Clinical trial · Interventional
Personal Web Page In Clinical Trial Participant Education
Use of a Video-based, Personalized Web Page as a Complement to Standard Patient Education for Clinical Trial Participants
NCT03887091CI-TRIAL-00038976completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This research study is evaluating the effectiveness of video and web-based communication in clinical research compared to standard practices.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Genitourinary Cancer | Malignant Genitourinary System Neoplasm | ALIAS | 0.90 |
| Kidney Cancer | Malignant Kidney Neoplasm | CURATED_EXACT | 0.92 |
| Prostate Cancer | Malignant Prostate Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Postwire | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Postwire© Virtual Education Cohort
- description
- * Participants will be administered a brief questionnaire that asks questions about participant internet access, use, and understanding (Appendix B). This questionnaire will be used to determine eligibility. * In randomized into the Virtual Education Cohort:A video based, personalized web page will be created that has information related to the participants therapeutic clinical trial. * This web page will have videos of a research nurse explaining how to take study medication(s), how to fill out the study drug diary, and a description of the main side effects associated with the study drugs. * Clinic Visit Video Recording Cycle 1-4/Day 1 * Participants from both groups will be asked to complete two surveys before each Day 1 clinic visit for Cycles 1-7
- interventionNames
- Other: Postwire
- type
- NO_INTERVENTION
- label
- No Video Intervention
- description
- Participants will be administered a brief questionnaire that asks questions about participant internet access, use, and understanding (Appendix B). This questionnaire will be used to determine eligibility * Participants randomized to the control cohort will follow standard of care procedures involving clinic visits that do not include the use of video or access to a personalized web page. * Participants from both groups will be asked to complete two surveys before each Day 1 clinic visit for Cycles 1-7.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
* Participants must be ≥ 18 years of age * Participants must have an advanced or metastatic genitourinary malignancy (prostate or kidney cancer) * Participants must be consented to one of the selected clinical trials (see Appendix A) * Participants must be able to read and write English * Participants must have access to the internet at a minimum of once per week * Participants must use the internet at a minimum of once per week * Participants must feel at least somewhat confident in how to use the internet, as determined by the eligibility questionnaire to be completed by the participant
References
Publications (0)
Data not yet available
No reference posted for this study.