Efficacy of the Artificial Intelligence HeartBot II in Increasing Awareness and Knowledge of Heart Attack in Women: Study Protocol for a Randomized Controlled Trial With a Waitlist Control

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Record identity and dates

Source

ClinicalTrials.gov

Source record ID

NCT07416734

Title field or adapter rule

protocolSection.identificationModule.officialTitle

Ingested At

2026-04-25T22:28:24.756379+00:00

Published At

2026-02-18T00:00:00+00:00

Record Updated At

2026-02-18

Timestamp Basis

source retrieval time was not retained by the feed adapter

Date limitation

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Fields recorded by this source

protocolSection.conditionsModule.conditions

["Participants Must be Women Aged 25 Years or Older", "Participants Should Have no Self-reported History of Heart Disease or Stroke", "Participants Should Have no Terminal Illness or Diagnosed Cognitive Impairment, Including Alzheimer\u0027s Disease", "Participants Should Not be a Healthcare Professionals or Healthcare Trainees", "Participants Should Not be Employed in the Healthcare Field", "Participants Should Reside in the United States and be a University of California, San Francisco Health Patient", "Participants Should Possess a Smartphone With an Active Data Plan or Access to Wi-Fi"]

protocolSection.statusModule.lastUpdatePostDateStruct.date

"2026-02-18"

protocolSection.identificationModule.nctId

"NCT07416734"

protocolSection.identificationModule.officialTitle

"Efficacy of the Artificial Intelligence HeartBot II in Increasing Awareness and Knowledge of Heart Attack in Women: Study Protocol for a Randomized Controlled Trial With a Waitlist Control"

protocolSection.statusModule.overallStatus

"NOT_YET_RECRUITING"

protocolSection.designModule.phases

["NA"]

protocolSection.statusModule.resultsFirstPostDateStruct.date

""

Study condition terms

• Participants Must be Women Aged 25 Years or Older (protocolSection.conditionsModule.conditions)
• Participants Should Have no Self-reported History of Heart Disease or Stroke (protocolSection.conditionsModule.conditions)
• Participants Should Have no Terminal Illness or Diagnosed Cognitive Impairment, Including Alzheimer's Disease (protocolSection.conditionsModule.conditions)
• Participants Should Not be a Healthcare Professionals or Healthcare Trainees (protocolSection.conditionsModule.conditions)
• Participants Should Not be Employed in the Healthcare Field (protocolSection.conditionsModule.conditions)
• Participants Should Reside in the United States and be a University of California, San Francisco Health Patient (protocolSection.conditionsModule.conditions)
• Participants Should Possess a Smartphone With an Active Data Plan or Access to Wi-Fi (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

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