Key summary points
To assess the feasibility of supplementing dietary nitrate (NO substrate) intake in care home residents.
AbstractSection FindingsExpressions of interest by care homes were not realised during the alpha COVID-19 wave of infections. Background dietary nitrate was < 30% of acceptable daily intake; most residents received a majority of their nitrate supplementation and supplementation increased urinary and salivary nitrate concentrations.
AbstractSection MessageRecruiting UK care homes during the COVID-19 pandemic was partially successful and supplemented dietary nitrate was tolerated and elevated urinary nitrate concentrations.
Abstract
Purpose
Infections cause considerable care home morbidity and mortality. Nitric oxide (NO) has broad-spectrum anti-viral, bacterial and yeast activity in vitro. We assessed the feasibility of supplementing dietary nitrate (NO substrate) intake in care home residents.
Methods
We performed a cluster-randomised placebo-controlled trial in UK residential and nursing care home residents and compared nitrate containing (400 mg) versus free (0 mg daily) beetroot juice given for 60 days. Outcomes comprised feasibility of recruitment, adherence, salivary and urinary nitrate, and ordinal infection/clinical events.
Results
Of 30 targeted care homes in late 2020, 16 expressed interest and only 6 participated. 49 residents were recruited (median 8 [interquartile range 7–12] per home), mean (standard deviation) age 82 (8) years, with proxy consent 41 (84%), advance directive for hospital non-admission 8 (16%) and ≥ 1 doses of COVID-19 vaccine 37 (82%). Background dietary nitrate was < 30% of acceptable daily intake. 34 (76%) residents received > 50% of juice. Residents randomised to nitrate vs placebo had higher urinary nitrate levels, median 50 [18–175] v 18 [10–50] mg/L, difference 25 [0–90]. Data paucity precluded clinical between-group comparisons; the outcome distribution was as follows: no infection 32 (67%), uncomplicated infection 0, infection requiring healthcare support 11 (23%), all-cause hospitalisation 5 (10%), all-cause mortality 0. Urinary tract infections were most common.
Conclusions
Recruiting UK care homes during the COVID-19 pandemic was partially successful. Supplemented dietary nitrate was tolerated and elevated urinary nitrate. Together, infections, hospitalisations and deaths occurred in 33% of residents over 60 days. A larger trial is now required.
Trial Registration
ISRCTN51124684. Application date 7/12/2020; assignment date 13/1/2021.
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Background
Epidemic winter infections due to viruses and bacteria cause considerable morbidity and mortality in care homes [1]. Common viral causes include influenza A/B viruses, parainfluenza virus, respiratory syncytial virus (RSV), rhinovirus and coronaviruses (CoVs: 229E, NL63, OC43, HKU1). Bacterial causes of respiratory infection include Chlamydia pneumoniae, Haemophilus influenzae, Legionella spp. and Streptococcus pneumoniae [1]. Care homes also have winter outbreaks of gastrointestinal tract infections (e.g. viral gastroenteritis due to norovirus), urinary tract, and skin and soft-tissue infections [1]. Overtaking all of these in 2020/21 was the SARS-CoV-2 pandemic which has had catastrophic consequences [2] with a third of excess deaths occurring in care homes and a reduction in resident life expectancy by 6 months [3]. Despite significant enhancements made to infection control procedures in care homes (hygiene, personal protective equipment) and prophylaxis with vaccination, infections have continued, and it is likely that event rates will return to baseline as practices normalise after the pandemic. Co-located older people in care homes are at high-risk for outbreaks of infectious diseases and yet there are no general antimicrobial measures that have demonstrated prophylactic efficacy against such outbreaks. For example, interventions such as probiotic capsules [4] have failed to demonstrate efficacy.
Nitric oxide (NO) possesses broad-spectrum antimicrobial activity with substantial in vitro and some in vivo data demonstrating anti-viral, bacterial, protozoal and fungi/yeast activity [5]. The antimicrobial effects of NO and derivative ions such as peroxynitrite are mediated by effects on RNA/DNA and protein conformation [5]. NO also improves organ blood supply and has pro-endothelial and anti-inflammatory and antithrombotic effects mediated through anti-leucocyte and anti-platelet activity [6], and these may also contribute to its antimicrobial effects. Antiviral and antibacterial activity has been demonstrated against many common causes of respiratory, gastrointestinal and soft-tissue infections; of relevance here, NO and phosphodiesterase 5-inhibitors (which maintain cyclic guanosine monophosphate levels, NO’s second messenger) have antiviral effects against influenza [7, 8] and coronaviruses such as SARS-CoV-2 [9, 10]. A recent human trial showed that a NO-nasal spray accelerated nasal SARS-CoV-2 viral clearance [11]. Endogenous NO is made from dietary amino acids (L-arginine and L-citrulline) and nitrate [5]. Phase II-equivalent clinical trials have supported anti-microbial effects of NO made from acidified nitrite on cutaneous viral and bacterial infections, dietary nitrate on oral bacteria, and NO gas against some respiratory viral infections [5]. Further, NO has been shown to improve exercise performance and cognition in older people [12], potential benefits of relevance to care home residents. Although some common infections have vaccines available (e.g. influenza, SARS-CoV-2), many do not yet (e.g. RSV) and vaccinations may need to be combined with chemoprophylaxis for effective prevention, especially in a population where immunosenescence is normal [13, 14]. So, NO substrates and donors may be particularly relevant due to their potential generic antimicrobial effects, especially since resistance against NO appears to be rare [5] in contrast to that occurring with many specific antimicrobial agents [1].
Care home residents have low nitrate and nitrite intake, in part because care home food may be low in nitrate content whilst food wastage (food left on plates) is high. We hypothesised that high infection rates in care homes might reflect low dietary nitrate intake and supplementation might reduce infections. The design and preliminary results of BEET-Winter have been published as a pre-print [15].
Methods
Aim, design and setting
BEET-Winter was a prospective cluster-randomised, placebo-controlled, blinded endpoint phase IIb trial and assessed pre-exposure prophylaxis; we tested the feasibility of supplementing dietary nitrate (given as beetroot juice) to care home residents, tolerability of beetroot juice, effect of dietary nitrate on salivary and urinary nitrate/nitrite concentrations, and safety and proof of concept. Further details are provided in the Supplementary Information and protocol on the trial website (https://stroke.nottingham.ac.uk/beet-winter/). The trial is registered ISRCTN51124684, application date 7/12/2020, assignment date 13/1/2021.
Rationale
The proposed trial was premised on the following: (i) NO has broad spectrum antimicrobial affects [5] and so may reduce infections and their severity including death; (ii) Dietary sources of NO have a very low risk of harm; (iii) Care home diets are low in dietary nitrate; (iv) SARS-CoV-2, respiratory epidemic and norovirus infections in care homes increase during the autumn, winter and spring months; (v) The symptoms of many respiratory infections overlap so it is not possible to reliably distinguish clinically between the causative organism (e.g. influenza virus vs. RSV vs SARS-CoV-2) in the absence of multiplex testing, which is not routinely deployed; (vi) Co-infections caused by two or more pathogens of concern may interact in as yet undetermined ways; and (vii) Most COVID-19 trials have focussed on interventions that are unlikely to have beneficial effects on other microbial pathogens.
Eligibility
UK care homes, with and without nursing or dual registered, were eligible for inclusion if they looked after older people, were rated at least ‘adequate’ by the English Care Quality Commission and had a minimum of 18 residents (Supplementary Information).
Randomisation and masking
As a cluster-randomised trial, care homes (and not residents) were randomised dynamically by computer algorithm using minimisation to balance across important baseline characteristics: type (without nursing vs dual registered or with nursing alone), prior SARS-CoV-2 infection in wave 1 of the pandemic, and size (≤ 32 vs > 32 residents). Ten percent of randomisations were based on chance. Randomised homes were assigned in a 1:1 ratio to receive nitrate-containing juice and usual care vs nitrate-free juice (placebo) and usual care. Residents, care homes and trials staff were unaware of the assigned treatments.
Interventions
Provision of nitric oxide (NO) was via 70 ml of nitrate-containing (400 mg) beetroot juice (Beet It Beetroot Juice Sport Shot—70 ml, James White Ltd, Ipswich UK), which is metabolised to NO in vivo, via the nitrate-nitrite-NO pathway [16] and was given once daily for 60 days. Placebo was given in the form of 70 ml of nitrate-free (0 mg) beetroot juice (placebo Beet It Beetroot Juice Sport Shot—70 ml, James White Ltd) given once daily for 60 days.
Both active and placebo juices have been used in multiple previous clinical trials and are identical in appearance, smell and taste [17]. Both juices contain folate, potassium, vitamin C, fibre and antioxidants but no allergens, and can be stored at room temperature with a shelf life > 1 year. The juices are palatable to many, but if found unpalatable, taste can be masked by dilution in other juices, e.g. orange or apple juice, or consumption through a straw.
Outcome measures
Feasibility outcomes included the following: recruitment of care homes; recruitment of residents; adherence to the intervention (75% of residents take > 50%); ability to take juice; assessment of salivary and urinary nitrate concentrations (using Quantofix nitrate/nitrite, Camlab, Cambridge UK) at 60 days; ability to measure the ordinal outcome measure; assessment of incident infection rate using the ordinal outcome; and estimation of the intra-cluster correlation (ICC). Background dietary nitrate intake was assessed from care home menus and photographs of lunch before and after consumption (Supplementary Information).
The efficacy outcome was the most serious event occurring during treatment from an ordinal clinical scale comprising: (1) all-cause mortality, (2) all-cause hospitalisation, (3) infection with the resident remaining in the care home but needing healthcare support (e.g. from the general practitioner, 111 call, 999 call/paramedic), (4) infection with the resident remaining in the care home and not needing healthcare support, and (5) no infection, at 60 days after randomisation; a further analysis assessed this outcome at 90 days. Other outcomes included the components of the efficacy outcome, efficacy outcome in pre-specified subgroups, time to asymptomatic and symptomatic proven SARS-CoV-2 infection, time to first admission to hospital and its cause, time to death and its cause, frailty (clinical frailty scale, CFS) [18], disability (Barthel index), cognition (6-item test) and quality of life (EuroQoL, EQ-5D-5L; EuroQoL visual analogue scale, EQ-VAS). Safety outcomes comprised reported serious adverse events (SAEs) and adverse events (AEs) which exclude any events contributing to the clinical primary outcome, i.e., not involving an infection, requiring hospitalisation or leading to death; SAEs were defined as those requiring healthcare support (i.e., medically important) and AEs as those not requiring healthcare support.
Dietary nitrate/nitrite intake
Dietary nitrate and nitrite intake were estimated from eight lunch menus and 69 photographs of lunch plates before and after consumption from four residents in one participating care home. These data were supplemented by internet-uploaded menus from three other UK care homes. Combining all the gathered information and with a consensus agreement between three researchers (AA, AKK, HJL), a representative 4-days’ full food and drinks menu, with serving sizes, was created for the care homes. Results were adjusted for average food wastage using data previously reported for a care home in the UK [19].
Procedures
Trial documents including protocol and training materials are hosted on an open website (https://stroke.nottingham.ac.uk/beet-winter/). Care Home staff were trained by the research trial team and then approached eligible care home residents for electronic informed consent, or relatives if the resident lacked capacity. Capacity was assessed using the ‘3 question approach’, as used in the RIGHT-2 trial [20].
Following consent/proxy consent, care home staff submitted data online (REDCap, Vanderbilt University, Nashville USA) at days 0 (baseline), 14, 60 (end-of-treatment) and 90 (final follow-up), and at the time of any outcome event or serious adverse event.
Statistical analysis
The statistical analysis plan was published on 9 August 2021 at https://stroke.nottingham.ac.uk/beet-winter/. A total of 360 residents from 30 homes with 12 residents per home (range 12–17) would be needed assuming alpha 0.05, power 0.80, intra-cluster correlation (ICC) 0.01 (with assumptions based on previous studies, Supplementary Information Table 1). Up to six additional care homes, each with between 4 and 20 participants, could be added in case some homes dropped-out, or if fewer than 12 residents were recruited at some homes.
Care home and resident characteristics and feasibility data are tabulated as number (%), median [interquartile range] or mean (standard deviation). Comparative analyses were to use a multi-level ordinal logistic regression model with adjustment for the minimisation factors and individual-level covariates (age, sex) and a random effect to adjust for clustering within care homes. The treatment comparison was to be presented as an adjusted common odds ratio (with 95% confidence intervals) for a shift in the direction of a better outcome on the ordinal scale [21]. Prespecified analyses of the efficacy outcome were to be performed in subgroups defined by the following adjustment factors: care home type (with/without nursing), prior SARS-CoV-2 infection in the care home, number of residents in care home, age, sex, vaccination status. Other outcomes were to be analysed using regression models dependent on data type (binary, categorical, continuous, time to event), adjusted similarly and accounting for clustering within care homes. All P values are two-sided and shown without adjustment for multiple testing. Analyses were performed using SAS version 9.4.
Results
Recruitment of care homes
Of an intended recruitment of 30 care homes, 16 expressed interest, 12 signed a contract, 7 received training, 6 consented residents and 5 treated and followed-up residents (Supplementary Information Tables 2 and 3, Fig. 1). Ethics submission was made via the UK Integrated Research application System (IRAS) system in mid-September 2020, i.e. prior to the start of the UK’s second COVID-19 wave (which was due to the wildtype/Wuhan variant) (Supplementary Information Table 4). However, the trial was subsequently rejected for urgent public health badging and so ethics review was not expedited; as a result, ethics approval was received in late November 2020 at the start of the UK’s third COVID-19 wave (due to alpha variant). Following contracting and training, the first care home was randomised in mid-December 2020 and started treatment in mid-January 2021. The trial timings are summarised in Supplementary Information Table 4. The median intervals between contact, contracting, juice testing, care home randomisation, training, juice arrival, consent, baseline assessment, start of juice and days 14, 60 and 90 are shown in Supplementary Information Table 5. Of the participating care homes, four were mixed or nursing and two had a CQC rating of excellent (Table 1).
Recruitment of residents
A total of 49 residents were recruited from six care homes, median 8.0 [7.0, 12.0] per home. Baseline characteristics were mostly balanced between the groups and were largely representative of UK care home residents in respect of mean (SD) age 82 (8) years, sex with 63% female and no non-whites (Table 1). A majority of residents (84%) lacked capacity to consent and needed consultee consent and 16% had an advance directive for non-admission to hospital. Residents mostly had the following: dementia (84%), maximal cognitive impairment (six-item test 28 of 28), frailty (CFS 7 of 9), dependency (BI 40/100) and poor quality of life (health status 0.5/1.0, visual analogue scale 65/100) (Table 1). Two care homes (with 6 participating residents) withdrew altogether from the trial following randomisation and prior to collection of baseline data or commencement of beetroot juice.
Adherence to beetroot juice
All 45 residents with data received at least one beetroot juice shot and 76% of residents took > 50% of drinks. The median [interquartile range] and (range) of drinks taken was, overall—40 [31, 47] (5–60), nitrate—46 [33, 58] (8–60) and placebo—32 [27, 43] (5–52).
Salivary/urinary nitrate concentration
Five of the six care homes reported at least some nitrate measurements. Baseline urinary nitrate concentration was 10 [10, 50] mg/L. Salivary measurements were not available from the two homes randomised to placebo; in those randomised to nitrate, the median [interquartile range] salivary nitrate was 50 [50, 100] mg/L and median [interquartile range] salivary nitrite [10, 20] mg/L (Supplementary Information Table 7). An on-treatment analysis based on randomised clusters was not possible due to the paucity of participating care homes. However, since dietary nitrate intake was low (Supplementary Information Table 7), salivary and urinary levels will largely have depended on randomised intake and so a comparison of residents on active versus placebo juice was performed without accounting for clustering. In before–after (baseline/day 60) analyses, those randomised to nitrate-containing beetroot juice had non-significantly higher urinary nitrate at 60 days, change 15 [0, 75] mg/L (p = 0.12); by contrast, levels did not change in those randomised to placebo juice, difference 9.5 [−10 to 40] (p = 0.33). When adjusted for baseline, urinary nitrate was higher with nitrate than no nitrate by 25 [0, 90] mg/L (p = 0.008), a more than doubling in concentration in the treatment group (Supplementary Information Table 7).
Clinical outcomes
Although we had originally intended to perform statistical comparisons between the randomised groups with adjustment for clustering on the basis that we had recruited 30 care homes, this plan was dropped when only six care homes followed up residents. As a result, the ICC was not estimated. Hence, we provide only descriptive results for the primary and secondary outcomes (Table 2). The ordinal primary outcome was measured in 48 of the 49 participating residents; a resident in a care home that only recruited one participant never received treatment or had follow-up performed. Following randomisation, no residents died during the 60 days of treatment, five (10%) were admitted to hospital, 11 (23%) had an infection with the resident remaining in the care home but needing healthcare support, none had an infection with the resident remaining in the care home and needing no healthcare support, and 32 (67%) had no infection (Table 2). A majority of infections were from the urinary tract with respiratory and cutaneous sources also present; no cases of COVID-19 or influenza were recorded. Causes for hospitalisation included infection, myocardial infarction, fall, need for thickener for dysphagia and having swallowed dentures. Secondary clinical outcomes were recorded in most residents at 60 days (Table 2).
Serious adverse events (SAEs) and adverse events were diverse in nature and were, with the exception of one AE, only reported by care homes randomised to nitrate (Table 3).
When assessed by individual care homes, it appeared that most primary outcome events, SAEs and AEs were reported by one home (labelled A, Table 4) that had been randomised to nitrate juice; two other homes randomised to nitrate reported few events (labelled B, C). Few clinical events were reported by the two homes randomised to nitrate-free juice (labelled E and F).
Dietary nitrate/nitrite intake
Taking account of food nitrate and nitrite content [22], nitrate content in drinking water and the World Health Organization nitrate acceptable daily intake (ADI) of 0.6 mmol/kg (3.7 mg/kg) body weight and nitrite of 0.0015 mmol/kg (0.07 mg/kg) [23,24,25], and assuming a 60 kg care home resident, mean dietary nitrate and nitrite intake were low at 29.8% and 10%, respectively (Table 2).
Vaccinations
Most (82%) residents had received one vaccination at baseline, and this rose to 96% by end of follow-up at day 90. Further, a majority (26, 57%) of residents had received double vaccination by day 90 (Supplementary Information Table 6). Both Astra-Zeneca and Pfizer vaccines were used. Almost all (44, 96%) residents had received influenza vaccination prior to baseline.
Trial challenges
Apart from lack of UPH badging and so delayed ethics approval, multiple other challenges occurred (Supplementary Information Table 8). Importantly, three care homes withdrew, one when the owner overruled the manager’s decision to participate and two when the manager left, and their replacement did not wish to participate. One of these care homes had already been randomised and received but not unpacked juice; for efficiency, the juice was passed onto the final recruited care home. At the care home level, two protocol violations occurred, with juice being started before consent in one and before baseline data had been collected in the other; these care homes were retrained on the key importance of consent and baseline data collection.
Four care home managers reported back on their experiences after trial end (Supplementary Information Table 9). Most felt it had been important to have taken part in the trial and that data collection volume was appropriate. All had diluted the beetroot juice in apple juice for reasons of palatability.
Discussion
Our study was designed to test the feasibility of performing a trial of nitrate supplementation to prevent infections in care homes and assess whether there was any signal of efficacy. Unfortunately, the trial failed to recruit the target of 30 care homes since its start was severely delayed during the autumn of 2020 and interested care homes withdrew. Nevertheless, some care homes and residents were recruited, beetroot juice was tolerated, and outcomes were recorded. Nitrate-containing beetroot juice significantly increased urinary nitrate and both salivary nitrate and nitrite concentrations in before-after analyses and, for urinary nitrate, when compared with placebo. However, the paucity of data precluded statistical analyses of the main outcomes and so proof of concept could not be tested. A majority of infections were localised to the urinary tract and no cases of COVID-19 or influenza were recorded, presumably reflecting high vaccination rates against these viruses.
The UK’s Urgent Public Health badging system has been lauded since it prioritised and made possible trials and other studies considered to have a reasonable probability of assessing the epidemiology of SARS-CoV-2 and of developing new treatments and diagnostics for COVID-19; examples include the VIVALDI [26] and CONDOR [27] studies in care homes and RECOVERY [28] trial in hospitals. However, the UPH system has also been criticised for preventing other COVID-19 related studies through lack of badging and delaying or abandoning of non-COVID-19 related research. The implication for BEET-Winter of not achieving UPH badging was to delay ethics approval by 7 weeks from late summer and before the second/wild-type wave to during the UK’s alpha wave of COVID-19 at which time care homes were focussing on protecting and caring for residents and managing staff sickness. Unsurprisingly, although a sufficient number of care homes had originally expressed interest, we were left with only 20% of these who delivered the trial. Hence, as a feasibility trial, BEET-Winter demonstrated that it was challenging to recruit during the pandemic without UPH badging; this system should be revised in any future pandemic so as not to prevent or delay studies from running. Since care home residents were disproportionately affected by COVID-19, it is unfortunate that we could not test an easy to administer dietary-based and inexpensive potential broad-spectrum anti-microbial agent. However, the impediments to starting should not apply outside a pandemic and so we anticipate that a trial testing the wider effects of dietary nitrate supplementation should be feasible.
Assessment of dietary nitrate intake using standard food composition tables is challenging [29], whilst recording dietary intake in nursing home residents is particularly demanding [30]. Nevertheless, care home residents appear to have a low dietary nitrate/nitrite intake that is less than 30% of acceptable daily intake, in part because high nitrate-containing foods such as leafy vegetables [22] are not prominent in menus and in part because food waste is high with leftovers on plates (14–25%) [19]. Hence, it is unsurprising that nitrate supplementation with beetroot juice significantly increased both salivary nitrate/nitrite and urinary nitrate concentrations, as has been reported previously in younger adults [31, 32]; such increases are likely to reflect higher plasma nitrate and nitrite concentrations [33]. In a recent study, survivors of COVID-19 infection had lower serum nitrite levels than a control uninfected group [34]. As has been seen in numerous trials in volunteers and older people with diabetes and hypertension, care home residents were largely adherent to both nitrate-containing and nitrate-free beetroot juice provided it was diluted in apple juice.
A key feasibility criterion was to collect infection, hospitalisation and fatal events and a third of residents had one of these. The paucity of data prevented us from comparing rates between the randomised groups. Further, many of these events as well as SAEs and AEs were reported by one home. Although event rates will vary between sites in any trial by chance, future trials will need to ensure thorough training so that common definitions of events are used and thus the propensity for differential reporting is reduced. Nevertheless, this observation does not detract from the possibility that dietary nitrate supplementation was associated with more events, SAEs and AEs, a question for a future trial.
Some of the technical difficulties faced with this trial replicate recurrent challenges seen in care home research. There is no care home research infrastructure in the UK outside of the Enabling Research in Care Homes (EnRICH) network [35], which focusses mainly on raising awareness of research and enabling co-operation with the care home sector. Care home staff are not routinely trained in Good Clinical Practice, many are research-naïve, and staff are substantially stretched to provide routine day-to-day care, even without the imposition of research. We have demonstrated with previous trials [36], and through this feasibility study, that these difficulties can be overcome through careful trial design. However, the superimposition of the COVID-19 pandemic rendered the research climate in care homes even more challenging with staff shortages, increased staff turnover and an increased burden of infection control activities that left even less time for research. We can reasonably assert that the objectives of this study would have been easier to achieve outside the context of the pandemic.
Having a cluster rather than individual randomised trial has both advantages and disadvantages. Cluster designs are especially relevant to care home trials since they reduce the risk of bias due to contamination [36], facilitate recruitment, enable the management and delivery of the intervention, and ease identification of serious adverse events in comparison with individual randomisation. Further, they most reflect the manner that prophylactic interventions will be used in care homes, i.e. for most residents. We have completed two cluster randomised trials in care homes, FICH [37] and FinCH [36, 38] and so elected to use a cluster trial design. Nevertheless, cluster randomisation leads to much larger trials than those using simple randomisation. In retrospect, it can be argued that we should have used individual randomisation with a resulting smaller sample size whilst accepting the relative weaknesses of this study design in a closed care home environment.
The strengths of this trial are the double-blind placebo-controlled design and assessment of resident dietary nitrate intake, juice tolerability in older people and effects on salivary and urinary nitrate/nitrite concentrations. Although long-term care sectors differ between countries, the COVID-19 pandemic has affected them similarly. If an evaluation of our intervention proved it to be effective, it is likely that such findings would be generalisable.
However, there are several caveats. First, we under-recruited care homes and so residents; this precluded statistical analysis that might have supported proof of concept. Second, there may have been differential care home reporting of outcomes and SAEs. Use of central routine data collection would remove this potential source of bias. Third, most reported infections were urinary tract infection, a notoriously unreliable diagnosis to make without laboratory support. Use of a multiplex approach might improve diagnosis and identification of the pathogen; a similar approach would help identification of microbes causing respiratory tract infection. Last, the use of a cluster design meant that far more care homes and residents were needed than if randomisation had been at the level of individuals.
Conclusions
In summary, BEET-Winter tested the hypothesis that enhancing dietary inorganic nitrate intake might reduce care home infection rates during the winter, including COVID-19 and influenza rates. The trial started later than planned and during an active phase of the COVID-19 pandemic so that too few care homes, and so residents, were recruited. As a result, we were not able to test proof of concept and will need to repeat this assessment. However, the low dietary nitrate intake seen in care homes and increase in salivary and urinary concentrations seen with supplementation mean that antimicrobial effects should be obvious if preclinical and phase II-equivalent evidence of the effect of NO donors on bacteria and viruses [5] translates clinically. Since NO donors have vasculoprotective effects, and potential benefits on cognition, a larger trial might include these in a combined outcome. Nevertheless, adequate training will need to be performed with care home staff to reduce differential reporting of outcomes and SAEs.
Data availability
The data are available from the corresponding author on reasonable request with a protocol including analysis plan.
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Acknowledgements
We thank the participating care homes, residents and their families who participated in and supported this trial.
Funding
The trial was co-funded by the Nottingham National Institute of Health Research (NIHR) Biomedical Research Centre and PMB’s NIHR Senior Investigator award. Beetroot juice was bought in bulk with discount from James White Ltd. The trial was coordinated by the Nottingham Stroke Trials Unit and sponsored by the University of Nottingham.
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PMB wrote the first draft of the manuscript; the other authors commented and revised this. PMB is Stroke Association Professor of Stroke Medicine and emeritus NIHR Senior Investigator. AM was a member of the NIHR urgent public health committee but withdrew from discussions about this trial. ALG is part-funded by the NIHR Applied Research Collaboration-East Midlands (ARC-EM).
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AJW holds shares in HeartBeet Ltd, which receive a royalty from James White Drinks Ltd who manufacture the active nitrate-containing beetroot juice and placebo nitrate-depleted juice used in this study. The remaining authors declare no competing interests.
Ethical approval
All methods were carried out in accordance with relevant guidelines and regulations. Approvals were sought via the UK Integrated Research Application System (IRAS project 288542), and favourable opinions received from Research Ethics Committee (West Midlands: Coventry & Warwickshire Research Ethics Committee—20/WM/0278, 19/11/20) and Health Research Authority (25/11/20). Approval from the UK Medicines and Healthcare products Regulatory Agency was not sought since beetroot juice is a food.
Informed consent
Written informed electronic consent (using the REDCap facility) was sought from residents if they had mental capacity to provide consent or from a family member consultee for residents who lacked capacity.
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Not applicable.
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Bath, P.M., Skinner, C.J.C., Bath, C.S. et al. Dietary nitrate supplementation for preventing and reducing the severity of winter infections, including COVID-19, in care homes (BEET-Winter): a randomised placebo-controlled feasibility trial. Eur Geriatr Med 13, 1343–1355 (2022). https://doi.org/10.1007/s41999-022-00714-5
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DOI: https://doi.org/10.1007/s41999-022-00714-5