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Motivational Interviewing Effect on Reducing Cardiovascular Disease Risk Factors

M

Muş Alparlan University

Status

Active, not recruiting

Conditions

Motivation
Cardiovascular Diseases
Risk Reduction
Nurse's Role

Treatments

Other: motivational interviewing based training program
Other: Routine practice

Study type

Interventional

Funder types

Other

Identifiers

NCT06071351
07/07/2023- 7/51

Details and patient eligibility

About

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.

Full 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).

Enrollment

40 estimated patients

Sex

All

Ages

40 to 70 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

Experimental intervention group
Experimental group
Description:
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.
Treatment:
Other: motivational interviewing based training program
Control Group
Active Comparator group
Description:
An informative brochure prepared by the researcher and traditional consultancy services will be provided.
Treatment:
Other: Routine practice

Trial contacts and locations

1

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Central trial contact

Hasan EVCİMEN, PhD

Data sourced from clinicaltrials.gov

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