Nurse-Led Motivational Interviewing for Blood Pressure Control

ConditionHypertension
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorKutahya Health Sciences University

About this trial

Hypertension is one of the most important risk factors for cardiovascular morbidity and mortality. Effective hypertension management requires medication adherence, lifestyle modification, regular blood pressure monitoring, and self-management behaviors. Motivational interviewing is a counseling approach that may support behavior change and improve hypertension management.

This study aims to evaluate the effects of nurse-led individual motivational interviewing and family-involved motivational interviewing on blood pressure control in patients with hypertension. The study will be conducted as a single-center, three-arm, parallel-group, randomized controlled trial. A total of 180 patients with hypertension will be randomly assigned to one of three groups: usual care, individual motivational interviewing, or family-involved motivational interviewing.

Participants in the intervention groups will receive a 6-week nurse-led motivational interviewing program. In the family-involved motivational interviewing group, a family member who supports hypertension management will also participate in the sessions. Data will be collected at baseline, 6 weeks, and 18 weeks. The primary outcome is systolic blood pressure. Secondary outcomes include diastolic blood pressure, hypertension knowledge level, treatment adherence, and hypertension self-efficacy.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Aged 18 years or older

Diagnosed with hypertension for at least 6 months

Using antihypertensive medication

Able to read and understand Turkish

Disqualifiers

Advanced cognitive impairment

Active psychiatric crisis

History of a serious cardiovascular event within the last 3 months

Terminal illness

Trial design

Design model

Parallel

Treatments tested in this trial

  • Individual Motivational Interviewing

    Behavioral

    The intervention is a structured 6-week nurse-led individual motivational interviewing program. Sessions will focus on hypertension awareness, individual risk factors, readiness for change, hypertension knowledge, misconceptions and complications, medication adherence, treatment barriers, salt reduction, nutrition behaviors, home blood pressure monitoring, physical activity, weight control, stress management, self-efficacy, problem solving, motivation maintenance, and individualized goal evaluation.

  • Family-Involved Motivational Interviewing

    Behavioral

    The intervention is a structured 6-week nurse-led motivational interviewing program delivered with the participation of a family member who supports the patient's hypertension management. The intervention content is the same as the individual motivational interviewing program. The family member will be included to support medication adherence, salt reduction, nutrition behaviors, home blood pressure monitoring, and achievement of weekly goals.

  • Usual Hypertension Care With Information Brochure

    Behavioral

    Participants will continue to receive routine hypertension care and will be given a standard hypertension information brochure. No structured motivational interviewing session will be provided.

Treatment groups

180 Participants
are divided into 3 treatment groups
Group A: Usual Hypertension Care With Information BrochureActive comparator 1 intervention
Group B: Nurse-Led Individual Motivational InterviewingExperimental treatment 1 intervention
Group C: Nurse-Led Family-Involved Motivational InterviewingExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Systolic Blood Pressure

Systolic blood pressure will be measured in mmHg using a standard blood pressure measurement procedure. Measurements will be taken after at least 5 minutes of rest using an appropriate cuff. At each assessment, at least two measurements will be taken from the same arm, and the average value will be used in the analysis. Lower systolic blood pressure values indicate better blood pressure control.

Time frame
Baseline, 6 weeks, and 18 weeks

Secondary outcomes

1

Diastolic Blood Pressure

Diastolic blood pressure will be measured in mmHg using a standard blood pressure measurement procedure. Measurements will be taken after at least 5 minutes of rest using an appropriate cuff. At each assessment, at least two measurements will be taken from the same arm, and the average value will be used in the analysis. Lower diastolic blood pressure values indicate better blood pressure control.

Time frame
Baseline, 6 weeks, and 18 weeks
2

Hypertension Knowledge Level Assessed by the Hypertension Knowledge-Level Scale

Hypertension knowledge level will be assessed using the Hypertension Knowledge-Level Scale. The scale includes 22 items. Total scores range from 0 to 22. Higher scores indicate a higher level of hypertension-related knowledge.

Time frame
Baseline, 6 weeks, and 18 weeks
3

Treatment Adherence Assessed by the Hill-Bone Hypertension Treatment Adherence Scale

Treatment adherence will be assessed using the Hill-Bone Hypertension Treatment Adherence Scale. The scale includes 12 items. Total scores range from 12 to 48. Higher scores indicate poorer adherence to hypertension treatment, while lower scores indicate better treatment adherence.

Time frame
Baseline, 6 weeks, and 18 weeks
4

Hypertension Self-Efficacy Assessed by the Hypertension Self-Efficacy Scale

Hypertension self-efficacy will be assessed using the Hypertension Self-Efficacy Scale. The scale includes 20 items. Total scores range from 20 to 80. Higher scores indicate higher hypertension self-efficacy.

Time frame
Baseline, 6 weeks, and 18 weeks

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.