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Training in the 21st Century: Using Virtual Role-Plays to Improve Nurse Communication for Medication Adherence

NYU Langone Health logo

NYU Langone Health

Status

Completed

Conditions

Hypertension
High Blood Pressure

Treatments

Behavioral: Audiotaped Counseling Session

Study type

Interventional

Funder types

Other

Identifiers

NCT03599050
18-01003

Details and patient eligibility

About

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.

Enrollment

26 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • PCPs and nurses will be enrolled if they fulfill the following criteria:

    1. male or female healthcare provider (MD/DO, NP, and Registered Nurse) practicing at the clinic
    2. age 18 years or older.

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:

    1. receiving care at the participating clinic
    2. having uncontrolled HTN (BP>140/90 mmHg) at two visits in the past year
    3. being prescribed at least one antihypertensive medication and are non-adherent
    4. are ≥age 18 years
    5. fluent in English

Exclusion criteria

  • Unable to give consent
  • Have a diagnosis of cognitive dysfunction or significant psychiatric comorbidity,
  • Participating in another HTN-related study.

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

26 participants in 1 patient group

Communication Simulation
Experimental group
Description:
Nurses will use simulation over 12 weeks while fidelity is monitored using the NIH Behavior Change Consortium Treatment Fidelity Guidelines.
Treatment:
Behavioral: Audiotaped Counseling Session

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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