Motivational Interviewing Effect on Reducing Cardiovascular Disease Risk Factors

Not Applicable

Active, not recruiting

• Conditions: Cardiovascular Diseases; Motivation; Risk Reduction; Nurse's Role
• Interventions: Other: motivational interviewing based training program; Other: Routine practice

• Registration Number: NCT06071351
• Lead Sponsor: Muş Alparlan University

Brief Summary

Aim: The aim of this study is to examine the effect of motivational interviewing-based training program on reducing cardiovascular disease risk factors in adults.

Methods: In the first stage, individuals' CVD risk levels were determined. In the second stage, a 6-session motivational interview-based training program was applied to the intervention group with a medium CVD risk level (HearthSCORE score between 2 and 5 points). Brochures were distributed to the control group.

Detailed Description

The aim of this study is to determine the CVD risks of adult individuals between the ages of 40-70 and to evaluate the effect of a motivational interview-based training program on reducing modifiable risk factors in individuals with moderate CVD risk.

Hypothesis; A 6-session motivational interview-based training program aimed at reducing CVD risk factors reduces the risk level in the intervention group more than the control group.

This study will be carried out in 2 stages. In the first phase, risk prevalence screening will be carried out to determine the CVD risks of individuals between October and November 2023. In the 2nd phase, a randomized controlled study will be conducted to evaluate the intervention program for individuals at medium risk level (HeartScore® between 2 and 5).

Study Timeline

• Study First Submitted: 2023-09-25
• Study Start: 2023-10-01
• Study First Submitted QC: 2023-10-04
• Study First Posted: 2023-10-06
• Status Verified: 2023-12
• Last Update Submitted: 2023-12-04
• Last Update Posted: 2023-12-05
• Primary Completion: 2024-03-20
• Study Completion: 2024-03-21

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• Being aged between 40 and 70 years,
• Being voluntary to participate in the study,

Exclusion Criteria

• Having a known and diagnosed CVD
• Not being voluntary to participate in the study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Experimental intervention group	motivational interviewing based training program	In addition to the informative brochure prepared by the researcher, a 6-session motivational interview-based training program will be given. The training program will include topics such as nutrition, physical activity, smoking and alcohol use.
Control Group	Routine practice	An informative brochure prepared by the researcher and traditional consultancy services will be provided.

Primary Outcome Measures

Name	Time	Method
change is CVD risk level	24 week	In the first phase of the research, the "HeartScore®" program will be used to determine the CVD risk levels of individuals. Thanks to this program, the CVD risk levels of individuals will be learned and primary protection will be provided. According to "HeartScore®", CVD risk is discussed in 4 categories.; * 10%, very high risk,; * 5% - \<10%, high risk, Medium risk between ≥2-\<5%, If \<1%, they are in the low risk category. As the score increases, the CVD risk level increases.

Secondary Outcome Measures

Name	Time	Method
Change in Physical Activity Level	24 week	Physical activity level was measured using the International Physical Activity Questionnaire Short Form (IPAQ).; Sitting 1.5 MET Walking 3.3 MET Moderate Intensity Physical Activity 4.0 MET Vigorous Physical Activity 8.0 MET Short form (7 questions); It provides information on time spent awake, moderate to vigorous intensity activities, and time spent sitting. The IPAQ categorically classifies individuals as "inactive," "minimally active," and "very active."

Trial Locations

Locations (1)

Kepez Devlet Hastanesi; 🇹🇷 Antalya, Turkey