Literature DB >> 19747269

Women's experiences of participating in the Magpie Trial: a postal survey in the United Kingdom.

Rebecca M D Smyth1, Lelia Duley, Ann Jacoby, Diana Elbourne.   

Abstract

BACKGROUND: The Magpie Trial compared magnesium sulfate with placebo for women with preeclampsia. The objective of this study was to explore women's views and experiences of participating in the Magpie Trial in the United Kingdom.
METHODS: Postal questionnaires were sent to 771 women participants in the Magpie Trial to assess long-term health of UK women and children. The questionnaire included three questions exploring women's experience of participating in the trial: (a) If time suddenly went backward, and you had to do it all over again, would you agree to participate in the Magpie Trial? (b) Please tell us if there was anything about the Magpie Trial that you think could have been done better; and (c) Please tell us if there was anything about the Magpie Trial, or your experience of joining the trial, that you think was particularly good.
RESULTS: Overall, 619 of the 771 women who were sent questionnaires returned them. In response to the three questions: (a) 58 percent (356) of women responded "definitely yes," 27 percent (169) "probably yes," 4 percent (23) "probably no," 5 percent (33) "definitely no," and 5 percent (34) "not sure." No clear evidence was shown of a relationship with allocated treatment, although women who responded "probably or definitely no" were more likely to have had side effects from trial treatment. (b) Although 44 percent of women stated that nothing could have been done better, free text suggestions related to content of recruitment information, and its timing, and wanting to know treatment allocation and trial results. c) Women were generally extremely positive about being followed up and receiving trial results.
CONCLUSIONS: Women were largely positive about participation in the trial and its follow-up, but still reported ways they believed the study could have been improved, such as more information, given earlier, which also has implications for clinical care.

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Year:  2009        PMID: 19747269     DOI: 10.1111/j.1523-536X.2009.00326.x

Source DB:  PubMed          Journal:  Birth        ISSN: 0730-7659            Impact factor:   3.689


  11 in total

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Authors:  A J Noble; A G Marson; C Tudur-Smith; M Morgan; D A Hughes; S Goodacre; L Ridsdale
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2.  Clinicians' views and experiences of offering two alternative consent pathways for participation in a preterm intrapartum trial: a qualitative study.

Authors:  Celine Y Chhoa; Alexandra Sawyer; Susan Ayers; Angela Pushpa-Rajah; Lelia Duley
Journal:  Trials       Date:  2017-04-26       Impact factor: 2.279

3.  Magpie Trial in the UK: methods and additional data for women and children at 2 years following pregnancy complicated by pre-eclampsia.

Authors:  Rebecca M D Smyth; Patsy Spark; Nina Armstrong; Lelia Duley
Journal:  BMC Pregnancy Childbirth       Date:  2009-04-14       Impact factor: 3.007

4.  Developing a survey of barriers and facilitators to recruitment in randomized controlled trials.

Authors:  Geetinder Kaur; Rosalind L Smyth; Paula Williamson
Journal:  Trials       Date:  2012-11-21       Impact factor: 2.279

5.  Experiences of recruiting to a pilot trial of Cardiac Rehabilitation In patients with Bowel cancer (CRIB) with an embedded process evaluation: lessons learned to improve recruitment.

Authors:  Gill Hubbard; Anna Campbell; Zoe Davies; Julie Munro; Aileen V Ireland; Stephen Leslie; Angus Jm Watson; Shaun Treweek
Journal:  Pilot Feasibility Stud       Date:  2015-04-14

6.  Women's views and experiences of two alternative consent pathways for participation in a preterm intrapartum trial: a qualitative study.

Authors:  Alexandra Sawyer; Celine Chhoa; Susan Ayers; Angela Pushpa-Rajah; Lelia Duley
Journal:  Trials       Date:  2017-09-09       Impact factor: 2.279

7.  Seizure First Aid Training For people with Epilepsy (SAFE) frequently attending emergency departments and their significant others: results of a UK multi-centre randomised controlled pilot trial.

Authors:  Adam J Noble; Dee Snape; Sarah Nevitt; Emily A Holmes; Myfanwy Morgan; Catrin Tudur-Smith; Dyfrig A Hughes; Mark Buchanan; Jane McVicar; Elizabeth MacCallum; Steve Goodacre; Leone Ridsdale; Anthony G Marson
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Review 9.  The ethical issues regarding consent to clinical trials with pre-term or sick neonates: a systematic review (framework synthesis) of the empirical research.

Authors:  E Wilman; C Megone; S Oliver; L Duley; G Gyte; J M Wright
Journal:  Trials       Date:  2015-11-04       Impact factor: 2.279

10.  Reduced fetal movement intervention Trial-2 (ReMIT-2): protocol for a pilot randomised controlled trial of standard care informed by the result of a placental growth factor (PlGF) blood test versus standard care alone in women presenting with reduced fetal movement at or after 36+ 0 weeks gestation.

Authors:  Lindsay Armstrong-Buisseret; Eleanor Mitchell; Trish Hepburn; Lelia Duley; Jim G Thornton; Tracy E Roberts; Claire Storey; Rebecca Smyth; Alexander E P Heazell
Journal:  Trials       Date:  2018-10-01       Impact factor: 2.279

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