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This study will utilize a three-phase approach that is informed by a theory-driven implementation framework to: 1) conduct a needs analysis in order to identify individual-, health care team-, and practice-level barriers and facilitators to conducting adherence counseling in safety-net primary care practices; 2) develop a virtual communication simulation designed to improve the quality of adherence counseling by allowing nurses repeated opportunities to practice discussing medication adherence with virtual patients; and 3) conduct a pilot study to evaluate the feasibility, acceptability and preliminary efficacy of the simulation on changes in: a) nurses' collaborative communication skills, b) medication adherence, and c) reduction in BP in a sample of 20 patients with uncontrolled hypertension (HTN) who are non-adherent to their medications.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Communication Simulation | Experimental | Nurses will use simulation over 12 weeks while fidelity is monitored using the NIH Behavior Change Consortium Treatment Fidelity Guidelines. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Audiotaped Counseling Session | Behavioral | Patients and nurses will complete audio taped counseling session at least 3 months following the baseline visit. Patients will rate quality of nurse communication skills |
| Measure | Description | Time Frame |
|---|---|---|
| Feasibility measured by documenting total available and eligible nurses and patients approached to enroll 1 participant through final study visit | 6 Months | |
| Acceptability measured by % of nurses who complete the simulation | 6 Months |
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Inclusion Criteria:
PCPs and nurses will be enrolled if they fulfill the following criteria:
No exclusions will be made based on provider race/ethnic origin. We will oversample males to examine differential communication skills based on gender.
Patient eligibility criteria include:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Antoinette Schoenthaler, MD | NYU Langone Health | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| NYU School of Medicine | New York | New York | 10016 | United States |
Individual participant data that underlie the results reported in this article, after deidentification (text, tables, figures, and appendices). Will be used for secondary data analysis approved by the investigator
Beginning 3 months and ending 5 years following article publication.
Researchers who provide a methodologically sound proposal.
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| ID | Term |
|---|---|
| D006973 | Hypertension |
| ID | Term |
|---|---|
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
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