ClinicalTrials.gg
Active, not recruitingNCT07776834GenAI-HYPERUpdated Aug 20, 2026

Generative AI-Supported Personalized Education Compared With Printed Material for Adults With Hypertension

An interventional study of Standard Hypertension Education and Generative AI-Supported Personalized Hypertension Education in Hypertansion, sponsored by Akdeniz University. Active, not recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-20.

Sponsored by Akdeniz University · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
88
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

This study evaluates whether generative artificial intelligence-supported personalized education can improve hypertension knowledge and medication adherence in adults with hypertension compared with standard printed educational material. A total of 88 adults with hypertension are included in the study. Participants are assigned to either an intervention group or a control group. The control group receives a printed hypertension education booklet. The intervention group receives personalized educational content prepared using generative artificial intelligence based on individual characteristics and needs, together with weekly WhatsApp or SMS messages, voice messages, and brief telephone follow-up. The intervention lasts four weeks, and final assessments are performed in the fifth week. Hypertension knowledge, medication adherence self-efficacy, and blood pressure are assessed before and after the intervention. It is expected that personalized education will improve hypertension knowledge and medication adherence compared with printed education.

02

Conditions studied

  • Hypertansion

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Keywords

  • generative artificial intelligence
  • medication adherence
  • hypertansion
  • self efficacy
  • blood pressure
03

In context

Medication Adherence

937 studies on the registry are indexed under Medication Adherence; 159 are open to participants now.

This study's enrollment of 88 is below the median of 120 across 768 interventional studies indexed under Medication Adherence.

Browse Medication Adherence studies →

Lead sponsor

Akdeniz University is the lead sponsor of 297 studies on the registry; 62 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Voluntary agreement to participate in the study
  • Diagnosis of hypertension
  • Use of antihypertensive medication for at least 6 months
  • Medication adherence self-efficacy score of 26 or lower
  • Age 18 years or older
  • Ability to read and write in Turkish
  • General health status adequate for communication
  • Ability to read SMS messages and use WhatsApp

Exclusion criteria

Exclusion Criteria:

  • Withdrawal from the study after enrollment
  • Inability to be reached by telephone during the follow-up period
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
88 participants (actual)

Study arms

  • Active comparator
    control group

    Participants in this arm receive standard hypertension education and a printed hypertension education booklet. Baseline assessments and blood pressure measurements are performed in the first week. In the fifth week, post-intervention assessments and blood pressure measurements are repeated.

    Behavioral: Standard Hypertension Education

  • Experimental
    intervention group

    Participants in this arm receive generative artificial intelligence-supported personalized hypertension education based on their individual characteristics, needs, baseline information, and the standardized hypertension education content. The intervention is delivered over four weeks through weekly WhatsApp or SMS messages and voice messages. Brief structured telephone follow-up is conducted during the first and fourth weeks. In the fifth week, post-intervention assessments and blood pressure measurements are performed.

    Behavioral: Generative AI-Supported Personalized Hypertension Education

Interventions

  • BehavioralStandard Hypertension Education

    Participants receive standard hypertension education including medication-related information and a printed hypertension education booklet developed based on expert recommendations.

  • BehavioralGenerative AI-Supported Personalized Hypertension Education

    Participants receive personalized hypertension education generated using generative artificial intelligence based on individual characteristics, needs, baseline information, and standardized hypertension education content. The intervention is delivered over four weeks through weekly WhatsApp or SMS messages and voice messages. Brief structured telephone follow-up is provided in the first and fourth weeks.

06

What researchers measure

Primary outcomes

  1. Mean Change From Baseline in Medication Adherence Self-Efficacy Scale-Short Form (MASES-SF) Total Score at Week 5

    Medication adherence self-efficacy will be assessed using the 13-item Medication Adherence Self-Efficacy Scale-Short Form (MASES-SF). Each item is scored from 1 (not at all sure) to 4 (very sure), resulting in a total score ranging from 13 to 52. Higher scores indicate greater self-efficacy for adhering to antihypertensive medication. The change in total score from baseline to Week 5 will be evaluated.

    Time frame: Baseline and Week 5

  2. Mean Change From Baseline in Hypertension Knowledge-Level Scale (HK-LS) Total Score at Week 5

    Hypertension knowledge will be assessed using the 22-item Hypertension Knowledge-Level Scale (HK-LS). The scale includes six domains: definition, medical treatment, medication adherence, lifestyle, diet, and complications. Responses are recorded as true, false, or do not know, and each correct response receives 1 point. Higher scores indicate greater hypertension knowledge, and a score of 16 or above indicates a high level of hypertension knowledge. The change in total score from baseline to Week 5 will be evaluated.

    Time frame: Baseline and Week 5

Secondary outcomes

  1. Mean Change From Baseline in Systolic Blood Pressure at Week 5

    Systolic blood pressure will be measured in mmHg at baseline and Week 5. The change in systolic blood pressure from baseline to Week 5 will be evaluated.

    Time frame: Baseline and Week 5

  2. Mean Change From Baseline in Diastolic Blood Pressure at Week 5

    Diastolic blood pressure will be measured in mmHg at baseline and Week 5. The change in diastolic blood pressure from baseline to Week 5 will be evaluated.

    Time frame: Baseline and Week 5

07

Study locations

1 site
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jun 2026 (actual). Primary completion is estimated for Dec 2026, 6 months after the start.

Of 425 non-industry interventional studies with no phase under Medication Adherence, half reached primary completion within 22 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 42. This study's planned 6 months is below that.

Counting every sponsor, half of 442 studies reached it within 21 months; a quarter within 11 and three quarters within 41.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 18, 2026
First posted
Aug 20, 2026
StartActual
Jun 1, 2026
Primary completionEst.
Dec 20, 2026
CompletionEst.
Dec 20, 2026
Last update
Aug 20, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07776834
Lead sponsor
Akdeniz University
Responsible party
Sponsor
First posted
Aug 20, 2026
Start date
Jun 1, 2026
Primary completion
Dec 20, 2026 (estimated)
Completion
Dec 20, 2026 (estimated)
Last update
Aug 20, 2026

Study contacts

Yasemin DEMİR AVCI, PhD
principal investigator · Akdeniz University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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