Health Belief Model-Based Telenursing for Hypertension
The Effect of Health Belief Model-Based Interventions Delivered Via Telenursing to Individuals Diagnosed With Hypertension on Hypertension Self-Efficacy and Quality of Life
1 other identifier
interventional
78
1 country
1
Brief Summary
This randomized controlled trial evaluated the effects of a Health Belief Model-based telenursing intervention on self-efficacy, quality of life, blood pressure, body mass index, and health behaviors in individuals with hypertension. A total of 78 participants were randomly assigned to the intervention group (n=39) or control group (n=39). Participants in the intervention group received a 12-week telenursing intervention based on the Health Belief Model, including face-to-face education, training on home blood pressure monitoring, educational materials, weekly text messages, and telephone follow-up at weeks 2, 4, 8, and 12. The control group received usual care. Outcomes were assessed at baseline, 3 months, and 6 months.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable hypertension
Started Jul 2024
Shorter than P25 for not_applicable hypertension
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 9, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 28, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
February 28, 2025
CompletedFirst Submitted
Initial submission to the registry
September 11, 2026
CompletedFirst Posted
Study publicly available on registry
September 16, 2026
CompletedSeptember 16, 2026
September 1, 2026
8 months
September 11, 2026
September 11, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Hypertension Self-Efficacy
Hypertension self-efficacy was assessed using the Hypertension Self-Efficacy Scale (HSES). The scale consists of 20 items, with higher scores indicating higher hypertension self-efficacy.
Baseline, 3 months, and 6 months
Health-Related Quality of Life
Health-related quality of life was assessed using the 12-Item Short Form Health Survey (SF-12), which provides Physical Component Summary (PCS) and Mental Component Summary (MCS) scores. Higher scores indicate better health-related quality of life.
Baseline, 3 months, and 6 months
Secondary Outcomes (3)
Systolic Blood Pressure
Baseline, 3 months, and 6 months
Diastolic Blood Pressure
Baseline, 3 months, and 6 months
Body Mass Index
Baseline, 3 months, and 6 months
Study Arms (2)
Intervention Group
EXPERIMENTALParticipants received a 12-week Health Belief Model-based telenursing intervention in addition to routine care. The intervention included education, telephone follow-up, and weekly text messages.
Control Group
NO INTERVENTIONParticipants received routine care without the Health Belief Model-based telenursing intervention. Outcome assessments were conducted at baseline, 3 months, and 6 months.
Interventions
The intervention consisted of Health Belief Model-based education and a 12-week telenursing follow-up program. Participants received four telephone follow-up calls at weeks 2, 4, 8, and 12, each lasting approximately 10-15 minutes. Weekly text messages were sent for 12 weeks to remind participants about blood pressure monitoring and to provide information about hypertension management. Participants could also contact the researcher when they needed additional support.
Eligibility Criteria
You may qualify if:
- Aged 30-65 years
- Diagnosed with hypertension by a physician
- No cognitive or hearing impairments that could hinder communication
- Literate
- Using a mobile phone
- Willing to participate in the study
You may not qualify if:
- Did not respond to scheduled telephone calls for at least two consecutive weeks
- Transferred registration to another Family Health Center
- Voluntarily withdrew from the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Zümrütevler 2 No'lu Aile Sağlığı Merkezi
Istanbul, 34852, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Masking Details
- Participants were not informed whether they were assigned to the intervention or control group.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 11, 2026
First Posted
September 16, 2026
Study Start
July 9, 2024
Primary Completion
February 28, 2025
Study Completion
February 28, 2025
Last Updated
September 16, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share