| Literature DB >> 33008059 |
Monika Grabia1, Renata Markiewicz-Żukowska1, Anna Puścion-Jakubik1, Joanna Bielecka1, Patryk Nowakowski1, Krystyna Gromkowska-Kępka1, Konrad Mielcarek1, Katarzyna Socha1.
Abstract
COVID-19 related restrictions aimed at curbing the spread of the coronavirus result in changes in daily routines and physical activity which can have a negative effect on eating and health habits. The aim of the study was to assess the impact of the COVID-19 pandemic on patients with diabetes and their nutrition and health behaviours. A survey conducted in July 2020 included 124 individuals with type 1 (n = 90) and 2 (n = 34) diabetes mellitus from Poland. To assess nutritional and health behaviours, an online questionnaire covering basic information, anthropometric data, and details regarding physical activity, eating, and hygiene habits was used. Almost 40% of all respondents with type 1 and 2 diabetes mellitus (DM) stated that their disease self-management had significantly improved. Over 60% of all participants declared that they had started eating more nutritious and regular meals during the COVID-19 pandemic. Enhanced hygiene, in particular, during the period, a statistically significant increase in hand sanitiser use was reported by respondents (18% vs. 82%, p < 0.001). The study demonstrated that the pandemic had a significant impact on the behaviour of patients with DM. Improved disease self-management and making healthy, informed food and hygiene choices were observed.Entities:
Keywords: COVID-19; diabetes mellitus; eating behaviours; food choices; hygiene; lifestyle habits; nutrition; sleep; stress; survey
Mesh:
Year: 2020 PMID: 33008059 PMCID: PMC7600117 DOI: 10.3390/nu12103013
Source DB: PubMed Journal: Nutrients ISSN: 2072-6643 Impact factor: 5.717
Baseline characteristics of study groups.
| Baseline Characteristics of Study Groups | T1DM | T2DM | ||||
|---|---|---|---|---|---|---|
| Total | Women | Men | Total | Women | Men | |
| Age (years) | 20A** | 20B** | 19 | 37.0A** | 37.5B** | 31.5 |
| Body weight (kg) | 65A** | 63B** | 75 | 75.0A** | 73.5B** | 78 |
| Height (cm) | 168 | 168 | 180 | 168 | 165 | 182.5 |
| Body mass index (kg/m2) | 22.7A** | 22.0B** | 22.9 | 26.1A** | 27.0B** | 23.3 |
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| ||||||
| Kindergarten and primary school | 17% (15) | 14% (11) | 27% (4) | - | - | - |
| Secondary school | 34% (31) | 36% (27) | 27% (4) | 21% (7) | 10% (3) | 67% (4) |
| University | 49% (44) | 50% (37) | 46% (7) | 79% (27) | 89% (25) | 33% (2) |
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| Village | 18% (16) | 16% (12) | 27% (4) | 24% (8) | 14% (4) | 67% (4) |
| City (≤150 k inhabitants) | 23% (21) | 28% (21) | - | 32% (11) | 39% (11) | - |
| City (150–250 k inhabitants) | 29% (26) | 25% (19) | 46% (7) | 20% (7) | 22% (6) | 17% (1) |
| City (≥250 k inhabitants) | 30% (27) | 31% (23) | 27% (4) | 24% (8) | 25% (7) | 17% (1) |
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| Up to 2 years | 15% (14) | 13% (10) | 27% (4) | 56% (19) | 53% (15) | 67% (4) |
| 2–5 years | 28% (25) | 28% (21) | 27% (4) | 29% (10) | 36% (10) | - |
| 5–10 years | 17% (15) | 17% (13) | 13% (2) | - | - | - |
| More than 10 years | 40% (36) | 42% (31) | 33% (5) | 15% (5) | 11% (3) | 33% (2) |
| HbA1c (%) D | 6.8 | 6.9 | 7.5 | 6.3 | 6.3 | 7.5 |
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| ||||||
| No change | 17% (15) | 20% (15) | - | 6% (2) | 7% (2) | - |
| Deteriorated | 47% (42) | 40% (30) | 80% (12) | 44% (15) | 46.5% (13) | 33% (2) |
| Improved | 37% (33) | 40% (30) | 20% (3) | 50% (17) | 46.5% (13) | 66% (4) |
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| No change | 28% (25) | 20% (16) | 60% (9) | 41% (14) | 43% (11) | 33% (2) |
| Increased ≤5 kg | 31% (28) | 34% (26) | 13% (2) | 18% (6) | 21% (6) | - |
| Increased >5 kg | 11% (10) | 13% (10) | - | 12% (4) | 7% (2) | 33% (2) |
| Decreased ≤5 kg | 23% (21) | 26% (17) | 27% (4) | 9% (3) | 11% (3) | - |
| Decreased >5 kg | 7% (6) | 7% (6) | - | 20% (7) | 18% (5) | 33% (2) |
Values are expressed as median, lower, and upper quartile (Me (Q1–Q3)) or percentage and number of respondents (% (n)). Abbreviations: Type 1 diabetes mellitus (T1DM) and type 2 diabetes mellitus (T2DM). A Statistically significant difference between the medians, T1DM vs. T2DM (the Mann–Whitney U test). B Statistically significant difference between the medians, women with T1DM vs. women with T2DM (the Mann–Whitney U test). C Statistically significant dependence between variables, T1DM vs. T2DM and women with T1DM vs. women with T2DM (the Chi-square test). D Results of the glycated haemoglobin (HbA1c) test were collected from 85% of respondents (type of diabetes mellitus: women/men), (T1DM 88%/73% and T2DM 86%/100%). * p < 0.05 and ** p < 0.001.
Characteristics of the subgroups, frequency of physical activity before and during the COVID-19 pandemic.
| Weekly Activity | Before/During the COVID-19 Pandemic | ||||||
|---|---|---|---|---|---|---|---|
| Total * | T1DM | T2DM | |||||
| Total * | Women * | Men | Total * | Women | Men | ||
|
| 21%/34% | 19%/33% | 22%/39% | -/7% | 26%/35% | 25%/35% | 33%/33% |
| 1–2 times/week | 36%/41% | 39%/42% | 40%/40% | 33%/53% | 26%/38% | 29%/39% | 17%/- |
| 3–4 times/week | 31%/19% | 30%/18% | 27%/17% | 47%/20% | 35%/24% | 39%/22% | 17%/33% |
| ≥5 times/week | 12%/6% | 12%/7% | 11%/4% | 20%/20% | 11%/3% | 7%/4% | 33%/33% |
Abbreviations: Type 1 diabetes mellitus (T1DM), type 2 diabetes mellitus (T2DM). Differences between “before” and “during” the COVID-19 period were evaluated by the Chi-square test (* p < 0.05).
Figure 1Differences between the type of physical activity “before” and “during” the COVID-19 pandemic. Differences between “before” and “during” the COVID-19 pandemic were evaluated by the Chi-square test (* p < 0.05 and ** p < 0.01).
Figure 2The impact of the COVID-19 pandemic on food and drink intake according to respondents’ responses.
Figure 3Frequency of hand washing/antibacterial agent use before and during the COVID-19 pandemic. Differences between “before” and “during” the COVID-19 period were evaluated by the Chi-square test (* p < 0.001).
Figure 4Stress level distribution before, at the beginning of the COVID-19 pandemic, and at the time of questionnaire completion.