Trial · NCT07890961
A Clinician-Patient Dual Behavior Change Framework to Leverage Informed Digital Nudges to Reduce Hospital Readmissions and Improve Patient Outcomes: A Trial for Scalable Strategy to Reduce Readmissions (PREVENT-R)
NCT07890961, Not applicable, Not yet recruiting, Yale University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. A Clinician-Patient Dual Behavior Change Framework to Leverage Informed Digital Nudges to Reduce Hospital Readmissions and Improve Patient Outcomes: A Trial for Scalable Strategy to Reduce Readmissions (PREVENT-R). Trials, record NCT07890961. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07890961
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
A Clinician-Patient Dual Behavior Change Framework to Leverage Informed Digital Nudges to Reduce Hospital Readmissions and Improve Patient Outcomes: A Trial for Scalable Strategy to Reduce Readmissions (PREVENT-R)
- NCT number
- NCT07890961
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 800 participants, estimated
- Lead sponsor
- Yale University
- Conditions
- Readmission, Readmission Rates, Readmission, Hospital, Elderly (People Aged 65 or More)
- Interventions
- Digital nudge prompting
- First posted
- 2026-10-23
- Last updated
- 2026-10-29
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Percentage of participants with hospital readmissions | 30 days following the index ED | Hospital readmission within 30 days of the index ED visit. |
| Secondary | Percentage of participants referred to the SNP | up to 3 months | Percentage of participants referred to the SNP to assess clinician referral behavior |
| Secondary | Percentage of participants that accept or decline SNP services | up to 3 months | Percentage of participants that accept or decline SNP services among those referred to and successfully contacted by the SNPt o assess patient acceptance |
| Secondary | Post-SNP assessment | up to 3 months | Patient-reported experience and outcomes will be assessed using the SNP survey administered at completion of SNP services. (This assessment is currently being refined.) |
| Secondary | Percentage of participants that interact with SNs | up to 3 months | Percentage of intervention arm participants that interact with SNs |
| Secondary | Percentage of participants that utilize services | up to 3 months | Percentage of intervention arm participants that utilized recommended services and supports. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants1
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years |
|---|---|---|---|---|---|
| P30AG024968 | USC-Yale Roybal Center for Behavioral Interventions in Aging | DOCTOR, JASON N.; MEEKER, DANIELLA | UNIVERSITY OF SOUTHERN CALIFORNIA | NATIONAL INSTITUTE ON AGING | 2004 to 2025 |
Source NIH RePORTER
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07890961
GET https://conductscience.org/api/trials/v1/NCT07890961/registered