Reference
Clinical Trial Patient Recruitment App glossary
Terms used in Clinical Trial Patient Recruitment App and its documentation.
Applies to Clinical Trial Patient Recruitment App as it works today. Moraph updates the platform continuously, and this page is reviewed when it changes.
Terms used in Clinical Trial Patient Recruitment App and its documentation.
| Term | Meaning |
|---|---|
| Pre-screening | A short, IRB-approved questionnaire a prospective participant completes before the site contacts them. It does not decide eligibility. |
| Referral | A record of a prospective participant passed to the site from pre-screening or an outreach source. |
| Consent version | A specific IRB-approved version of the consent materials. Each signature is tied to one version. |
| Countersignature | The investigator or designee's confirmation that the consent discussion took place. |
| Reconsent | Signing a newly approved consent version after a protocol or consent amendment. |
| Schedule of activities | The protocol's list of visits and tasks, used to build reminders. |
| Participant report | A symptom, new medicine or hospital visit reported by a participant between visits, assessed by the investigator. |
| Coded data | Data identified by a study participant identifier rather than name, as shown to sponsors by default. |
| Delegation log | The site's record of which staff are delegated which study tasks, used to set roles. |
| Reference prefix | The capital letters at the start of a record reference, such as PTCP in PTCP-4M8QZ2. |
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