PROMBot: a Web Platform for Collecting Patient-Reported Outcome Measures Via a Chatbot
Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY
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.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:
• 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.
Locations
Other Locations
Portugal
CUF
RECRUITING
Lisbon
Contact Information
Primary
Soraia Ferreira, PhD
soraia.ferreira@vohcolab.org
969307101
Time Frame
Start Date: 2025-01-06
Estimated Completion Date: 2025-06
Participants
Target number of participants: 30
Treatments
Hypertension Group
This study includes only one group. This group will consist of patients with hypertension, and after a patient is identified, they will be followed up using the PROMBot platform for the subsequent 12 weeks. In the first week, the patient will be required to record their diastolic and systolic blood pressure values daily and answer a quiz on hypertension-related topics. In the second week, the participant will continue recording their blood pressure values, but only every other day. From the third to the tenth week, the participant may choose to receive tips on nutrition recipes and exercises they can perform to increase physical activity. In the 11th week, the participant will again measure their blood pressure, but the values will only be recorded on the 1st, 3rd, 5th, and 7th days. Finally, in the 12th week, the participant will resume recording daily blood pressure values in PROMBot.
Related Therapeutic Areas
Sponsors
Leads: Ana Rita Londral