Evidence map›Paper›PMID 28213595›Full record

Trial reportBMJ open2017

Qualitative study of the BREATHER trial (Short Cycle antiretroviral therapy): is it acceptable to young people living with HIV?

Sarah Bernays, Sara Paparini, Janet Seeley, Stella Namukwaya Kihika, Diana Gibb, Tim Rhodes

Open access · goldAbstract readClinical Trial, Phase IIEquivalence TrialMulticenter Study
In one paragraph

Trial report in BMJ open, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Time to Switch to Second-line Antiretroviral Therapy in Children With Human Immunodeficiency Virus in Europe and Thailand.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2018
    Observational
  8. Article
  9. 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

6 authors at 4 institutions in 2 countries.

Sarah BernaysFaculty of Public Health Policy, London School of Hygiene & Tropical Medicine, London, UK.
Sara PapariniFaculty of Public Health Policy, London School of Hygiene & Tropical Medicine, London, UK.
Janet SeeleyFaculty of Public Health Policy, London School of Hygiene & Tropical Medicine, London, UK.
Stella Namukwaya KihikaMRC/UVRI Uganda Research Unit on AIDS, Social Science Programme, Entebbe, Uganda.
Diana GibbMRC Clinical Trials Unit at UCL, London, UK.
Tim RhodesFaculty of Public Health Policy, London School of Hygiene & Tropical Medicine, London, UK.
London School of Hygiene & Tropical Medicine · GBUganda Virus Research Institute · UGFaculty of Public Health · GBUniversity College London · GB

Funding

Department of Health 08/53/25Medical Research Council MC_UP_A910_1114Medical Research Council MC_UU_12023/17Medical Research Council MC_UU_12023/26
6 · The paper itself

Abstract

objectivesA qualitative study of the BREATHER (PENTA 16) randomised clinical trial, which compared virological control of Short Cycle Therapy (SCT) (5 days on: 2 days off) with continuous efavirenz (EFV)-based antiretroviral therapy (CT) in children and young people (aged 8-24) living with HIV with viral load <50 c/mL to examine adaptation, acceptability and experience of SCT to inform intervention development.

settingPaediatric HIV clinics in the UK (2), Ireland (1), the USA (1) and Uganda (1).

participantsAll BREATHER trial participants who were over the age of 10 and aware of their HIV diagnosis were invited to participate. 49 young people from both arms of the BREATHER trial (31 females and 18 males; 40% of the total trial population in the respective sites; age range 11-24) gave additional consent to participate in the qualitative study.

resultsYoung people from both trial arms had initial concerns about the impact of SCT on their health and adherence, but these decreased over the early months in the trial. Young people randomised to SCT reported preference for SCT compared with CT pre-trial. Attitudes to SCT did not vary greatly by gender or country. Once short-term adaptation challenges were overcome, SCT was positively described as reducing impact of side effects, easing the pressure to carry and remember medication and enabling more weekend social activities. Young people on both arms reported frequent medication side effects and occasional missed doses that they had rarely voiced to clinical staff. Participants liked SCT by trial end but were concerned that peers who had most problems adhering could find SCT disruptive and difficult to manage.

conclusionsTo realise the potential of SCT (and mitigate possible risks of longer interruptions), careful dissemination and communication post-trial is needed. SCT should be provided alongside a package of monitoring, support and education over 3 months to allow adaptation. TRIAL REGISTRATION NUMBER: NCT 01641016.

Indexed as

Patient Acceptance of Health CareAdolescentAlkynesAnti-HIV AgentsBenzoxazinesChildCyclopropanesDrug Administration ScheduleDrug Therapy, CombinationFemaleHIV InfectionsHumansLongitudinal StudiesMaleMedication AdherenceQualitative ResearchAlkynesAnti-HIV AgentsBenzoxazinesCyclopropanesefavirenzantiretroviral therapyHIVPAEDIATRICS

Identifiers

PMID28213595
PMCPMC5318557
OpenAlexW2588665041

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.