TY - JOUR
T1 - Slash and clear' vector control for onchocerciasis elimination and epilepsy prevention
T2 - A protocol of a cluster randomised trial in Cameroonian villages
AU - Siewe Fodjo, Joseph Nelson
AU - Vieri, Melissa Krizia
AU - Ngarka, Leonard
AU - Njamnshi, Wepnyu Y.
AU - Nfor, Leonard N.
AU - Mengnjo, Michel Karngong
AU - Hendy, Adam
AU - Enyong, Peter A.
AU - Palmer, Dennis
AU - Basanez, Maria Gloria
AU - Colebunders, Robert
AU - Njamnshi, Alfred K.
N1 - Funding Information:
Funding This project is part of the second European and Developing Countries Clinical Trials Partnership (EDCTP2) programme supported by the European Union (grant number: TMA2020CDF-3152-SCONE), with additional funding obtained via the Royal Society of Tropical Medicine and Hygiene (2020 small grants session), both awarded to JNSF. MGB acknowledges joint centre funding (grant number: MR/ R015600/1) by the UK Medical Research Council (MRC) and the UK Department for International Development (DFID) under the MRC/DFID concordat agreement, which is also a part of the EDCTP2 programme supported by the European Union. The sponsors had no role in the design and decision to publish this protocol.
Publisher Copyright:
© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
PY - 2021/9/2
Y1 - 2021/9/2
N2 - Introduction Onchocerciasis, caused by the filarial nematode Onchocerca volvulus, remains endemic in Cameroon despite decades of community-directed treatment with ivermectin (CDTI). CDTI is often hampered by coendemicity with loiasis (another filariasis caused by Loa loa) in some areas. Strong epidemiological evidence suggests that O. volvulus infection increases the risk for onchocerciasis-Associated epilepsy (OAE) among Cameroonian children. This highlights the urgent need to strengthen onchocerciasis elimination programmes in mesoendemic/hyperendemic areas. Novel alternative strategies, such as the â € slash and clear' (SC) vector control method, may be required to complement ongoing CDTI to accelerate elimination of transmission. The short-Term impact of SC on the biting rates of the blackfly vectors has been demonstrated in other settings. However, its long-Term effectiveness and impact on parasitological and serological markers of onchocerciasis transmission as well as on OAE are still unknown. Methods and analysis We aim to assess the effectiveness of annual SC interventions combined with CDTI in reducing onchocerciasis transmission and epilepsy incidence. Eight onchocerciasis-endemic villages located <5 km from the Mbam or Sanaga rivers will be randomised to two arms: four villages will receive yearly CDTI only for two consecutive years (Arm 1), while the other four villages will receive CDTI plus annual SC for 2 years (Arm 2). Study outcomes (blackfly biting rates, infectivity rates and seroprevalence of onchocerciasis antibodies (Ov16 antibodies) in children, prevalence of microfilaridermia and epilepsy incidence) will be monitored prospectively and compared across study arms. We expect that SC will have an added benefit over CDTI alone. Ethics and dissemination The protocol has received ethical approval from the institutional review board of the Cameroon Baptist Convention Health Board (reference number: IRB2021-03) and has been registered with the Pan African Clinical Trials Registry. Findings will be disseminated at national and international levels via meetings and peer-reviewed publications. Trial registration number PACTR202101751275357.
AB - Introduction Onchocerciasis, caused by the filarial nematode Onchocerca volvulus, remains endemic in Cameroon despite decades of community-directed treatment with ivermectin (CDTI). CDTI is often hampered by coendemicity with loiasis (another filariasis caused by Loa loa) in some areas. Strong epidemiological evidence suggests that O. volvulus infection increases the risk for onchocerciasis-Associated epilepsy (OAE) among Cameroonian children. This highlights the urgent need to strengthen onchocerciasis elimination programmes in mesoendemic/hyperendemic areas. Novel alternative strategies, such as the â € slash and clear' (SC) vector control method, may be required to complement ongoing CDTI to accelerate elimination of transmission. The short-Term impact of SC on the biting rates of the blackfly vectors has been demonstrated in other settings. However, its long-Term effectiveness and impact on parasitological and serological markers of onchocerciasis transmission as well as on OAE are still unknown. Methods and analysis We aim to assess the effectiveness of annual SC interventions combined with CDTI in reducing onchocerciasis transmission and epilepsy incidence. Eight onchocerciasis-endemic villages located <5 km from the Mbam or Sanaga rivers will be randomised to two arms: four villages will receive yearly CDTI only for two consecutive years (Arm 1), while the other four villages will receive CDTI plus annual SC for 2 years (Arm 2). Study outcomes (blackfly biting rates, infectivity rates and seroprevalence of onchocerciasis antibodies (Ov16 antibodies) in children, prevalence of microfilaridermia and epilepsy incidence) will be monitored prospectively and compared across study arms. We expect that SC will have an added benefit over CDTI alone. Ethics and dissemination The protocol has received ethical approval from the institutional review board of the Cameroon Baptist Convention Health Board (reference number: IRB2021-03) and has been registered with the Pan African Clinical Trials Registry. Findings will be disseminated at national and international levels via meetings and peer-reviewed publications. Trial registration number PACTR202101751275357.
KW - entomology
KW - epilepsy
KW - parasitology
KW - preventive medicine
KW - public health
UR - http://www.scopus.com/inward/record.url?scp=85114467646&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85114467646&partnerID=8YFLogxK
U2 - 10.1136/bmjopen-2021-050341
DO - 10.1136/bmjopen-2021-050341
M3 - Article
C2 - 34475178
AN - SCOPUS:85114467646
SN - 2044-6055
VL - 11
JO - BMJ open
JF - BMJ open
IS - 9
M1 - e050341
ER -