All terms in NCIT
| Label | Id | Description |
|---|---|---|
| RFM Mouse | NCIT_C14682 | |
| Overall Experience Participating in Research Study | NCIT_C125456 | [A question about an individual's experience while participating in a research study.] |
| RF/J Mouse | NCIT_C14683 | |
| One Thing to Improve Experience Participating in Research Study | NCIT_C125457 | [A question about the one thing an individual would recommend to improve their experience participating in a research study.] |
| NZB/BINJ X RF/J R and C Wimer, 1981 | NCIT_C14684 | |
| Talk with Someone about Concerns | NCIT_C125458 | [A question about whether an individual would like to talk to someone about their concerns.] |
| SZA Mouse | NCIT_C14685 | |
| Was It Worth It Questionnaire | NCIT_C125451 | [A questionnaire designed to measure a patient's opinion of their participation in a phase II or III treatment trial and their decision making regarding treatment.] |
| SZB Mouse | NCIT_C14686 | |
| Worthwhile to Participate in Research Study | NCIT_C125452 | [A question about whether an individual thinks it was worthwhile to participate in a research study.] |
| SZC Mouse | NCIT_C14687 | |
| Would Participate in Research Study Again | NCIT_C125453 | [A question about whether an individual would participate in a research study again.] |
| Rockefeller Inst, Heterogeneous Stock, R Strain | NCIT_C14688 | |
| Recommend Participating in Research Study to Others | NCIT_C125454 | [A question about whether an individual would recommend participation in a research study.] |
| SC Mouse | NCIT_C14689 | |
| Clinical Trial Coordinating Investigator Documentation | NCIT_C125426 | [Documentation from a coordinating investigator on a clinical trial.] |
| Clinical Trial Investigator Site Documentation | NCIT_C115654 | [Records pertaining to an investigator site in a clinical trial.] |
| Clinical Trial Subject Eligibility Verification Form and Worksheet | NCIT_C125427 | [Clinical trial documents used to ensure a subject is an appropriate candidate to participate in a clinical study, as outlined in the study protocol.] |
| BSVS | NCIT_C14690 | |
| Clinical Trial Ongoing Third Party Oversight Document | NCIT_C125428 | [Documents attesting that a third party continues to meet all relevant criteria to fulfill a contractual obligation in a clinical trial.] |