Plasmodium vivax
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Aged 16 years or older at the time of enrollment; Laboratory-confirmed diagnosis of uncomplicated Plasmodium vivax malaria; Prescribed a chloroquine and primaquine daily treatment regimen according to national guidelines; Access to a personal mobile phone capable of receiving SMS or WhatsApp messages; Provided written informed consent before study participation
Exclusion criteria
Exclusion criteria: Diagnosis of severe malaria or infection with non-P. vivax species; Inability to provide informed consent due to severe cognitive impairment; No access to a mobile phone capable of receiving SMS or WhatsApp messages; Known contraindications or allergies to chloroquine or primaquine; Residence outside the study's catchment area where follow-up is not feasible
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to observe treatment adherence between days 7 and 12 after treatment initiation, determined by the 4-item Morisky Medication Adherence Scale (MMAS-4) | — |
Secondary
| Measure | Time frame |
|---|---|
| It has no secondary outcome | — |
Countries
Brazil
Contacts
Fundacão de Medicina Tropical Heitor Vieira Dourado