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Preserving ACTs - Text Reminders to Increase Adherence to ACT Treatment

Not Applicable
Completed
Conditions
Malaria
Interventions
Behavioral: Text message reminders
Registration Number
NCT01722734
Lead Sponsor
Harvard School of Public Health (HSPH)
Brief Summary

A randomized controlled trial was conducted to assess the effectiveness of text reminders sent to ACT users through an automated text messaging system short-message-system.

Study hypothesis: text message reminders increase adherence

Detailed Description

A randomized controlled trial was conducted to assess the effectiveness of text reminders sent to ACT users through an automated text messaging system short-message-system. Patients were enrolled at clinics and pharmacies upon receipt of ACTs and enrolled in the automated system for 3 days.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1140
Inclusion Criteria

-subjects acquiring ACTs in Tamale, Ghana

Exclusion Criteria
  • subjects acquiring ACTs for non household members
  • subjects under the age of 18
  • subjects without access to cell phones
  • subjects living more than 30 minutes from pickup location

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Short MessageText message remindersPatients in this arm receive six short text message reminders within 60 hours of treatment initiation at 12 hour intervals.
Long messageText message remindersPatients in this arm receive six long text message reminders (reminders including justification for why patients should finish medication) within 60 hours of treatment initiation at 12 hour intervals.
Primary Outcome Measures
NameTimeMethod
Self-reported Adherence to Artemisinin-combination Therapy (ACT) Treatment70 hours

Percentage of participants completing full ACT treatment regimen 70 hours after treatment initiation. Subjects were visited at home, and asked to report when each of the prescribed six doses were taken. Adherence was defined as the (self-reported) completion of all six doses.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Study site

🇬🇭

Tamale, Northern Region, Ghana

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