Cargando…

Factors affecting the understanding and retention of the informed consent among participants at an antiretroviral clinical trial in a resource limited setting

Detalles Bibliográficos
Autor principal:	Salami, Donald
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2013
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981049/ http://dx.doi.org/10.1186/1745-6215-14-S1-P89

Ejemplares similares

Can we improve recruitment to trials and informed consent by improving participant information sheets? - A nested RCT
por: Knapp, Peter, et al.
Publicado: (2011)

Electronic informed consent
por: Stevens, Natasha
Publicado: (2013)

“To have, to hold, from this day forward”: understanding current practice regarding the retention of trial participants
por: Daykin, Anne, et al.
Publicado: (2015)

Evaluation of interventions for informed consent for randomised controlled trials (ELICIT): developing a core outcome set
por: Gillies, Katie, et al.
Publicado: (2015)

Knowledge of confidentiality, consent and information disclosure is not affected by position or experience in adult critical care
por: Lowings, M, et al.
Publicado: (2013)

EvaLuation of Interventions for informed Consent for randomIsed controlled Trials (ELICIT): developing a core outcome set
por: Gillies, Katie, et al.
Publicado: (2015)

Practice of the principle of right conduct in obtaining informed consents and legibility of the consent forms - a clinical audit
por: Hassan, R, et al.
Publicado: (2015)

Device for measuring bronchodilator delivery and response in resource-limited settings
por: Carspecken, CW, et al.
Publicado: (2013)

Exploring research participants’ perceptions and comprehension of the informed consent process in a pre-exposure HIV prevention study: a case study
por: Ruzario, S, et al.
Publicado: (2012)

P15-16. Social factors affecting retention rates in Step study participants in Lima-Peru
por: Fernandez-Maldonado, MD, et al.
Publicado: (2009)

The trialists’ perspectives on the participant retention in mental health randomised controlled trials
por: Szymczynska, Paulina, et al.
Publicado: (2015)

Analysis of patient information leaflets (PILs), used in clinical trials using the Informed Consent Evaluation instrument (ICEi)
por: Gillies, Katie, et al.
Publicado: (2011)

Feasibility of routine data collection on icu performance and activity in resource limited settings
por: Ali, SMM, et al.
Publicado: (2015)

Evaluation of the AIDS clinical trials group staging criteria for Kaposi Sarcoma in a resource limited setting
por: Okuku, Fred, et al.
Publicado: (2012)

Developing easy access patient information booklets and consent forms for use in multicentre stroke trials
por: Mead, Gillian, et al.
Publicado: (2013)

Assessing the quality of informed consent in a resource-limited setting: A cross-sectional study
por: Kiguba, Ronald, et al.
Publicado: (2012)

Evaluating informed consent during trial recruitment consultations: development and preliminary evaluation of a new method
por: Wade, Julia, et al.
Publicado: (2015)

P14-05. Recruitment, retention and participation impact events among women participating in phase III community trial in Thailand
por: Pitisuttithum, P, et al.
Publicado: (2009)

Understanding and retention of the informed consent process among parents in rural northern Ghana
por: Oduro, Abraham R, et al.
Publicado: (2008)

Development of a severe influenza critical care curriculum and training materials for resource-limited settings
por: Diaz, JV, et al.
Publicado: (2013)

Health literacy predicts participant understanding of orally-presented informed consent information
por: Ownby, Raymond L, et al.
Publicado: (2015)

Antiretroviral Treatment in Resource-Limited Settings 2012
por: Duerr, Ann, et al.
Publicado: (2012)

P64 Improving surgical consent – a quality improvement project to enhance the consenting process
por: Shrivastava, Manu, et al.
Publicado: (2021)

A survey of study participants’ understanding of informed consent to participate in a randomised controlled trial of acupuncture
por: Smith, Caroline A., et al.
Publicado: (2016)

P103 Research governance audit on quality of documentation of hyperacute ATTEST 2 stroke trial, focusing on the informed consent process
por: Prabhu, Anusha, et al.
Publicado: (2021)

Optimising the consent process in severe traumatic brain injury trials
por: Murray, LJ, et al.
Publicado: (2011)

Understanding factors influencing questionnaire response rates to maximise retention in a long term complex intervention trial
por: Lane, Athene J, et al.
Publicado: (2011)

P269: Infection control practices during labor and delivery and newborn care in resource limited settings: assessment and recommendations for improvement
por: Huskins, WC, et al.
Publicado: (2013)

Use of deferred proxy consent in two emergency critical care trials
por: Kompanje, E, et al.
Publicado: (2009)

Retrospective consent in critical care: how achievable is it?
por: Carins, A, et al.
Publicado: (2015)

Successful approach for emergent consent for ECMO research
por: Board, J, et al.
Publicado: (2015)

Capacity building for critical care skills training provision in resource limited settings: the nursing intensive care skills training (nicst) project
por: Stephens, T, et al.
Publicado: (2015)

P41 Development of a Montgomery compliant consent discussion aide memoire leading to the establishment of a 'remote consent clinic'
por: Priestman, Elena, et al.
Publicado: (2021)

SWAT 84: effects of same-day consent vs delayed consent on the recruitment and retention of trial participants—an observational SWAT
por: Elfghi, M., et al.
Publicado: (2023)

Management of Lower Urinary Retention in a Limited Resource Setting
por: Ugare, U G, et al.
Publicado: (2014)

Feasibility and experience of using exception from informed consent in a pilot study of immediate estrogen infusion for hypotensive trauma patients
por: Wigginton, JG, et al.
Publicado: (2013)

Statistical inference in randomized consent designs in the presence of Hawthorne
por: Kim, Kyungmann
Publicado: (2015)

Participant Informed Consent in Cluster Randomized Trials: Review
por: Giraudeau, Bruno, et al.
Publicado: (2012)

Written Informed Consent for Participation in a Study and Reduction in Consent Rate
por: Tamakoshi, Akiko, et al.
Publicado: (2008)

P05.35. What are participants in clinical trials told about placebos? A content analysis of participant information leaflets
por: Bishop, F, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_boqkm4h7cctgedurmj7vgfnmfh