Oral Health
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ? Adult (18+ years, majority aged 30-50 years) ? Female or male ? Member of a household within the HDSS in Nouna. ? The medical history of the participant must be available. ? Has provided written informed consent to participate in the trial. ? Able and willing to consent for study participation
Exclusion criteria
Exclusion criteria: • Acute or chronic severe infections (diabetes mellitus, leukaemia, malnutrition, anticoagulant therapy) that prevent performing study activities. • Edentulism (person is missing all teeth) • Stomatitis • Silver allergy • Pregnant women • Women in their first 6 months of breastfeeding • Unable or unwilling to consent for study participation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Proportion of individuals with untreated active caries between study arms. | — |
Secondary
| Measure | Time frame |
|---|---|
| Prevalence of pain or infection among study participants.;Accuracy of oral screening by CHWs;Cost-effectiveness of the intervention. ;Safety of the intervention. ;Comparative evaluation of referrals from CHWs to the CSPSs and from there to the district hospital between intervention and control groups.;Precision of estimated ICC values based on collected data. | — |
Countries
Burkina Faso
Contacts
Section for Oral Health Heidelberg Institute of Global Health