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Pragmatism in practice: lessons learned during screening and enrollment for a randomised controlled trial in rural northern Ethiopia.
Molla, Meseret; Negussie, Henok; Ngari, Moses; Kivaya, Esther; Njuguna, Patricia; Enqueselassie, Fikre; Berkley, James A; Davey, Gail.
  • Molla M; Centre for Environment and Development Studies, Addis Ababa University, Addis Ababa, Ethiopia.
  • Negussie H; Wellcome Trust Centre for Global Health Research, Brighton & Sussex Medical School, University of Sussex, Brighton, BN1 9PX, UK.
  • Ngari M; KEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.
  • Kivaya E; KEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.
  • Njuguna P; KEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.
  • Enqueselassie F; School of Public Health, Addis Ababa University, Addis Ababa, Ethiopia.
  • Berkley JA; KEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.
  • Davey G; Centre for Tropical Medicine & Global Health, University of Oxford, Oxford, UK.
BMC Med Res Methodol ; 18(1): 26, 2018 03 07.
Article en En | MEDLINE | ID: mdl-29514613
ABSTRACT

BACKGROUND:

We use the example of the Gojjam Lymphoedema Best Practice Trial (GoLBeT), a pragmatic trial in a remote rural setting in northern Ethiopia, to extract lessons relevant to other investigators balancing the demands of practicality and community acceptability with internal and external validity in clinical trials.

METHODS:

We explain in detail the preparation for the trial, its setting in northern Ethiopia, the identification and selection of patients (inclusion and exclusion criterion, identifying and screening of patients at home, enrollment of patients at the health centres and health posts), and randomisation.

RESULTS:

We describe the challenges met, together with strategies employed to overcome them.

CONCLUSIONS:

Examples given in the previous section are contextualised and general principles extracted where possible. We conclude that it is possible to conduct a trial that balances approaches that support internal validity (e.g. careful design of proformas, accurate case identification, control over data quality and high retention rates) with those that favour generalisability (e.g. 'real world' setting and low rates of exclusion). Strategies, such as Rapid Ethical Assessment, that increase researchers' understanding of the study setting and inclusion of hard-to-reach participants are likely to have resource and time implications, but are vital in achieving an appropriate balance. TRIAL REGISTRATION ISRCTN67805210, registered 24/01/2013.
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Texto completo: 1 Ejes tematicos: Pesquisa_clinica Banco de datos: MEDLINE Asunto principal: Ensayos Clínicos Controlados Aleatorios como Asunto / Tamizaje Masivo / Ensayos Clínicos Pragmáticos como Asunto / Linfedema Tipo de estudio: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Límite: Humans País como asunto: Africa Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Ejes tematicos: Pesquisa_clinica Banco de datos: MEDLINE Asunto principal: Ensayos Clínicos Controlados Aleatorios como Asunto / Tamizaje Masivo / Ensayos Clínicos Pragmáticos como Asunto / Linfedema Tipo de estudio: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Límite: Humans País como asunto: Africa Idioma: En Año: 2018 Tipo del documento: Article