Evaluating the Effect of an Evidence-Based One Page With Supplemental Visual Aids on the Knowledge and Perceptions of Blood Pressure Management Among Adults With Hypertension

• Sponsor: University of New Mexico (Other)
• Overall Status: Completed
• CT.gov ID: NCT04824560
• Collaborator: University of Missouri-Columbia (Other)
• Enrollment: 17
• Location: 1
• Arm: 1
• Actual Duration (Months): 5
• Patients Per Site Per Month: 3.4

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate changes in patient knowledge of blood pressure management and perceptions of making lifestyle changes to manage their blood pressure after implementation of an evidence-based one-page teaching protocol with supplemental handouts and optional use of suggested apps and web sites.

Condition or Disease	Intervention/Treatment	Phase
Hypertension	Behavioral: Blood pressure education	N/A

Study Design

• Study Type: Interventional
• Actual Enrollment: 17 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Masking: None (Open Label)
• Primary Purpose: Health Services Research
• Official Title: Evaluating the Effect of an Evidence-Based One Page With Supplemental Visual Aids on the Knowledge and Perceptions of Blood Pressure Management Among Adults With Hypertension
• Actual Study Start Date: Oct 1, 2020
• Actual Primary Completion Date: Mar 1, 2021
• Actual Study Completion Date: Mar 1, 2021

Arms and Interventions

Arm	Intervention/Treatment
Other: BP Education All participants enrolled receive blood pressure education.	Behavioral: Blood pressure education; One page teaching protocol performed by pharmacy students; phone follow-up

Outcome Measures

Primary Outcome Measures

1. Pre & Post Survey & Knowledge Test [8 weeks]

   change in participant's knowledge of blood pressure management - as measured by a pre- and post-test of 10 multiple-choice questions Change in participant's perception of making lifestyle changes to manage their hypertension - measured via pre- and post-survey using a 1-5 Likert Scale rating usefulness of the program and educational resources provided; and questions about which lifestyle modifications were made by the participant, which apps were used by the participant (if applicable), and which educational handouts were used by the participant

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 75 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• Adults from 18 to 75 years old

• Ability to self-consent

• English-speaking

• Able to read/write English

• Currently prescribed at least one medication for treatment of essential primary hypertension

Exclusion Criteria:

• Adults unable to consent

• Individuals who are not yet adults (infants, children, teenagers)

• Pregnant women

• Prisoners

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Walgreens Store #6587	Albuquerque	New Mexico	United States	87112

Sponsors and Collaborators

• University of New Mexico
• University of Missouri-Columbia

Investigators

None specified.

Study Documents (Full-Text)

• Informed Consent Form - Jun 12, 2020

More Information

Publications

None provided.

• Responsible Party: University of New Mexico
• ClinicalTrials.gov Identifier: NCT04824560
• Other Study ID Numbers: 20-458
• First Posted: Apr 1, 2021
• Last Update Posted: Apr 1, 2021
• Last Verified: Aug 1, 2020

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Hypertension

Study Results

No Results Posted as of Apr 1, 2021