Digital Education for Hypertension Management: Effects on Self-Care and Health Literacy
DIGIHYPE-HTN
Digital Education Approach in Hypertension Management: Its Effect on Self-Care Behaviors and Health Literacy
1 other identifier
interventional
166
0 countries
N/A
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable hypertension
Started Apr 2026
Shorter than P25 for not_applicable hypertension
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
First Submitted
Initial submission to the registry
March 17, 2026
CompletedFirst Posted
Study publicly available on registry
April 2, 2026
CompletedStudy Start
First participant enrolled
April 11, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 17, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 30, 2026
ExpectedApril 8, 2026
April 1, 2026
6 days
March 17, 2026
April 3, 2026
Conditions
Keywords
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
EXPERIMENTALThe 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.
The group not receiving Self-Care & E-Health (SC-EH) Training
NO INTERVENTIONThe 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
Eligibility Criteria
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
Condition Hierarchy (Ancestors)
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
- 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