The effect of postal questionnaire burden on response rate and answer patterns following admission to intensive care: a randomised controlled trial
© The Author(s). 2017
Received: 30 August 2016
Accepted: 2 March 2017
Published: 27 March 2017
The effects of postal questionnaire burden on return rates and answers given are unclear following treatment on an intensive care unit (ICU). We aimed to establish the effects of different postal questionnaire burdens on return rates and answers given.
Design: A parallel group randomised controlled trial. We assigned patients by computer-based randomisation to one of two questionnaire packs (Group A and Group B).
Setting: Patients from 26 ICUs in the United Kingdom.
Inclusion criteria: Patients who had received at least 24 h of level 3 care and were 16 years of age or older. Patients did not know that there were different questionnaire burdens. The study included 18,490 patients. 12,170 were eligible to be sent a questionnaire pack at 3 months. We sent 12,105 questionnaires (6112 to group A and 5993 to group B).
Interventions: The Group A pack contained demographic and EuroQol group 5 Dimensions 3 level (EQ-5D-3 L) questionnaires, making four questionnaire pages. The Group B pack also contained the Hospital Anxiety and Depression Score (HADS) and the Post-Traumatic Stress Disorder Check List-Civilian (PCL-C) questionnaires, making eight questionnaire pages in total.
Main outcome measure: Questionnaire return rate 3 months after ICU discharge by group.
In group A, 2466/6112 (40.3%) participants responded at 3 months. In group B 2315/ 5993 (38.6%) participants responded (difference 1.7% CI for difference 0–3.5% p = 0.053).
Group A reported better functionality than group B in the EQ-5D-3 L mobility (41% versus 37% reporting no problems p = 0.003) and anxiety/depression (59% versus 55% reporting no problems p = 0.017) domains.
In survivors of intensive care, questionnaire burden had no effect on return rates. However, questionnaire burden affected answers to the same questionnaire (EQ-5D-3 L).
ISRCTN69112866 (assigned 02/05/2006).
KeywordsHealth related quality of life EQ5D Questionnaire Response rate Randomised control trial Intensive care Critical care Survivors Multicentre study Critical illness Outcome assessment
Self-completed postal questionnaires provide a convenient, cost-effective method of measuring patient outcomes, avoiding travel for participants and researchers. However, non-participation has been increasing over time . If non-participation is not random, the sampled population may differ from the whole population and may affect the generalisability and usefulness of the results .
Many researchers have investigated methods of improving responses to postal questionnaires. Their findings have been extensively reviewed [3–6]. Varied methods such as using a package of communication strategies, teasers on envelopes, personalising the questionnaire, non-monetary incentives and making clear that the study is based at a university have all been found to improve response rates . Questionnaire burden may affect participation in self-completed postal questionnaires [5, 6]. It may also alter the answers given .
Changes in quality of life, mental and physical health occur after treatment on an Intensive Care Unit (ICU) [8–12]. In the Intensive Care Outcome Network (ICON) study we investigated quality of life, mental and physical health following treatment on an ICU using validated postal questionnaires. Whether questionnaire burden affects return rates or answers from patients after treatment on an ICU is unknown. In other hospitalised patient populations, we found two randomised studies, with conflicting results [7, 13].
We therefore undertook an early example of a Study Within a Trial (SWAT)  to investigate the effects of questionnaire burden on participation and answers.
We conducted a randomised controlled trial as a study within a trial (SWAT), within the ICON study. The ICON study assessed quality of life, the incidence of depression, and the incidence of post-traumatic stress disorder following at least 24 h treatment on an ICU; the protocol has been published . The study received national ethics approval (REC 06/Q1605/17) and local research governance approval was obtained at each centre.
Patients from 26 UK ICUs took part (1 university hospital, 6 university-affiliated hospitals and 19 district general hospitals). We gave all patients a letter introducing the study at ICU discharge: it explained that they might receive mail from the study team. Patients were eligible if they received level 3 care (as defined by the Intensive Care Society, London ) on an ICU for at least 24 h. We excluded patients if they were under 16 years old. We also excluded patients not registered with a general practitioner or of no fixed abode (factors anticipated to prevent follow-up in the study). We excluded patients taking part in another questionnaire follow-up study run by the same research office.
We used a pseudo-random number generator, built into GNU Libc (http://www.gnu.org/software/libc/), to allocate patients to a study group without restriction. Allocation occurred at the central research office at the point of enrolment.
The group A pack contained four questionnaire pages. The pack contained the one page EuroQol 5 dimensions 3 level (EQ-5D-3 L) questionnaire, two pages each containing a single visual analogue scale and a single page demographics questionnaire.
The group B pack contained eight questionnaire pages. In addition to the group A pack, it also contained a two page Hospital Anxiety and Depression Scale (HADS) questionnaire and a two page Post-traumatic stress disorder Check List– Civilian version (PCL-C) questionnaire.
The initial packs sent at 3 months contained a personally addressed letter inviting participation. The 3-month packs also contained a three-page study information leaflet and a consent form (required by the Ethics Committee).
Packs at 12 and 24 months contained a covering letter and the questionnaires, but no information leaflet or consent form. However, if patients did not receive a 3-month pack because they remained in hospital, the 12-month pack contained the initial letter, study information leaflet and consent form. Questionnaire content remained the same at 3, 12 and 24 months.
Participants were unaware that we were sending different questionnaire packs.
Both groups received questionnaire packs 3 months after ICU discharge. We sent further questionnaire packs at 12 and 24 months after ICU discharge to respondents who agreed to take part further. We sent repeat questionnaire packs if a reply did not arrive after 2 weeks. Repeat questionnaire packs were identical to the first pack other than slight changes to the wording of the letter that made it clear that this was a repeat mailing. We did not contact patients who spent over 75 days in hospital following their discharge from ICU at 3 months, instead these patients were first contacted at 12 months. Patients who remained in hospital at 12 months did not receive any follow up.
We checked survival with the patient’s registered general practitioner and the National Health Service clinical spine application before posting each questionnaire pack. If the general practitioner informed us that a participant would be unable to complete a questionnaire, we did not send a pack.
We printed all documents using a high quality laser printer. We printed the invitation letter on Oxford University headed paper. The trial coordinator signed each letter. We printed each questionnaire on different coloured paper and bound them with a removable clip. All pages were single-sided and numbered. We used uniform design, large font size and generous spacing. All packs contained a Freepost addressed envelope for questionnaire return. All packs included an ICON branded pen with an ICON-labelled tea bag as incentives; the tea bag label invited the participant to enjoy a cup of tea whilst completing the questionnaire. Participants could also complete the questionnaires by telephone with a trained researcher.
The primary outcome measure was the questionnaire return rate 3 months after ICU discharge, by group. For the first mailed pack we defined questionnaire return as a completed consent form agreeing to take part in the study and at least one questionnaire question or visual analogue scale completed and returned. For subsequent packs we defined questionnaire return as at least one questionnaire question or visual analogue scale completed and returned.
Secondary outcome measures were return rates at 12 and 24 months and the effect of questionnaire burden on the EQ-5D-3 L weighted index score and individual domain scores at 3 months after ICU discharge. We defined a valid response as completion of all questions within an instrument. We undertook a post-hoc analysis of missingness on the invalid returns.
The ICON study ran for 19 months before the randomised controlled trial started. During this time we sent 6028 patients the group B pack and a Short Form 36 version 2 (SF36v2—health related quality of life questionnaire) at 3 months. The 3 month questionnaire return rate was 36%. We assumed a similar return rate for group B packs sent in the trial. We estimated 18,000 patients would take part in the next 28 months (allowing for site changes). Assuming a similar mortality 75 days following discharge from ICU (32%), power of 90% and a significance level of 0.05, this sample size was sufficient to detect a 2.9% change in the return rate.
We used an electronic form reader (Teleform v10, Cambridge, UK) to transcribe questionnaire responses into a database (MySQL v5.0-Oracle Corporation, Redwood Shores, CA). Study office personnel manually entered data that the electronic form reader could not interpret. We linked participant records with the Intensive Care National Audit & Research Centre (ICNARC) Case Mix Programme database to obtain admitting diagnoses and severity of illness scores .
Statistical analysis was undertaken using R Core v3.2.3 . We used Fisher’s exact test to compare between group rates of questionnaire return. We analysed questionnaire return rates for all patients to whom we sent a questionnaire. We used the Mann–Whitney “U” test to compare EQ-5D-3 L weighted index scores and visual analogue scales between groups at the first time point. We used the Chi-squared test to compare the proportion of patients who responded as EQ-5D-3 L level 1 (“No problems”) with a single collapsed category for those who responded as level 2 (“moderate”) or level 3 (“severe”) . We did not correct for multiple testing. We did not include information from EQ-5D-3 L respondents with any missing or invalid domain responses in our analysis of responses to the EQ-5D-3 L questionnaire.
Group A (n = 9132)
Group B (n = 9002)
All (n = 18,134)
Male sex (%)
APACHE II score
ICU length of stay days median [IQR]
Hospital length of stay days median
Reason for ICU admission n (%)
Respiratory tract infection
Major vascular procedure
Large bowel tumour
Acute renal failure
Chronic obstructive pulmonary disease
Responders at 3 months
Group A (n = 2466)
Group B (n = 2315)
All (n = 4781)
Age median, [IQR]
Male sex (%)
APACHE II score median, [IQR]
ICU length of stay days median [IQR]
Hospital length of stay days median [IQR]
Reason for ICU admission n (%)
Respiratory tract infection
Major vascular procedure
Large bowel tumour
Acute renal failure
Chronic obstructive pulmonary disease
Self-reported demographics n (%)
Not usual (unspecified)
Current employment status
Prior employment status
Mental problems now
Mental problems prior
Three, 12 and 24 month response rates
Response Rate (%)
Absolute difference (%)
0.0 to 3.5
−1.7 to 3.4
−2.1 to 2.5
1.00 to 1.06
0.94 to 1.13
0.85 to 1.21
We randomised 18,134 of the 18,490 patients assessed for inclusion (see Fig. 1). 5410 patients died within 3 months of ICU discharge. We delayed follow-up until 12 months in 554 patients who spent over 75 days in hospital. 12,170 patients were eligible to receive a questionnaire pack at 3 months. Table 1 shows demographic data for all participants. Table 2 is a response analysis showing the characteristics of those patients that responded to the study at 3 months (an equivalent non-response analysis is included in Additional file 1: Table S1). Between the two groups responders were very similar, although, without correction for multiple testing, differences existed in self-reported university education and need for assistance. Table 3 shows response rates at 3, 12 and 24 months by group. Response rates were equivalent at all time points.
Three month questionnaire responses
EuroQol 5 Dimension 3 Level (EQ-5D-3 L)
n = 2399 (97)
n = 2263 (98)
p = 0.003a
p = 0.771a
p = 0.107a
p = 0.986a
p = 0.017a
EQ-5D-3 L weighted index score
p = 0.255
EuroQol Visual Analogue Scale (EQ VAS)
n = 2402 (97)
n = 2244 (97)
EQ VAS Score
p = 0.174
Halving the questionnaire burden had no effect on response rates. Most participants who returned a questionnaire at 3 months completed questionnaires at later follow-up points. The group sent the long questionnaire pack reported worse function in the “mobility” and “anxiety and depression” EQ-5D-3 L domains.
We believe our study is by far the largest randomised controlled trial of questionnaire burden. Our short questionnaire pack was the EQ-5D-3 L (four pages). The EQ-5D-3 L was the shortest validated quality of life questionnaire for patients recovering from critical illnesses. Our long questionnaire pack also contained HADS and PCL-C questionnaires (an extra four pages).
We believe we followed best practice for postal questionnaires [3, 5, 6, 20]. Packs included an ICON branded pen and teabag as non-monetary incentives. We used a non-financial incentive appropriate to the situation as these have evidence of benefit and because a financial incentive would have been too costly given the scale of our study [5, 21]. We used personalised letters headed on University of Oxford paper that detailed the patients name, address and their admission hospital [3, 5]. We printed each questionnaire on different coloured paper bound with a removable clip . We used a package of postal communications, including sending out 2 copies of the questionnaires . We used good data management practices to optimise our data capture. This included using only single-sided pages to ensure participants did not miss questions printed on the back of pages and numbering the pages . We used a large font size and generous spacing to facilitate responses from older patients .
Our study has limitations. We only contacted patients by post, limiting our findings to postal-only questionnaires. We stopped sending questionnaires to patients who did not respond at the previous mailing point, however recovery from critical illness may have increased responses over time. Additional telephone contact may have changed our results, although this took place very rarely. Our short questionnaire pack contained nine pages. Five of these pages were the letter, consent form and information leaflet. These pages were necessary as patients did not agree to take part before leaving hospital. Informed consent before discharge would have been a more complex approach. However, a (shorter) pack without these pages may have improved return rates .
Two studies have examined the effect of questionnaire burden in patients discharged from hospital [7, 13]. In the International Stroke trial more participants responded to a six question EuroQol instrument than the longer SF-36 questionnaire . Yet, this difference was not seen with Picker Patient Experience questionnaires of different lengths .
Three systematic reviews have assessed the effect of reducing questionnaire burden on return rates [3, 5, 6]. They all included participants who had not recently been in hospital. Two report an increase in return rates with decreased questionnaire burden [5, 6]. The most recent, restricted to clinical randomised controlled trials found only a marginal effect . In patients recovering from severe illness, return rates to postal questionnaires are variable [7–12].
In the International Stroke Trial , where return rates were higher than in our study, patients agreed to take part in the trial before they received questionnaires. In the ICON study, we combined agreeing to take part and returning the first questionnaire. This combination may explain our lower initial return rates. Where patients agreed to take part in our study, later return rates were similarly high. In our study the longer questionnaire group reported worse function in the “mobility” and “usual activities” EQ-5D-3 L domains.
Two trials in recently hospitalised patients also studied the relationship between questionnaire burden and the answers given. Different Picker Patient Experience questionnaire lengths did not affect the answers given . Conversely, more stroke survivors scored themselves as dependent using the (shorter) six question EuroQol instrument than the SF-36 instrument . The difference seen may reflect the different questionnaires used, rather than the questionnaire burden. In our study, questionnaire burden affected the answers given to the EQ-5D-3 L questionnaire. When presented with additional questionnaires four percent of respondents placed themselves in a worse category.
In patients discharged from an ICU, our study is large enough to be definitive. Reducing questionnaire length from eight to four pages has little effect on return rates. However, including extra questionnaires resulted in different EQ-5D-3 L answers. This interaction suggests investigators should avoid mailings with multiple questionnaires. The effect adds to the case for minimising the burden to participants.
We undertook this study before the Study Within a Trial (SWAT) programme commenced [14, 23]. Our study demonstrates that large scale SWATs examining clinical outcomes can be undertaken. Our findings highlight the potential impact of trial methodologies on outcomes.
With the same response rate in the two groups, we did not expect different answers to EQ-5D-3 L domains. The reasons underlying the different answers remain unclear. The extra questions may have resulted in a different response group. Alternatively, the extra questions may have caused the same group to respond differently. We need to understand better the links between questionnaire burden and the pattern of answers.
In patients treated on an intensive care unit questionnaire burden affected the findings from the same questionnaire. This is a compelling reason to minimise the questionnaire burden. Halving the number of questionnaire pages had no effect on the return rate.
- EQ-5D-3 L:
EuroQol group 5 Dimensions 3 level
Hospital Anxiety and Depression Score
Intensive Care National Audit & Research Centre
Intensive Care Outcome Network
Intensive Care Unit
Post-Traumatic Stress Disorder Check List-Civilian
Research Ethics Committee
Short Form 36 version 2
Study Within a Trial
We would like to thank the following Intensive Care Units for taking part in this study: Bedford Hospital NHS Trust; Diana Princess of Wales Hospital, Grimsby; George Eliot Hospital NHS Trust, Nuneaton; Gloucester Hospital; Great Western Hospitals NHS Trust, Swindon; Hartlepool Hospital; Hemel Hempstead General Hospital; Hillingdon Hospital; James Cook University Hospital, Middlesbrough; James Paget Hospital, Great Yarmouth; Luton and Dunstable University Hospital; Medway NHS Foundation Trust, Gillingham; Nevill Hall Hospital, Abergavenny; New Cross Hospital, Wolverhampton; North Tees Hospital, Stockton-on-Tees; Oxford University Hospitals NHS FoundationTrust; Poole Hospital; Queen Mary’s Hospital, Sidcup; Royal Hampshire County Hospital, Winchester; Royal Lancaster NHS Trust; Russells Hall Hospital, Dudley; Southend NHS Trust, Westcliff-on-Sea; Stafford Hospital; The Royal Bournemouth and Christchurch NHS Trust; Trafford Hospital; Watford General Hospital.
We would also like to thank the Intensive Care National Audit & Research Centre (ICNARC) for providing data on patients included in the study. Finally we would like to thank Julie Darbyshire for proof-reading and improving the wording of the manuscript.
We thank Mr Barry Williams for more than fulfilling the role of patient representative on our trial steering committee. We are grateful to all those patients who kindly took part in our study whilst recovering from a significant period of ill-health.
Peter Watkinson affirms that this manuscript is an honest, accurate, and transparent account of the study being reported; that no important aspects of the study have been omitted; and that any discrepancies from the study as planned (and, if relevant, registered) have been explained.
The Oxford Radcliffe Hospitals NHS Trust (now the Oxford University Hospitals NHS Foundation Trust) sponsored the study but had no part in the conduct or analysis of the study.
The Intensive Care Outcomes Network study was funded by the Intensive Care Foundation and the BUPA Foundation. Peter Watkinson is supported by the Oxford Biomedical Research Centre.
Availability of data and materials
The anonymised dataset is available from the corresponding author. We did not obtain consent for data sharing, so we will only make anonymised data available.
RH helped design the study, developed and maintained the systems for data collection, prepared the data for analysis, undertook data analysis and wrote the initial draft of the paper. DY conceived the study, oversaw trial management and revised the paper. VB helped design the study, undertook trial management and revised the paper. DH took part in data analysis and study oversight, undertook the data linkage and revised the paper. PW took part in managing the trial, oversaw and took part in data analysis, substantially re-drafted and revised the paper, and is the guarantor. All authors read and approved the final manuscript.
All authors have completed the ICMJE uniform disclosure form at www.icmje.org/coi_disclosure.pdf and declare: no financial relationships with any organisations that might have an interest in the submitted work in the previous 3 years; no other relationships or activities that could appear to have influenced the submitted work.
Consent for publication
Ethics approval and consent to participate
This study was granted national ethics approval, Oxford Research Ethics Committee B (REC 06/Q1605/17). Informed written consent to participate in the study was obtained from all patients who chose to respond to a questionnaire.
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