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Lessons learnt from implementing an empirically informed recruitment approach for FEM-PrEP, a large HIV prevention clinical trial

Publication ,  Journal Article
Parker, C; Corneli, A; Agot, K; Odhiambo, J; Asewe, J; Ahmed, K; Skhosana, J; Ratlhagana, M; Lanham, M; Wong, C; Deese, J; Manongi, R ...
Published in: Open Access Journal of Clinical Trials
December 19, 2014

We implemented an empirically informed, geographically based recruitment approach for FEM-PrEP, a human immunodeficiency virus (HIV) prevention clinical trial of daily oral emtricitabine (FTC) and tenofovir disoproxil fumarate (TDF) for HIV prevention. During the formative research phase, we conducted a modification of the Priorities for Local AIDS Control Efforts (PLACE) method and used those data and staff experiences to identify and prioritize for recruitment geographic areas where HIV incidence might be high. During the clinical trial, we implemented a routinely monitored and flexible recruitment plan in the geographical areas identified in the formative research. We describe three lessons learnt from implementing this approach: 1) the PLACE data were critical in identifying places presumed to be high risk; 2) staff experiences, in combination with PLACE data, were needed to inform a practical recruitment strategy; and 3) recruiting in establishments in priority areas identified by the PLACE data led to screening many HIV-positive women at the Bondo site (Kenya), placing additional burden on clinic staff. These lessons learnt highlight the critical importance of having a flexible and monitored recruitment strategy. Although we successfully recruited a study population at higher risk for HIV, FEM-PrEP was unable to determine the effectiveness of FTC/TDF for HIV prevention, due to low adherence to the study product among participants. We must shift the paradigm of recruitment for clinical trials of new products from focusing on identifying populations with high incidence to identifying populations at risk who are motivated and able to adhere to the study product regimen.

Duke Scholars

Published In

Open Access Journal of Clinical Trials

DOI

EISSN

1179-1519

Publication Date

December 19, 2014

Volume

7

Start / End Page

1 / 9

Related Subject Headings

  • 3202 Clinical sciences
  • 1103 Clinical Sciences
 

Citation

APA
Chicago
ICMJE
MLA
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Parker, C., Corneli, A., Agot, K., Odhiambo, J., Asewe, J., Ahmed, K., … Malamatsho, R. (2014). Lessons learnt from implementing an empirically informed recruitment approach for FEM-PrEP, a large HIV prevention clinical trial. Open Access Journal of Clinical Trials, 7, 1–9. https://doi.org/10.2147/OAJCT.S68229
Parker, C., A. Corneli, K. Agot, J. Odhiambo, J. Asewe, K. Ahmed, J. Skhosana, et al. “Lessons learnt from implementing an empirically informed recruitment approach for FEM-PrEP, a large HIV prevention clinical trial.” Open Access Journal of Clinical Trials 7 (December 19, 2014): 1–9. https://doi.org/10.2147/OAJCT.S68229.
Parker C, Corneli A, Agot K, Odhiambo J, Asewe J, Ahmed K, et al. Lessons learnt from implementing an empirically informed recruitment approach for FEM-PrEP, a large HIV prevention clinical trial. Open Access Journal of Clinical Trials. 2014 Dec 19;7:1–9.
Parker, C., et al. “Lessons learnt from implementing an empirically informed recruitment approach for FEM-PrEP, a large HIV prevention clinical trial.” Open Access Journal of Clinical Trials, vol. 7, Dec. 2014, pp. 1–9. Scopus, doi:10.2147/OAJCT.S68229.
Parker C, Corneli A, Agot K, Odhiambo J, Asewe J, Ahmed K, Skhosana J, Ratlhagana M, Lanham M, Wong C, Deese J, Manongi R, Damme LV, Kiernan H, Mullins S, Omungo Z, Chett-Tyulsee S, Makatu S, Kapiga S, Malamatsho R. Lessons learnt from implementing an empirically informed recruitment approach for FEM-PrEP, a large HIV prevention clinical trial. Open Access Journal of Clinical Trials. 2014 Dec 19;7:1–9.

Published In

Open Access Journal of Clinical Trials

DOI

EISSN

1179-1519

Publication Date

December 19, 2014

Volume

7

Start / End Page

1 / 9

Related Subject Headings

  • 3202 Clinical sciences
  • 1103 Clinical Sciences