Women’s and midwives’ views on the optimum process for informed consent for research in a feasibility study involving an intrapartum intervention: a qualitative study
Abstract Background Recruitment to intrapartum research is complex. Women are expected to understand unfamiliar terminology and assess potential harm versus benefit to their baby and themselves, often when an urgent intervention is required. Time pressures of intrapartum interventions are a major ch...
Main Authors: | Mary Alvarez, Emily J. Hotton, Sam Harding, Jonathan Ives, Joanna F. Crofts, Julia Wade |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2023-06-01
|
Series: | Pilot and Feasibility Studies |
Subjects: | |
Online Access: | https://doi.org/10.1186/s40814-023-01330-1 |
Similar Items
-
Intrapartum ultrasound and mother acceptance: A study with informed consent and questionnaire
by: Antonio Malvasi, et al.
Published: (2023-12-01) -
Researchers’ Experiences of Obtaining Informed Consent to Participate in Human Research and Its Facilitating Factors: A Qualitative Study
by: Mohammad Abbasinia, et al.
Published: (2022-12-01) -
Seeking consent to genetic and genomic research in a rural Ghanaian setting: A qualitative study of the MalariaGEN experience
by: Tindana Paulina, et al.
Published: (2012-07-01) -
Ex utero intrapartum treatment
by: Swiss Medical Weekly
Published: (2007-05-01) -
Research ethics, consent and publication
by: Marc Cornock, et al.
Published: (2023-08-01)