Clinical Trials Directory

Trials / Completed

CompletedNCT06490575

Using Nonpharmacological Approaches in Hypertension Prevention and Management

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Kansas State University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The goal of this randomized controlled trial is to test the effectiveness of a four-module nutrition education resource promoting nonpharmacological approaches to prevent and manage hypertension. The main questions it aims to answer are: * Does the educational intervention increase the knowledge of using nonpharmacological approaches in preventing and managing hypertension among participants? * Does the educational intervention improve participants' lifestyle behaviors to prevent and manage hypertension? Researchers will compare a four-module educational intervention with a control group (no educational information received until after the study) to see if the educational intervention works to improve knowledge and healthy lifestyle behaviors in preventing and managing hypertension. Participants will: * Attend a 30-minute workshop every week for 4 weeks or no workshop at all * Complete a survey on demographic information, knowledge, lifestyle behaviors, and quality of life at baseline and end of the study * Complete a dietary 24-hour food recall at baseline, two weeks into the study, and at the end of the study * Monitor blood pressure levels two times a day for four weeks

Detailed description

Study Design: This study is a randomized controlled trial with 30 participants randomly divided into control (n=15) and intervention (n=15) groups. Pre- and post-survey Assessment: All participants completed a comprehensive self-administered survey at baseline, which included: * Knowledge related to hypertension and its management * Lifestyle behaviors (diet, physical activity, alcohol intake, smoking status) * Quality of life metrics * Constructs from the Protection Motivation Theory (PMT), such as response efficacy, self-efficacy, perceived vulnerability, perceived severity, and intention Dietary Assessment: The Automated Self-Administered 24-hour Dietary Assessment Tool (ASA24) was used to assess participants' intake of fruits, vegetables, dietary sodium, and dietary potassium at three points: * Baseline * Mid-program (two weeks into the intervention) * Post-intervention Intervention: The intervention group attended four weekly workshops, each lasting 30 minutes. The workshops were designed and led by a public health nutrition doctoral student and a nutrition expert. Each session included: * Presentations with PowerPoint slides and interactive activities * Group discussions * Questions and answers * Distribution of educational pamphlets and booklets The educational sessions focused on: * Increasing knowledge about hypertension prevention and management * Promoting nonpharmacological approaches to prevent and manage hypertension, such as dietary changes and lifestyle modifications * Addressing PMT components to influence participants' beliefs and intentions regarding their health behaviors Control Group: Participants in the control group did not receive any educational or counseling sessions during the intervention period. After the post-intervention survey, they were provided with all the educational materials and a brief overview of the contents. Data Analysis: Data collected from the surveys and ASA24 dietary assessments were analyzed using the Statistical Package for the Social Sciences (SPSS). Analyses focused on comparing changes in knowledge, lifestyle behaviors, quality of life, and dietary intake between the control and intervention groups.

Conditions

Interventions

TypeNameDescription
OTHEREducational Intervention Based on Protection Motivation Theory to Improve Knowledge and Promote Nonpharmacological Approaches to Prevent and Manage Hypertension among AdultsParticipants in the intervention group attended four face-to-face workshops (one session per week). Each session took about 30 minutes and consisted of lectures with PowerPoint presentations, discussion, questions and answers, and the distribution of educational pamphlets and booklets.

Timeline

Start date
2020-12-18
Primary completion
2022-06-20
Completion
2023-02-20
First posted
2024-07-08
Last updated
2024-07-08

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06490575. Inclusion in this directory is not an endorsement.