Evidence map›Paper›PMID 31672711›Full record

ArticleBMJ open2019

Pragmatic cluster randomised cohort cross-over trial to determine the effectiveness of bridging from emergency to regular contraception: the Bridge-It study protocol.

Sharon Tracey Cameron, Paula Baraitser, Anna Glasier, Lisa McDaid, John Norrie, Andrew Radley, Judith M Stephenson, James Trussell, Claire Battison, Sarah Cameron and 11 more

Open access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors at 9 institutions in 2 countries.

Sharon Tracey CameronObstetrics and Gynaecology, University of Edinburgh, Edinburgh, UK sharon.cameron@ed.ac.uk.ORCID 0000-0002-1168-2276
Paula BaraitserDepartment of Sexual Health, King's College Hospital NHS Foundation Trust, London, UK.
Anna GlasierObstetrics and Gynaecology, University of Edinburgh, Edinburgh, UK.
Lisa McDaidMRC/CSO Social and Public Health Sciences Unit, University of Glasgow, Glasgow, UK.
John NorrieEdinburgh Clinical Trials Unit, Usher Institute, University of Edinburgh, Edinburgh, UK.
Andrew RadleyDirectorate of Public Health, NHS Tayside, Dundee, UK.ORCID 0000-0003-4772-2388
Judith M StephensonUCL Elizabeth Garrett Anderson Institute for Women's Health, University College London, London, UK.
James TrussellOffice of Population Research, Princeton University, Princeton, New Jersey, USA.
Claire BattisonEdinburgh Clinical Trials Unit, Usher Institute, University of Edinburgh, Edinburgh, UK.
Sarah CameronHealth Services Research Unit, University of Aberdeen, Aberdeen, UK.
Kathleen CowleBoots UK Ltd, Edinburgh, UK.
Mark ForrestHealth Services Research Unit, University of Aberdeen, Aberdeen, UK.
Richard GilsonInstitute for Global Health, University College London, London, UK.
Beatriz GoulaoHealth Services Research Unit, University of Aberdeen, Aberdeen, UK.
Anne JohnstoneObstetrics and Gynaecology, University of Edinburgh, Edinburgh, UK.
Alison McDonaldHealth Services Research Unit, University of Aberdeen, Aberdeen, UK.
Alessandra MorelliDepartment of Sexual Health, King's College Hospital NHS Foundation Trust, London, UK.ORCID 0000-0002-9803-2136
Susan PattersonMRC/CSO Social and Public Health Sciences Unit, University of Glasgow, Glasgow, UK.
Deirdre SallyInstitute for Global Health, University College London, London, UK.
Nicola StewartInstitute for Global Health, University College London, London, UK.
Bridge-It Study Group
NHS Lothian · GBUniversity of Aberdeen · GBKing's College Hospital NHS Foundation Trust · GBMRC/CSO Social and Public Health Sciences Unit · GBUniversity College London · GBUniversity College Hospital · GBNHS Tayside · GBPrinceton University · USWalgreens Boots Alliance (United Kingdom) · GB

Funding

Chief Scientist Office HSRU1Chief Scientist Office HSRU2Department of Health HTA/15/113/01Medical Research Council MC_UU_12017/2
6 · The paper itself

Abstract

introductionOral emergency contraception (EC) can prevent unintended pregnancy but it is important to start a regular method of contraception. Women in the UK usually access EC from a pharmacy but then need a subsequent appointment with a general practitioner or a sexual and reproductive health (SRH) service to access regular contraception. Unintended pregnancies can occur during this time. METHODS AND ANALYSIS: Bridge-It is a pragmatic cluster randomised cohort cross-over trial designed to determine whether pharmacist provision of a bridging supply of a progestogen-only pill (POP) plus rapid access to a local SRH clinic, results in increased uptake of effective contraception and prevents more unintended pregnancies than provision of EC alone. Bridge-It involves 31 pharmacies in three UK regions (London, Lothian and Tayside) aiming to recruit 626-737 women. Pharmacies will give EC (levonorgestrel) according to normal practice and recruit women to both intervention and the control phases of the study. In the intervention phase, pharmacists will provide the POP (desogestrel) and offer rapid access to an SRH clinic. In the control phase, pharmacists will advise women to attend a contraceptive provider for contraception (standard care).Women will be asked 4 months later about contraceptive use. Data linkage to abortion registries will provide abortion rates over 12 months. The sample size is calculated on the primary outcome of effective contraception use at 4 months (yes/no) with 90% power and a 5% level of significance. Abortion rates will be an exploratory secondary analysis. Process evaluation includes interviews with pharmacists, SRH clinicians and women. Cost-effectiveness analysis will use a healthcare system perspective and be expressed as incremental cost-effectiveness ratio. ETHICS AND DISSEMINATION: Ethical approval was received from South East Scotland REC June 2017. Results will be published in peer-reviewed journals and conference presentations. TRIAL REGISTRATION NUMBER: ISRCTN70616901.

Indexed as

Abortion, InducedAdultContraception BehaviorContraception, PostcoitalContraceptive Agents, FemaleCross-Over StudiesDesogestrelFemaleHumansLevonorgestrelPharmacyPilot ProjectsPragmatic Clinical Trials as TopicPregnancyPregnancy, UnplannedProgestinsContraceptive Agents, FemaleDesogestrelLevonorgestrelProgestinscontraceptionemergency contraceptionlevonorgestrelpharmacyprogestogen only pillunintended pregnancy

Identifiers

PMID31672711
PMCPMC6830607
OpenAlexW2982356072

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.