancer Institute on caring for someone in treatment while looking after your own wellbeing.
Free education and resources on health insurance, finances, employment rights, and disability for people navigating a cancer diagnosis.
A plain-language walkthrough of a typical trial schedule — screening, baseline, treatment-period visits, and follow-up — and how to plan around it.
How HIPAA protects your medical records, what rights you have to access and control your health information, and how to file a complaint.