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  <eprint id='https://datacompass.lshtm.ac.uk/id/eprint/5160'>
    <eprintid>5160</eprintid>
    <rev_number>5</rev_number>
    <eprint_status>archive</eprint_status>
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    <dir>disk0/00/00/51/60</dir>
    <datestamp>2026-04-22 10:14:36</datestamp>
    <lastmod>2026-04-22 10:14:36</lastmod>
    <status_changed>2026-04-22 10:14:36</status_changed>
    <type>data_collection</type>
    <metadata_visibility>show</metadata_visibility>
    <item_issues_count>1</item_issues_count>
    <creators>
      <item>
        <name>
          <family>Bousema</family>
          <given>Teun</given>
        </name>
        <lshtm_flag>TRUE</lshtm_flag>
        <staffid>7f95d700c86761c95206dd30215ad788</staffid>
      </item>
      <item>
        <name>
          <family>Drakeley</family>
          <given>Chris</given>
        </name>
        <orcid>0000-0003-4863-075X</orcid>
        <lshtm_flag>TRUE</lshtm_flag>
        <staffid>3fdd056af9618ed15655a13cb59c4d2e</staffid>
      </item>
      <item>
        <name>
          <family>Tiono</family>
          <given>Alfred</given>
        </name>
        <lshtm_flag>TRUE</lshtm_flag>
        <staffid>5bb63b4c3b8b97c4afe89633516372bc</staffid>
      </item>
    </creators>
    <corp_creators>
      <item>London School of Hygiene &amp; Tropical Medicine, London, United Kingdom</item>
    </corp_creators>
    <title>Data from: Impact of directly observed treatment and extended age-range of seasonal malaria chemoprevention with sulfadoxine–pyrimethamine plus amodiaquine in Burkina Faso: A three-arm, open-label, cluster-randomized, controlled trial</title>
    <divisions>
      <item>ITIB</item>
    </divisions>
    <keywords>
      <item>Chemoprevention</item>
      <item>Clinical trials</item>
      <item>Cluster trials</item>
      <item>Malaria</item>
      <item>Medical and health sciences</item>
    </keywords>
    <abstract>Seasonal Malaria Chemoprevention (SMC) currently targets children below 5 years (&lt; 5 yr). It is unclear what the impact of extending SMC to a wider age range will be. We conducted a cluster-randomized trial in Saponé (Burkina Faso) with three study arms: 1) Programmatic SMC-control arm: SMC in children &lt; 5 years; 2) SMC in children &lt; 5 years, with directly observed treatment (DOTu5); 3) SMC in children &lt; 10 years with DOT (DOTu10). The trial involved 61 (programmatic SMC) and 62 (each DOT arms) clusters of 3 compounds (i.e., 183-186 compounds per arm). The primary endpoint was P. falciparum parasite prevalence at the end of the transmission season; secondary endpoints included clinical malaria incidence, drug plasma levels, and gametocyte prevalence. This trial is complete and is registered with ClinicalTrials.gov, NCT05878366.</abstract>
    <date>2026-03-19</date>
    <date_type>published</date_type>
    <publisher>Dryad</publisher>
    <data_type>Dataset</data_type>
    <copyright_holders>
      <item>Study authors</item>
    </copyright_holders>
    <collection_mode>
      <item>SelfAdministeredQuestionnaire</item>
      <item>MeasurementsAndTests</item>
    </collection_mode>
    <full_text_status>none</full_text_status>
    <resourcetype>
      <resourcetypegeneral>Dataset</resourcetypegeneral>
      <resourcetype>Quantitative</resourcetype>
    </resourcetype>
    <language>
      <item>en</item>
    </language>
    <related_resources>
      <item>
        <title>Dryad Digital Repository</title>
        <url>https://doi.org/10.5061/dryad.9cnp5hr0p</url>
        <type>dataresource</type>
      </item>
    </related_resources>
    <repo_link>
      <item>
        <title>Understanding and maximising the community impact of seasonal malaria chemoprevention in Burkina Faso (INDIE-SMC): study protocol for a cluster randomised evaluation trial.</title>
        <link>https://researchonline.lshtm.ac.uk/id/eprint/4673785</link>
      </item>
    </repo_link>
    <ukri_date_sub>2026-03-19</ukri_date_sub>
  </eprint>
</eprints>
