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Effect of a Web-based Application With Integrated AI Chat for Cardiovascular Risk Support

NCT07917000, Not applicable, Not yet recruiting, Cairo University

Trial 10

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleEffect of a Web-based Application With Integrated AI Chat for Cardiovascular Risk SupportClinicalTrials.gov
NCT numberNCT07917000ClinicalTrials.gov
StatusNot yet recruitingClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment116 participants, estimatedClinicalTrials.gov
Lead sponsorCairo UniversityClinicalTrials.gov
ConditionsAI Chatbot, Cardiovascular (CV) RiskClinicalTrials.gov
Interventionsweb application with AI chat, usual clinic care follows the national prevention and management guidelines for major cardiovascular risk factorsClinicalTrials.gov
First posted2026-11-04ClinicalTrials.gov
Last updated2026-11-04ClinicalTrials.gov

Registered outcomes 9

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryMean absolute change in predicted 10-year cardiovascular risk (%) from baseline to 3 months in intervention and control groups.3 monthsClinicalTrials.gov
SecondaryMean change in systolic BP (mmHg)3 monthsChange in systolic blood pressure from baseline to 3 months, measured in mmHg.ClinicalTrials.gov
SecondaryMean change in diastolic blood pressure3 monthsChange in diastolic blood pressure from baseline to 3 months, measured in mmHg.ClinicalTrials.gov
SecondaryMean change in LDL cholesterol3 monthsChange in low-density lipoprotein (LDL) cholesterol level from baseline to 3 months, measured in mg/dL.ClinicalTrials.gov
SecondaryMean change in HDL cholesterol3 monthsChange in high-density lipoprotein (HDL) cholesterol level from baseline to 3 months, measured in mg/dL.ClinicalTrials.gov
SecondaryMean change in total cholesterol3 monthsChange in total cholesterol level from baseline to 3 months, measured in mg/dL.ClinicalTrials.gov
SecondaryMean change in HbA1c among participants with diabetes3 monthsChange in glycated hemoglobin (HbA1c) from baseline to 3 months among participants with diabetes, measured as a percentage (%).ClinicalTrials.gov
SecondarySystem Usability Scale (SUS) score3 monthsUsability of the web-based application will be assessed using the 10-item System Usability Scale (SUS), with total scores ranging from 0 to 100. Higher scores indicate better perceived usability.ClinicalTrials.gov
SecondaryChange in medication adherence score3 months
Change in medication adherence from baseline to 3 months, assessed using Adherence to Refills and Medications Scale (ARMS) questionnaire . It consists of 12 items covering two main domains: medication-taking behavior and prescription refill adherence Each item is scored on a 4-point Likert scale ranging from 1 (none of the time) to 4 (all of the time), with higher scores indicating lower adherence
ClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Grants 0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)