Evidence map›Paper›PMID 38508646›Full record

ArticleBMJ open2024

REST: a preoperative tailored sleep intervention for patients undergoing total knee replacement - feasibility study for a randomised controlled trial.

Wendy Bertram, Chris Penfold, Joel Glynn, Emma Johnson, Amanda Burston, Dane Rayment, Nicholas Howells, Simon White, Vikki Wylde, Rachael Gooberman-Hill and 2 more

Abstract read
In one paragraph

Article in BMJ open, 2024. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Article
  4. An empirical comparison of sleep-specific versus generic quality of life instruments among Australians with sleep disorders.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2024
    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

12 authors.

Wendy BertramMusculoskeletal Research Unit, University of Bristol Medical School, Bristol, UK wendy.bertram@bristol.ac.uk.ORCID 0000-0001-8234-2052
Chris PenfoldMusculoskeletal Research Unit, University of Bristol Medical School, Bristol, UK.ORCID 0000-0001-8654-353X
Joel GlynnUniversity of Bristol Medical School, Bristol, UK.
Emma JohnsonUniversity of Bristol Medical School, Bristol, UK.
Amanda BurstonMusculoskeletal Research Unit, University of Bristol Medical School, Bristol, UK.
Dane RaymentNorth Bristol NHS Trust, Westbury on Trym, UK.
Nicholas HowellsNorth Bristol NHS Trust, Westbury on Trym, UK.
Simon WhiteCardiff and Vale University Health Board, Cardiff, UK.
Vikki WyldeMusculoskeletal Research Unit, University of Bristol Medical School, Bristol, UK.ORCID 0000-0002-8460-1529
Rachael Gooberman-HillNIHR Bristol Biomedical Research Centre, Bristol, UK.ORCID 0000-0003-3353-2882
Ashley BlomThe University of Sheffield, Sheffield, UK.
Katie WhaleMusculoskeletal Research Unit, University of Bristol Medical School, Bristol, UK.ORCID 0000-0002-0012-7103

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo test the feasibility of a randomised controlled trial (RCT) of a novel preoperative tailored sleep intervention for patients undergoing total knee replacement.

designFeasibility two-arm two-centre RCT using 1:1 randomisation with an embedded qualitative study.

settingTwo National Health Service (NHS) secondary care hospitals in England and Wales.

participantsPreoperative adult patients identified from total knee replacement waiting lists with disturbed sleep, defined as a score of 0-28 on the Sleep Condition Indicator questionnaire.

interventionThe REST intervention is a preoperative tailored sleep assessment and behavioural intervention package delivered by an Extended Scope Practitioner (ESP), with a follow-up phone call 4 weeks postintervention. All participants received usual care as provided by the participating NHS hospitals. OUTCOME MEASURES: The primary aim was to assess the feasibility of conducting a full trial. Patient-reported outcomes were assessed at baseline, 1-week presurgery, and 3 months postsurgery. Data collected to determine feasibility included the number of eligible patients, recruitment rates and intervention adherence. Qualitative work explored the acceptability of the study processes and intervention delivery through interviews with ESPs and patients.

resultsScreening packs were posted to 378 patients and 57 patients were randomised. Of those randomised, 20 had surgery within the study timelines. An appointment was attended by 25/28 (89%) of participants randomised to the intervention. Follow-up outcomes measures were completed by 40/57 (70%) of participants presurgery and 15/57 (26%) postsurgery. Where outcome measures were completed, data completion rates were 80% or higher for outcomes at all time points, apart from the painDETECT: 86% complete at baseline, 72% at presurgery and 67% postsurgery. Interviews indicated that most participants found the study processes and intervention acceptable.

conclusionsThis feasibility study has demonstrated that with some amendments to processes and design, an RCT to evaluate the clinical and cost-effectiveness of the REST intervention is feasible. TRIAL REGISTRATION NUMBER: ISRCTN14233189.

Indexed as

Arthroplasty, Replacement, KneeAdultBehavior TherapyCost-Benefit AnalysisEnglandFeasibility StudiesHumansRandomized Controlled Trials as TopicSurveys and Questionnairesfeasibility studieskneesleep medicine

Identifiers

PMID38508646
PMCPMC10961562

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.