Evidence map›Paper›PMID 39538337›Full record

Trial reportTrials2024

Theoretically-informed vs standard cover letter to improve participant response to mailed questionnaire: results of an embedded randomised retention trial.

Colin C Everett, Sarah T Brown, Joanna L Dennett, Howard Collier, Claire L Davies, Frances Game, E Andrea Nelson

Abstract readRandomized Controlled TrialComparative Study
In one paragraph

Trial report in Trials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Swabs versus tissue samples for infected diabetic foot ulcers: the CODIFI2 RCT.Health technology assessment (Winchester, England) · 2025
    Trial
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

7 authors.

Colin C EverettClinical Trials Research Unit, Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK. colin.everett@manchester.ac.uk.ORCID http://orcid.org/0000-0002-9788-840X
Sarah T BrownClinical Trials Research Unit, Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK.ORCID http://orcid.org/0000-0002-1840-3786
Joanna L DennettClinical Trials Research Unit, Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK.ORCID http://orcid.org/0009-0009-1592-3119
Howard CollierClinical Trials Research Unit, Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK.ORCID http://orcid.org/0000-0002-0107-0604
Claire L DaviesClinical Trials Research Unit, Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK.ORCID http://orcid.org/0000-0002-7969-6738
Frances GameUniversity Hospitals of Derby and Burton NHS Foundation Trust, Derby, Derbyshire, UK.ORCID http://orcid.org/0000-0002-5294-4789
E Andrea NelsonGlasgow Caledonian University, Glasgow, Scotland, UK.ORCID http://orcid.org/0000-0001-6741-3078

Funding

Health Technology Assessment Programme 16/163/04
6 · The paper itself

Abstract

backgroundParticipant non-response is a source of bias in all research, especially in randomised controlled trials. Participants followed up remotely can have high non-response rates. Four such trials have been conducted of a cover letter with content informed by behaviour change theory to overcome hypothesised barriers to responding to a mailed questionnaire. Pooled results to date have suggested further research to be worthwhile. We conducted an embedded randomised study within a trial of such cover letters in the hope that we would improve response rates to our postal quality of life questionnaires.

methodsOne hundred forty-eight participants in the CODIFI2 diabetic foot ulcer sampling trial were randomised 1:1 to receive one of two different cover letters at follow-up timepoints: either a standard cover letter accompanying their postal follow-up questionnaires or to an 'enhanced' (theory-informed) cover letter. Questionnaires were mailed at 39, 52 and (for some participants) 104 weeks post randomisation. Outcome measures were response to mailing at each timepoint. Analysis was restricted to those for whom a questionnaire and letter was issued. Owing to limited recruitment, a reduced analysis plan, comprising solely observed response rates and 95% confidence intervals for difference in response rates was followed. Post hoc, we added our week 52 results to an already-published meta-analysis.

resultsSixty-seven out of 74 enhanced cover letter group (Enhanced) and 67/74 standard cover letter group (Standard) participants who had not already died or withdrawn were sent their first mailing at 39 weeks. The 39-week response rates were 47/67 (70.1%) and 39/67 (58.2%) for Enhanced and Standard participants, respectively. At week 52, the response rates were 45/64 (70.3%) and 35/63 (55.6%) for Enhanced and Standard participants, respectively. At week 104, the response rates were 24/33 (72.7%) and 19/33 (57.6%) for the Enhanced and Standard participants, respectively. Adding our week 52 results to a published meta-analysis increased the pooled estimate of differences in response rates to 0.04 (- 0.01 to 0.09) favouring enhanced letters.

conclusionWhile this embedded randomised controlled trial observed greater response rates at all times among those randomised to the enhanced letter, the reduced sample size meant that these results are imprecise.

trial registrationISRCTN registry ISRCTN74929588. Registered on 5 March 2019.

Indexed as

Diabetic FootPostal ServiceQuality of LifeAgedCorrespondence as TopicFemaleHumansMaleMiddle AgedResearch SubjectsSurveys and QuestionnairesTime FactorsBehavioural change theoryDiabetic footEmbedded randomised controlled trialFollow-up studiesHealth careOutcome assessmentQuality of lifeRetention methodsStudy within a trialSurveys and questionnairesSWAT

Identifiers

PMID39538337
PMCPMC11562673

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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.