<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Matoga MM</submitter><funding>FIC NIH HHS</funding><funding>NIH</funding><pagination>e072855</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10552000</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(10)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>To evaluate the effect a multistrategy demand-creation and linkage intervention on voluntary medical male circumcision (VMMC) uptake, time to VMMC and predictors of VMMC uptake among men with sexually transmitted infections (STIs).&lt;h4>Design&lt;/h4>Pragmatic preinterventional and postinterventional quasi-experimental study combined with a prospective observational design.&lt;h4>Setting&lt;/h4>A public and specialised STI clinic in Lilongwe, Malawi.&lt;h4>Population&lt;/h4>Uncircumcised men who presented to the STI clinic.&lt;h4>Methods and intervention&lt;/h4>The intervention consisted of transport reimbursement ('R'), intensified health education ('I') and short-messaging services/telephonic tracing ('Te'), abbreviated (RITe). A preintervention phase was conducted at baseline while RITe was rolled-out in the intervention phase in a sequential manner called implementation blocks: 'I' only-block 1; 'I+Te'-block 2 and RITe-block 3.&lt;h4>Main outcome measures&lt;/h4>Primary: VMMC uptake and time to VMMC for the full intervention and for each block. Secondary: predictors of VMMC uptake.&lt;h4>Results&lt;/h4>A total of 2230 uncircumcised men presented to the STI clinic. The mean age was 29 years (SD±9), 58% were married/cohabiting, HIV prevalence was 6.4% and 43% had urethral discharge. Compared with standard of care (8/514, 1.6%), uptake increased by 100% during the intervention period (55/1716, 3.2%) (p=0.048). 'I' (25/731, 113%, p=0.044) and RITe (17/477, 125%, p=0.044) significantly increased VMMC uptake. The median time to VMMC was shorter during the intervention period (6 days, IQR: 0, 13) compared with standard of care (15 days, IQR: 9, 18). There was no significant incremental effect on VMMC uptake and time to VMMC between blocks. Men with genital warts were 18 times more likely to receive VMMC (adjusted relative risk=18.74, 95% CI: 2.041 to 172.453).&lt;h4>Conclusions&lt;/h4>Our intervention addressing barriers to VMMC improved VMMC uptake and time to VMMC among uncircumcised men with STIs, an important subpopulation for VMMC prioritisation.&lt;h4>Trial registration number&lt;/h4>NCT04677374.</pubmed_abstract><journal>BMJ open</journal><pubmed_title>Effectiveness of an intervention to increase uptake of voluntary medical male circumcision among men with sexually transmitted infections in Malawi: a preinterventional and postinterventional study.</pubmed_title><pmcid>PMC10552000</pmcid><funding_grant_id>D43 TW009774-06</funding_grant_id><funding_grant_id>D43 TW009774</funding_grant_id><funding_grant_id>D43 TW009340</funding_grant_id><funding_grant_id>D43 TW010060</funding_grant_id><pubmed_authors>Chagomerana M</pubmed_authors><pubmed_authors>Ndalama B</pubmed_authors><pubmed_authors>Kamtambe B</pubmed_authors><pubmed_authors>Jere E</pubmed_authors><pubmed_authors>Chasela C</pubmed_authors><pubmed_authors>Matoga MM</pubmed_authors><pubmed_authors>Bonongwe N</pubmed_authors><pubmed_authors>Hosseinipour MC</pubmed_authors><pubmed_authors>Mathiya E</pubmed_authors><pubmed_authors>Kudowa E</pubmed_authors><pubmed_authors>Jewett S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effectiveness of an intervention to increase uptake of voluntary medical male circumcision among men with sexually transmitted infections in Malawi: a preinterventional and postinterventional study.</name><description>&lt;h4>Objective&lt;/h4>To evaluate the effect a multistrategy demand-creation and linkage intervention on voluntary medical male circumcision (VMMC) uptake, time to VMMC and predictors of VMMC uptake among men with sexually transmitted infections (STIs).&lt;h4>Design&lt;/h4>Pragmatic preinterventional and postinterventional quasi-experimental study combined with a prospective observational design.&lt;h4>Setting&lt;/h4>A public and specialised STI clinic in Lilongwe, Malawi.&lt;h4>Population&lt;/h4>Uncircumcised men who presented to the STI clinic.&lt;h4>Methods and intervention&lt;/h4>The intervention consisted of transport reimbursement ('R'), intensified health education ('I') and short-messaging services/telephonic tracing ('Te'), abbreviated (RITe). A preintervention phase was conducted at baseline while RITe was rolled-out in the intervention phase in a sequential manner called implementation blocks: 'I' only-block 1; 'I+Te'-block 2 and RITe-block 3.&lt;h4>Main outcome measures&lt;/h4>Primary: VMMC uptake and time to VMMC for the full intervention and for each block. Secondary: predictors of VMMC uptake.&lt;h4>Results&lt;/h4>A total of 2230 uncircumcised men presented to the STI clinic. The mean age was 29 years (SD±9), 58% were married/cohabiting, HIV prevalence was 6.4% and 43% had urethral discharge. Compared with standard of care (8/514, 1.6%), uptake increased by 100% during the intervention period (55/1716, 3.2%) (p=0.048). 'I' (25/731, 113%, p=0.044) and RITe (17/477, 125%, p=0.044) significantly increased VMMC uptake. The median time to VMMC was shorter during the intervention period (6 days, IQR: 0, 13) compared with standard of care (15 days, IQR: 9, 18). There was no significant incremental effect on VMMC uptake and time to VMMC between blocks. Men with genital warts were 18 times more likely to receive VMMC (adjusted relative risk=18.74, 95% CI: 2.041 to 172.453).&lt;h4>Conclusions&lt;/h4>Our intervention addressing barriers to VMMC improved VMMC uptake and time to VMMC among uncircumcised men with STIs, an important subpopulation for VMMC prioritisation.&lt;h4>Trial registration number&lt;/h4>NCT04677374.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Oct</publication><modification>2026-03-31T11:39:26.382Z</modification><creation>2025-04-19T07:16:42.87Z</creation></dates><accession>S-EPMC10552000</accession><cross_references><pubmed>37788927</pubmed><doi>10.1136/bmjopen-2023-072855</doi></cross_references></HashMap>