Literature DB >> 20390489

Ensuring quality of services in HIV prevention research settings: findings from a multi-center quality improvement pilot in East Africa.

Prince Ngongo Bahati1, William Kidega, Hilda Ogutu, Jane Odada, Bonnie Bender, Pat Fast, Julie Becker, Matt Price.   

Abstract

Quality improvement (QI) has been widely implemented in health services but has not been widely applied in HIV prevention research. Most prevention research centers have commonly employed traditional approaches (e.g., checklists) to quality control that document what has been done but not the quality of what has been done. Unlike other health settings, prevention research settings have unique characteristics and ethical requirements that require the development or adaptation of specific quality indicators. A QI model for health services was adapted for use in prevention research settings and was piloted between August 2006 and July 2007 at three research centers in East Africa. Four hundred and twenty-six volunteers exit interviews were administered in two cycles. Quantitative and qualitative data were analyzed using Excel worksheets. QI meeting reports and QI plans were used to complement data from exit interviews. On average, 52% of total enrolled volunteers participated in the exit interview. The designed QI plans successfully helped reduce volunteers' reported waiting time to see counselors (p<0.001) and pharmacists (p<0.001). It also increased the percentage of interviewed volunteers who reported being counseled on family planning at clinical trials (from 66 to 93%; p=0.02) at follow-up visits, and who were refreshed on informed consent at follow-up visits (from 90 to 96%; p=0.009). The percentage of interviewed volunteers that expressed satisfaction with services received from counselors increased (from 87 to 94%; p=0.009) while the percentage of volunteer satisfied with services from trial physicians remained constant (93%). The majority of volunteers interviewed reported satisfaction with other major components of research such as confidentiality, understanding of trial objectives, benefits and risks of participation, and risk reduction counseling. However, satisfaction with services from community outreach workers and other staff at research centers dropped over the course of the study (from 88% in Cycle 1 to 74% in Cycle 3; p= < 0.001). Increased commitment to QI is crucial in ensuring quality of services and ethical conduct of HIV prevention research centers.

Mesh:

Year:  2010        PMID: 20390489     DOI: 10.1080/09540120903012569

Source DB:  PubMed          Journal:  AIDS Care        ISSN: 0954-0121


  3 in total

Review 1.  Trials need participants but not their feedback? A scoping review of published papers on the measurement of participant experience of taking part in clinical trials.

Authors:  Claire Planner; Peter Bower; Ailsa Donnelly; K Gillies; Katrina Turner; Bridget Young
Journal:  Trials       Date:  2019-06-24       Impact factor: 2.279

2.  Associations between mode of HIV testing and consent, confidentiality, and referral: a comparative analysis in four African countries.

Authors:  Carla Makhlouf Obermeyer; Melissa Neuman; Alice Desclaux; Rhoda Wanyenze; Odette Ky-Zerbo; Peter Cherutich; Ireen Namakhoma; Anita Hardon
Journal:  PLoS Med       Date:  2012-10-23       Impact factor: 11.069

3.  Motivations for entering and remaining in volunteer service: findings from a mixed-method survey among HIV caregivers in Zambia.

Authors:  Stephanie M Topp; Jessica E Price; Tina Nanyangwe-Moyo; Drosin M Mulenga; Mardieh L Dennis; Mathew M Ngunga
Journal:  Hum Resour Health       Date:  2015-09-02
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.