Trial · NCT07914452
Personalized Routine and Habit Integration to Support Medication Management
NCT07914452, Not applicable, Not yet recruiting, Brigham and Women's Hospital
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. Personalized Routine and Habit Integration to Support Medication Management. Trials, record NCT07914452. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07914452
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Personalized Routine and Habit Integration to Support Medication Management
- NCT number
- NCT07914452
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 100 participants, estimated
- Lead sponsor
- Brigham and Women's Hospital
- Conditions
- Medication Adherence
- Interventions
- PRISM Arm, Enhanced Usual Care Arm
- First posted
- 2026-11-03
- Last updated
- 2026-11-03
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | PDC (Continuous) - Cardiometabolic | Through 6-months post-baseline | Medication adherence to cardio-metabolic pill-form daily medications including the following classes: ACE inhibitor, Angiotensin Receptor Blockers (ARBs), Beta-Blockers, Calcium Channel Blockers, Diuretics, Lipid-lowering, Metformin |
| Secondary | PDC (Continuous) - All | Through 6-months post-baseline | Medication adherence to all daily prescription pill-form medications |
| Secondary | PDC (Continuous) - Study-entering | Through 6-months post-baseline | Medication adherence to study-entering medication i.e. the medciation that was identified during the eligibility screening process as having poor medication adherence. |
| Secondary | Medication Adherence Report Scale 10-item (MARS-10) | Through 3-months post-baseline | Self reported; medication ahderence to all prescriptoin daily medications |
| Secondary | Regimen Knowledge (continuous) | Through 3-months post-baseline | Participant knowledge of prescribed medications, including their purpose, dosage, and administration instructions using Medication Purpose \& Dosage Identification Score (MPDS). |
| Secondary | Regimen Complexity (continuous) | Through 3-months post-baseline | Complexity of the participant's prescribed medication regime using Medication Regimen Complexity Index (MRCI). |
| Secondary | Daily Routine (continuous) | Through 3-months post-baseline | Daily activity patterns and routines, including the timing of activities throughout the day using a time diary. |
| Secondary | Medication Habits (continuous) | Through 3-months post-baseline | The extent to which medication-taking is performed automatically as a habitual behavior using Self-Report Behavioral Automaticity Index (SRBAI). |
| Secondary | Problem Solving Skills (continuous) | Through 3-months post-baseline | Participant ability to identify, address, and learn from problems affecting medication-taking and health management using Health Problem-Solving Scale (HPSS). |
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 |
|---|---|---|---|---|---|
| P30AG064199 | The Roybal Center for Therapeutic Optimization using Behavioral Science | LAUFFENBURGER, JULIE CHRISTINE | BRIGHAM AND WOMEN'S HOSPITAL | NATIONAL INSTITUTE ON AGING | 2019 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/NCT07914452
GET https://conductscience.org/api/trials/v1/NCT07914452/registered