NCT07506707

Brief Summary

The goal of this clinical trial is to learn whether a digital education program can help people with high blood pressure (hypertension) manage their condition better. The program aims to improve self-care behaviors and health literacy by teaching participants how to use digital tools, follow healthy lifestyle habits, and take their medicines regularly. Researchers will compare two groups. One group will receive digital education that includes short videos, brochures, and podcasts about blood pressure control and how to use online health platforms such as e-Nabız (Turkey's national e-health system). The other group will not receive this education. Participants will attend two sessions during two weeks. The main questions are: Does digital education improve self-care and e-health literacy in people with hypertension? Does it help participants take their medicine as prescribed and maintain healthy habits such as diet and exercise?

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
166

participants targeted

Target at P50-P75 for not_applicable hypertension

Timeline
1mo left

Started Apr 2026

Shorter than P25 for not_applicable hypertension

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress86%
Apr 2026May 2026

First Submitted

Initial submission to the registry

March 17, 2026

Completed
16 days until next milestone

First Posted

Study publicly available on registry

April 2, 2026

Completed
9 days until next milestone

Study Start

First participant enrolled

April 11, 2026

Completed
6 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 17, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

May 30, 2026

Expected
Last Updated

April 8, 2026

Status Verified

April 1, 2026

Enrollment Period

6 days

First QC Date

March 17, 2026

Last Update Submit

April 3, 2026

Conditions

Keywords

HypertensionDigital educationSelf-care behaviorsHealth literacye-Health literacyMedication adherence

Outcome Measures

Primary Outcomes (1)

  • Hypertension and E-Health Knowledge Level Score

    1. Change in Hypertension Self-Care Profile - Behavior Subscale score from baseline to 4 weeks post-intervention, with scores ranging from 11 (min) to 44(max), where higher scores indicate better hypertension self-care behavior. 2. Change in Hypertension Self- Care Profile - Motivation Subscale score from baseline to 4 weeks post-intervention, with scores ranging from 15 (min) to 60(max), where higher scores indicate better hypertension self-care motivation 3. Change in Hypertension Self Care Profile - Self Efficacy Subscale score from baseline to 4 weeks post-intervention, with scores ranging from 12 (min) to 48(max), where higher scores indicate better hypertension self-efficacy

    Week 1 (end of first session) and Week 4 (end of second session).

Secondary Outcomes (1)

  • E-Health System Proficiency Task Score

    Week 1 (end of first session) and Week 4 (end of second session).

Other Outcomes (1)

  • Blood Pressure Control (Systolic and Diastolic)

    Week 1 (end of first session) and Week 4 (end of second session).

Study Arms (2)

The group receiving Self-Care & E-Health (SC-EH) Training

EXPERIMENTAL

The study group consists of individuals aged 50 and older who are registered at the Bartın Life Center and meet the inclusion criteria, including those diagnosed with hypertension or taking antihypertensive medication. They will participate in an intervention program consisting of two sessions focused on hypertension self-management and e-health literacy.

Behavioral: Hypertension Self-Management and E-Health Education

The group not receiving Self-Care & E-Health (SC-EH) Training

NO INTERVENTION

The same scales will be administered to the control group without providing any training. Four weeks after the training provided to the experimental group, the control group will be given the training brochure.

Interventions

The education program consists of two sessions designed for hypertension management, combining self-care and e-health literacy.Each session is planned to last 15-20 minutes. The first session covers hypertension and healthy lifestyle changes (nutrition, exercise, stress management, etc.).The second session introduces e-health tools (digital blood pressure monitor apps, etc.) and systems like e-Nabız and MHRS, including practical demonstrations.The education is supported by visual-aided video narrations, plain-language brochures, sample screenshots, and live applications. Participants practically demonstrate logging into e-health systems and tracking data using their own mobile devices or provided digital tools. The intervention is conducted twice, once a week for two weeks. At the end of each session, knowledge and application skills are assessed through short evaluation questions. Post-education changes in individuals' hypertension management and e-health literacy levels are measured

Also known as: Integrated Self-Care and E-Health Literacy Training for Hypertension Management
The group receiving Self-Care & E-Health (SC-EH) Training

Eligibility Criteria

Age50 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Adults aged 50 years or older
  • Individuals with a clinical diagnosis of hypertension or those regularly using antihypertensive medication
  • Individuals actively registered at the Life Center and receiving regular services
  • Participants who provide written and verbal informed consent to voluntarily join the study
  • Individuals able to fully participate in the designated digital health education sessions
  • Participants capable of maintaining consistency throughout the intervention and follow up periods

You may not qualify if:

  • Individuals without a diagnosis of hypertension
  • Individuals unable to complete questionnaires or education sessions due to communication barriers or cognitive limitations
  • Illiterate individuals, as data collection requires reading and completing written questionnaires
  • Individuals unable to maintain participation or adhere to the follow up schedule during the study period

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

HypertensionMedication Adherence

Condition Hierarchy (Ancestors)

Vascular DiseasesCardiovascular DiseasesPatient CompliancePatient Acceptance of Health CareTreatment Adherence and ComplianceHealth BehaviorBehavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
No masking will be applied in this study. Both participants and researchers will be aware of group assignments due to the nature of the digital education intervention.
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: This study uses a randomized controlled, parallel-group, pre-test/post-test design to evaluate the effect of digital education on self-care behaviors and health literacy in adults with hypertension. Participants will be randomly assigned to either the intervention or control group. The intervention group will receive a structured two-session digital education program delivered over two weeks. The program includes short videos, brochures, and podcasts focusing on blood pressure management, medication adherence, lifestyle changes, and e-health literacy skills such as using digital tools like e-Nabız and MHRS. The control group will receive standard routine care without any digital training during the study. Both groups will complete pre- and post-intervention assessments using validated scales to measure self-care, e-health literacy, and medication adherence. Data will be analyzed to determine the effectiveness of the digital education model in improving hypertension self-management.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Prof. Dr. Ayfer Bayındır Çevik

Study Record Dates

First Submitted

March 17, 2026

First Posted

April 2, 2026

Study Start

April 11, 2026

Primary Completion

April 17, 2026

Study Completion (Estimated)

May 30, 2026

Last Updated

April 8, 2026

Record last verified: 2026-04