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NCT07416734Not yet recruiting

RCT of HeartBot in Women

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

Source: ClinicalTrials.gov · Last updated 18 Feb 2026

Brief summary (registry, in English)

The goal of this clinical trial is to find out whether an app-based program called HeartBot II, which uses an artificial intelligence (AI) chatbot, can help improve women's awareness and knowledge of heart attacks in women. This is an online study with about 200 women taking part. Participants will be randomly assigned (by chance) to one of two groups: an intervention group or a wait-list control group. Participants in the intervention group will begin using the HeartBot II program right away. Participants in the wait-list control group will wait 12 weeks before starting the HeartBot II program. The HeartBot II program includes four short modules. In each module, participants will interact with a chatbot and spend about 10 to 15 minutes completing the content. Participants will be asked to complete an online screening and baseline survey at the start of the study, as well as two follow-up surveys at 12 weeks and 24 weeks.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
200 (estimated)
First submitted
11 Feb 2026
Start date
1 Mar 2026
Primary completion date
30 Jun 2027
Lead sponsor
University of California, San Francisco
NCT number
NCT07416734

What you commit to

  • Study type: Interventional
  • Planned participants: 200
  • From 1 Mar 2026 to the primary completion date, 30 Jun 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Having self-reported cognitive impairment
  • Having history of heart disease or stroke

Other

  • Individuals who identify as male
  • Healthcare professional/trainee
  • Working in the healthcare field

Who the study is looking for

  • Women
  • 25 years or older
  • Living in the US
  • University of California, San Francisco Health patient
  • Possessing a smartphone with a data plan or Wi-Fi access

Age in the registry: 25 years to - · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of California San Francisco
Coordinator of this site? Confirm its status
San FranciscoUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.