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| Name | Class |
|---|---|
| Population Council | OTHER |
| GRM Futures Group | UNKNOWN |
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This proposed study, to be run by Marie Stopes International Organisation Nigeria (MSION) will investigate whether Community Health Extension Workers (CHEWs) in Nigeria can insert and remove contraceptive implants to the same level of safety and quality as a nurse or midwife, and whether this is acceptable to their clients and colleagues. The study will also document feasibility issues which would be relevant to any future national programmatic scale-up.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Community health extension workers | Experimental | Community health extension workers providing contraceptive implants |
|
| Nurses and midwives | No Intervention | Nurses and midwives providing contraceptive implants (existing care) |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Training CHEWs to provide contraceptive implants | Other | Training CHEWs to provide contraceptive implants |
|
| Measure | Description | Time Frame |
|---|---|---|
| Adverse events | Any adverse event recorded by the health provider or the client on the day of the procedure | Day of implant insertion |
| Measure | Description | Time Frame |
|---|---|---|
| Quality of implant provision | Supervisor-recorded quality of service provision, which includes includes both clinical dimensions, such as cleanliness, and non-clinical dimensions, such as taking a client focused approach and being responsive to client needs | Day of implant insertion |
| Acceptability of service provision |
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Inclusion Criteria:
Exclusion Criteria:
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| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 29500162 | Derived | Reiss K, Penfold S, Alabi O, Ali M, Hopkins K, Ngo TD, Odogwu K, Douthwaite M, Ezire O, Udoh U, Effiom E, Munroe ES. Safety, Quality, and Acceptability of Contraceptive Subdermal Implant Provision by Community Health Extension Workers Versus Nurses and Midwives in Nigeria: Protocol for a Quasi-Experimental, Noninferiority Study. JMIR Res Protoc. 2018 Mar 2;7(3):e67. doi: 10.2196/resprot.8721. |
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Client-reported views of implant provision |
| Day of implant insertion |
| Adverse events | Any adverse event recorded by the health provider at the time of implant insertion or reported by the client on the day of the procedure or up to 14 days after the procedure | Up to 14 days post insertion |