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Bundling WhatsApp reminders with information targeting false beliefs to reduce missed follow-up visits for adults with hypertension: a randomized controlled trial in Punjab, India

Not Applicable
Recruiting
Conditions
I10
Essential (primary) hypertension
Registration Number
DRKS00029712
Lead Sponsor
Technical University of Munich
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
800
Inclusion Criteria

Participants need to be age > 18, have diagnosed or suspected hypertension as judged by their clinician, be able to speak and answer on their own, be able to read Punjabi, have their own phone with WhatsApp installed, have a clinician-requested follow-up visit for hypertension care that it at least 7 days after their initial visit, and consent to participate in our study.

Exclusion Criteria

Those who do not meet our inclusion criteria.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Whether trial participants came back for their follow-up appointment. We will assess this as a binary variable based on a patient visit database maintained by the study team.
Secondary Outcome Measures
NameTimeMethod
Our secondary outcome is participants' false beliefs about when to seek hypertension care. We will measure this through a phone-based questionnaire and analyze the outcomes as a continuous score based on the number of questions for which the participants gave an incorrect answer.
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