deltatrials
Completed NA INTERVENTIONAL 2-arm NCT02878200

RHOST-cRCT, Reactive Household-based Self-administered Treatment Against Residual Malaria Transmission (RHOST)

Reactive Household-based Self-administered Treatment Against Residual Malaria Transmission: a Cluster Randomized Trial

Sponsor: Institute of Tropical Medicine, Belgium

Conditions Malaria
Updated 11 times since 2017 Last updated: Sep 4, 2020 Started: Nov 4, 2016 Primary completion: Dec 18, 2018 Completion: Jul 16, 2020
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

This NA trial investigates Malaria and is currently completed. Institute of Tropical Medicine, Belgium leads this study, which shows 11 recorded versions since 2016 — indicating substantial longitudinal coverage. Longitudinal tracking of infectious disease trials helps identify durability of treatment effects.

Study Description(click to expand)

Achieving malaria elimination presents a challenge because of important gaps in the knowledge about the strategies and tools needed achieve this. While malaria control measures aim to reduce morbidity and mortality in vulnerable populations, interventions to reduce transmission are designed to interrupt transmission of malaria parasites from humans, especially asymptomatic parasite carriers \[1\], to mosquitoes. The importance of asymptomatic infections in transmission has grown with the awareness that the majority of the human reservoir of infection are asymptomatic carriers \[2\] and these are quite difficult to target \[3\]. Previous malaria elimination campaigns have applied a strategy of mass drug administration: extensive treatment of entire populations, irrespective of their infection status, in one or multiple rounds \[4\]. Although transmission was interrupted in some cases, albeit temporarily \[5\], there is a reluctance to apply this method because the evidence of its impact has been mixed. A Cochrane systematic review of MDAs showed that long term reductions were not possible within the current concept and highlighted the need for studies in low- and moderate-transmission settings and studies that could address potential barriers for community uptake, and contribution to the development of drug resistance \[6\]. More conservative approaches involving screening for infection with a...

Achieving malaria elimination presents a challenge because of important gaps in the knowledge about the strategies and tools needed achieve this. While malaria control measures aim to reduce morbidity and mortality in vulnerable populations, interventions to reduce transmission are designed to interrupt transmission of malaria parasites from humans, especially asymptomatic parasite carriers \[1\], to mosquitoes.

The importance of asymptomatic infections in transmission has grown with the awareness that the majority of the human reservoir of infection are asymptomatic carriers \[2\] and these are quite difficult to target \[3\]. Previous malaria elimination campaigns have applied a strategy of mass drug administration: extensive treatment of entire populations, irrespective of their infection status, in one or multiple rounds \[4\]. Although transmission was interrupted in some cases, albeit temporarily \[5\], there is a reluctance to apply this method because the evidence of its impact has been mixed. A Cochrane systematic review of MDAs showed that long term reductions were not possible within the current concept and highlighted the need for studies in low- and moderate-transmission settings and studies that could address potential barriers for community uptake, and contribution to the development of drug resistance \[6\].

More conservative approaches involving screening for infection with a rapid malaria diagnostic test (RDT) and treating only positive individuals; mass screening and treatment, did not have a significant impact on the malaria incidence \[7\], largely due to low test's sensitivity that would miss a large proportion of infected individuals with low parasite densities. Implementing reactive screening on a programmatic scale puts significant pressure on the health system \[8\] and available field-based screening tests lack the required sensitivity for low-density parasitaemia seen with asymptomatic infections \[9\]. More importantly, understanding the local context and adapting intervention strategies may help improve coverage and participation by recipient communities \[10\].

This study investigates a novel approach to reducing residual malaria transmission that combines the elements of reactive treatment of household contacts of a clinical case reporting at a health facility with the active involvement of both patients and their households. The approach to implementation will be developed through formative research that identifies the optimum means of community engagement that will result in the best possible compliance and adherence to the treatment in the household.

Status Flow

~Jan 2017 – ~Apr 2018 · 15 months · monthly snapshotRecruiting~Apr 2018 – ~Jun 2018 · 2 months · monthly snapshotRecruiting~Jun 2018 – ~Dec 2018 · 6 months · monthly snapshotRecruiting~Dec 2018 – ~Feb 2019 · 2 months · monthly snapshotRecruiting~Feb 2019 – ~Jun 2019 · 4 months · monthly snapshotRecruiting~Jun 2019 – ~Oct 2020 · 16 months · monthly snapshotActive Not Recruiting~Oct 2020 – ~Jan 2021 · 3 months · monthly snapshotCompleted~Jan 2021 – ~Jul 2024 · 42 months · monthly snapshotCompleted~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshotCompleted~Sep 2024 – ~Sep 2025 · 12 months · monthly snapshotCompleted~Sep 2025 – present · 7 months · monthly snapshotCompleted

Change History

11 versions recorded
  1. Sep 2025 — Present [monthly]

    Completed NA

  2. Sep 2024 — Sep 2025 [monthly]

    Completed NA

  3. Jul 2024 — Sep 2024 [monthly]

    Completed NA

  4. Jan 2021 — Jul 2024 [monthly]

    Completed NA

  5. Oct 2020 — Jan 2021 [monthly]

    Completed NA

    Status: Active Not RecruitingCompleted

Show 6 earlier versions
  1. Jun 2019 — Oct 2020 [monthly]

    Active Not Recruiting NA

    Status: RecruitingActive Not Recruiting

  2. Feb 2019 — Jun 2019 [monthly]

    Recruiting NA

  3. Dec 2018 — Feb 2019 [monthly]

    Recruiting NA

  4. Jun 2018 — Dec 2018 [monthly]

    Recruiting NA

  5. Apr 2018 — Jun 2018 [monthly]

    Recruiting NA

  6. Jan 2017 — Apr 2018 [monthly]

    Recruiting NA

    First recorded

Nov 2016

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Institute of Tropical Medicine, Belgium
  • London School of Hygiene and Tropical Medicine
  • University of Sheffield
Data source: London School of Hygiene and Tropical Medicine

For direct contact, visit the study record on ClinicalTrials.gov .