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NCT06845007Completed

PROMBot: A Web Platform for Collecting Outcomes for Hypertension Patients Via a Chatbot

PROMBot: A Web Platform for Collecting Patient-Reported Outcome Measures Via a Chatbot

Source: ClinicalTrials.gov · Last updated 13 Aug 2026

Brief summary (registry, in English)

The present study is observational and aims to evaluate the PROMBot service in managing patients' hypertension, simplify the follow-up process, and empower patients to actively participate in their own care.

Status (registry)
Completed
Study type
Observational
Enrollment
24 (actual)
First submitted
6 Feb 2025
Start date
6 Jan 2025
Primary completion date
1 Mar 2025
Lead sponsor
Ana Rita Londral
NCT number
NCT06845007

What you commit to

  • Study type: Observational
  • Participants enrolled: 24
  • From 6 Jan 2025 to the primary completion date, 1 Mar 2025
  • 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

  • Diagnosis of Parkinson's disease.
  • Diagnosis of cancer.

Other

  • Refusal to sign the informed consent form.
  • Mobility limitations that prevent engaging in physical activity.
  • Lack of a smartphone with internet access.

Who the study is looking for

  • Aged between 18 and 75 years old.
  • Diagnosed with hypertension, based on ICD-9 codes (401-401.9).
  • Independent in performing activities of daily living.
  • Ability to respond to SMS messages.

Age in the registry: 18 years to 75 years · Sex: All · Does not accept 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
CUF
Coordinator of this site? Confirm its status
LisbonPortugalUnknown status

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