key: cord-0746299-eppfugqm
authors: Himbert, Caroline; Hathaway, Cassandra A.; Daniels, Bailee; Salas, Karen; Ashworth, Anjelica; Gigic, Biljana; Lin, Tengda; Viskochil, Richard; Kirchhoff, Anne C.; Grossman, Douglas; Ose, Jennifer; Tward, Jonathan; Scaife, Courtney; Figueiredo, Jane C.; Toriola, Adetunji T.; Beck, Anna; Shibata, David; Gonzalez, Brian D.; Matsen, Cindy; Christenson, Cristina; Ma, Debra S.; Colman, Howard; Hunt, Jason P.; Jones, Kevin B.; Lee, Catherine J.; Larson, Mikaela; Onega, Tracy; Akerley, Wallace L.; Li, Christopher I.; Schneider, Martin; Penedo, Frank J.; Siegel, Erin M.; Tworoger, Shelley S.; Ulrich, Cornelia M.; Peoples, Anita R.
title: Impact of the COVID-19 pandemic on exercise habits among cancer patients
date: 2021-09-21
journal: Res Sq
DOI: 10.21203/rs.3.rs-704646/v1
sha: 3d496ec45f4616ef068c49ded5d1e3abf0b472e6
doc_id: 746299
cord_uid: eppfugqm

PURPOSE: There is limited information on how the COVID-19 pandemic has changed health behaviors among cancer patients. We examined the impact of the pandemic on changes in exercise behaviors and identified characteristics associated with these changes among cancer patients. METHODS: Cancer patients (n = 1,361) completed a survey from August-September 2020 to assess COVID-19 pandemic-related changes in health behaviors and psychosocial factors. Patients were categorized into 3 groups: exercising less, exercising did not change, and exercising more. Patient characteristics were compared by exercise groups. RESULTS: One-third of the patients reported a decreased amount of regular exercise, while 11% reported exercising more during the pandemic. Patients who exercised less were more likely to be unemployed/retired, undergoing active treatment, and had increased pandemic-related alcohol consumption and psychosocial stressors such as loneliness and financial stress (all p < 0.05). In contrast, patients who exercised more were younger, female, full-time employed, did not consume alcohol, and had good health status and more social interactions (all p < 0.05). Patients who were living in rural areas and did not experience changes in daily life, were also more likely not to experience changes in exercise habits (all p < 0.05). CONCLUSION: Our results indicate that a significant proportion of cancer patients experienced changes in exercise habits during the first 6 months of the COVID-19 pandemic. Age, sex, employment status, health status, alcohol consumption, and psychosocial factors were associated with changes in exercise behaviors. Providers should monitor for changes in health behaviors, such as exercise, because of their importance in improving cancer survivorship.

The COVID-19 pandemic has challenged healthcare in many ways by overwhelming healthcare capacities, delaying elective procedures, and overall, disrupting medical care (1) (2) (3) (4) . Long-term impacts of the pandemic within many healthcare disciplines are expected to emerge over the next years or even decades. Within cancer care and prevention, the pandemic has led to delays or deferrals of cancer-related treatments, screening, and surveillance appointments (5-10). For example, weekly colorectal cancer screenings drastically decreased by 86% in 2020 (6, 10, 11). As a result, an increase in more advanced stage cancer cases is expected to emerge in the upcoming years.

Many behavioral factors including physical activity have been established as risk and prognostic factors of cancer (12) (13) (14) (15) (16) . Collective evidence shows that increased physical activity levels throughout the cancer care continuum may decrease the risk of disease and extend survival, particularly among breast and colon cancer patients (12) (13) (14) (15) (16) . The American College of Sports Medicine reports that by following these guidelines mortality rates of high incident cancer types (e.g., breast, colon, and prostate cancer) may be reduced by 40 to 50% (17, 18) . Physical activity after cancer diagnosis has further shown to improve overall quality of life, fatigue, sleep, mental health including depression and anxiety, and immune responses (19) .

There is some evidence that the pandemic has led many individuals to change their health behaviors including physical activity levels and diet, potentially due to stay-at-home policies and closure of gyms (20-23). Experts are concerned that social isolation and COVID-19 restrictions will lead to physical inactivity among cancer survivors (24) . A recent study reported that physical activity levels measured in step counts signi cantly decreased within the general population since the start of the pandemic (20). Another study in breast cancer survivors showed that 90% of the study population reduced their physical activity levels and increased the amount of sedentary behavior (25) . This study in breast cancer patients is the only study to date among individuals with cancer to examine changes in exercise behaviors due to the pandemic. However, their ndings were limited by the small sample size (n = 37).

In the present study, we identify risk/protective factors for decreased physical activity among cancer patients and survivors. The results of this study will highlight the importance of promoting bene cial health behaviors, including exercise, among cancer patients and survivors especially during and post pandemic. Further, this work will allow clinicians and researchers to 1) know which subgroup of patients need early intervention to prevent decreased physical activity, and 2) identify modi able targets for future interventions (e.g., social interactions).

As part of the COVID-19 and Oncology Patient Experience Study (COPES) consortium, n = 1,477 adult cancer patients (≥ 18 years), who had visited Huntsman Cancer Institute (HCI) between 2016-2020 and were enrolled in the Total Cancer Care (TCC) study (NCT01091974), the ColoCare Study (NCT02328677), completed a COVID-19 survey (26-28). The majority of the patients at HCI completed the survey electronically, while some completed it in person or over the phone, between August and September 2020.

Response rates ranged from 14-57%. N = 1,361 patients diagnosed with stage I-IV cancers (n = 27 with stage 0 were excluded) and had data available on changes in exercise habits (n = 89 with missing data on exercise habits or who exclusively reported "exercising in a different location than normal" were excluded), were included in the present work. The University of Utah Institutional Review Board (IRB) approved this protocol, and all participants provided written informed consent.

Outcome:

Exercise habits (health behavior): A change in exercise habits was determined based on the following questions: 'Since the COVID-19 pandemic began (March 2020), have your exercise habits changed?' (yes or no)' and 'Since the COVID-19 pandemic began (March 2020), in what way have your exercise habits changed? Check all that apply' ('I do not exercise regularly', 'I am exercising less', 'I am exercising more', 'I am exercising in a different location than normal', and 'other'). Since the survey was administered between August and September 2020, the changes assessed in exercise habits were during the rst 6 months of the pandemic (March to August/September 2020). Ninety-two percent of patients (n = 1,361/1,477), who participated in the survey completed the questions on changes in exercise habits. Patients were categorized into three groups: exercise less i.e., patients who responded 'I do not exercise regularly' or 'I am exercising less;' exercise did not change i.e., patients who responded 'no' change in exercise habits; and exercise more i.e., patients who responded 'I am exercising more.' Patients who provided free-text responses under 'other' were categorized on an individual basis. However, patients who exclusively checked 'I am exercising in a different location than normal' were also excluded from the analyses.

Demographic and clinical characteristics Sociodemographic (sex, age, race, ethnicity) and clinical characteristics (tumor site, tumor stage) were abstracted from electronic medical records. Participants self-reported their body-mass index (BMI; if selfreported BMI was missing, it was abstracted from medical records), current cancer patient status, COVID-19 infection status, and employment status. A measure of overall health status was adapted from the 12item Short-Form Health Survey quality-of-life (QoL) measure (29) . Zip codes were categorized as urban or rural using the Rural-Urban Commuting Area Codes (RUCA) classi cation system (30) .

Smoking status was either self-reported (current or change in smoking status) or abstracted from medical records (ever smoker i.e., at least 100 cigarettes in their lifetime). Patients also self-reported their alcohol consumption in the past year as well as change in alcohol consumption since the COVID-19 pandemic started.

Psychosocial factors: Participants reported changes in daily life and nancial stress in past month on a Likert scale from 1 (not at all) to 5 (a lot/very much) (31) . Changes in social interaction were reported by participants on a scale from 1 (much less social interaction) to 5 (a lot more social interaction), which was classi ed as participants reporting either: fewer social interactions, no change in social interactions, and more social interactions. A single item "How often have you felt lonely in the last month?" scored on a scale of 1 (never) to 5 (always) was adapted from the NIH Toolbox Loneliness instrument assessing perceptions of loneliness, which is an aspect of social relationships (32) . An item from the Perceived Stress Scale was used to assess perceived stress, asking "In the last month, how often have you felt di culties were piling up so high that you could not overcome them?" and scored on a scale of 1 (never) to 5 (often) (33, 34) .

Descriptive statistics (frequencies and percentages for categorical variables and mean and standard deviations for continuous variables) were performed for all variables of interest. One-way analysis of variance (ANOVA) for continuous variables and χ-square tests for categorical variables were used to determine statistically signi cant differences (p < 0.05) between the three exercise behavior groups (exercise less, exercise did not change, exercise more). T-tests for continuous variables and χ-square tests for categorical variables were used to determine statistically signi cant differences (p < 0.05) between the two changes in exercise behavior groups (exercise more and less). Statistical analyses were performed using SAS Software version 9.4. Table 1 summarizes the patient characteristics for N = 1,361 cancer patients included in the present analyses. Mean age was 61 (range: 20-92) and 54% were female. The majority of patients had been diagnosed with breast (n = 156, 13%), gastrointestinal (n = 173, 15%), or hematologic cancers (n = 231, 19%). Over half were diagnosed with cancer stage I (37%) and II (25%). The patients had on average a BMI of 28.2 kg/m 2 . Most participants were residents from Utah and 26% lived in rural areas. About onethird of patients [n = 439 (32%)] reported that they exercised less, while 152 (11%) patients exercised more during the pandemic. Over half of the study population (57%) reported to not have changed their exercise habits since the pandemic. Changes in exercise habits by demographic and clinical characteristics Table 2 compares demographic and clinical characteristics by change in exercise habits. Patients who started exercising more during the pandemic were on average 5 years younger (mean age: 55 years) as compared to those who exercised less (mean age: 60 years) or did not change their exercise habits (mean age: 62 years) (p < 0.0001). Female patients appeared to be exercising more since the pandemic (64% exercising more vs. 56% exercising less, p = 0.08). Male patients were more likely to maintain their exercise behavior (44% exercising less vs. 50% did not change exercise vs. 36% exercising more). Patients who were full-time employed were less likely to exercise less (29%) or change their exercise habits (35%) as compared to exercising more (48%; p < 0.0001); while unemployed or retired patients were more likely to exercise less as compared to exercise more (63% vs. 42%; p < 0.0001). Patients who were able to maintain their exercise habits were more likely to be living in rural areas as compared to those exercising less or more (32% vs. 21% or 19%; p < 0.0001); on the other hand, a higher percentage of urban patients reported changes in their exercise habits i.e., they either exercised less (79%) or more (81%). were more likely to increase their exercise levels (59%) compared to exercising less (51%) and no changes in exercise behaviors (54%, p < 0.0001). Conversely, patients with the highest alcohol consumption (3-4 times a week to every day) either exercised less (18%) or did not change their exercise habits (16%) as compared to only 10% of those who exercised more (p = 0.001). Change in alcohol consumption due to the pandemic was associated with changes in exercise habits (p = 0.03). In particular, those who reported an increase in alcohol consumption due to the pandemic were also more likely to exercise less (7%) as compared to exercising more (4%) or reporting a change in their exercise habits (4%). Further, those who reported no change in alcohol consumption due to the pandemic were also more likely not to experience a change in their exercise habits (92%) as compared to exercising less (86%) or more (87%). Missing values due to skip patterns or non-response not shown (current smoking status: n = 15; alcohol consumption in the past year: n = 140; change in alcohol consumption habits since COVID pandemic: n = 208); a comparing 3 groups of changes in exercise habits; b comparing 2 groups of changes in exercise habits (exercise less vs. exercise more). Table 4 compares psychosocial factors by changes in exercise habits. The majority of patients (56%) experienced a moderate amount or a lot of changes in their daily life due to the pandemic. Patients who reported 'not at all' or 'a little bit' change in daily lives were also more likely to report no changes in their exercise habits (26%) as compared to exercising less (8%) or more (14%; p < 0.0001); there were no signi cant differences seen between exercising less and more groups (p = 0.14). Overall, most patients reported less social interactions in the past month (65%). Patients who reported more social interactions were more likely to exercise more as compared to exercising less or maintaining their exercise habits (p < 0.0001). Feeling lonely, di culties piling up, and nancial stress in the past month had similar trends by the exercise groups. Patients who 'never' felt lonely, 'never' had di culties piling up, or were 'not at all' nancially stressed were also more likely not to experience changes in their exercise habits during the pandemic as compared to those exercising less or more (p < 0.0001). Conversely, patients who regularly experienced loneliness, di culties piling up, or nancial stress also exercised less as compared to patients who exercised more or maintained their exercise habits (p < 0.0001). However, loneliness, di culties piling up, and nancial stress were not signi cantly different between exercising less and more groups (p = 0.48, 0.06, and 0.42, respectively). (7) Very much 23 (5) 27 (4) 3 (2) NOTE: Data might not add to 100% because of rounding.

Missing values due to skip patterns or non-response not shown (change in daily life due to pandemic: n = 1; change in social interaction in past month: n = 2; felt lonely in past month: n = 1; di culties piling up that could not be overcome in past month: n = 2; nancially stressed in past month: n = 1); a comparing 3 groups of changes in exercise habits; b comparing 2 groups of changes in exercise habits (exercise less vs. exercise more).

To the best of our knowledge, this is the rst large study to investigate changes in exercise behaviors among cancer patients during the rst 6 months of the COVID-19 pandemic as well as characteristics associated with these changes. One-third of our study population reported to have decreased the amount of regular exercise. Our results also indicate that age, employment status, overall health status, alcohol consumption, current patient status, and psychosocial factors were associated with changes in exercise behaviors during the pandemic.

A reduction in exercise is especially concerning in the cancer population given the strong evidence of bene cial effects of physical activity on survivorship (12-16, 19, 35) . Physical activity before and after cancer diagnosis has been shown to have substantial health bene ts for cancer patients (12-16, 19, 35) .

Physical activity not only reduces the risk of cancer but can also improve cancer outcomes, including survival and recurrence. (12-16, 19, 35) . Further, physical activity enhances overall quality of life and physical function particular among individuals with cancer, and may improve other potential comorbidities including diabetes, cardiovascular, or respiratory diseases (19) . Although not explicitly asked in this study, challenges in accessing exercise facilities, being at high risk of having poor outcomes if exposed to COVID-19 infection, or nding motivation to exercise due to stay-at-home policies may have contributed to the substantial decrease in exercise activities observed in this study.

Our study provides further support for prior research before the pandemic highlighting the barriers to exercise and determinants of exercise adherence among cancer survivors (36, 37). Older cancer survivors often engage in less activity due to underlying health conditions, a higher prevalence of overweight and obesity, cancer treatment-related side effects such as fatigue and pain (37) . Among cancer patients, adherence to exercise interventions does not appear to be in uenced by sex, although the data remains inconclusive (36). However, our results indicate that response to the pandemic with respect to increased physical activity was higher among female patients compared to those whose physical activity decreased. In alignment with previous studies showing that employed individuals spend more time in moderate and vigorous physical activity (38, 39), full-time employed patients in our study population were more likely to increase their activity levels since the start of the pandemic. Greater opportunities to workout while working from home and less time spent commuting may explain this observation. On the contrary, unemployed patients may be retired and older or may have lost job due to the pandemic and, hence, less active. Consistent with prior research, (40, 41) urban patients in our study experienced more changes in their exercise habits due to the pandemic, potentially due to stay-at-home policies, closure of gyms, or more time to workout (42, 43) .

Our study indicates that patients diagnosed with lung cancer or hematologic neoplasms were more likely to increase exercise during the pandemic, while patients diagnosed with gastrointestinal cancers and melanoma were more likely to decrease exercise than increase or maintain it. This aligns with studies conducted before the pandemic showing reduced engagement in physical activity among patients with gastrointestinal cancer (44, 45) . Melanoma patients are also more likely to avoid outdoor activities to minimize sun exposure (46), which may explain reduced exercise levels due to closure of gyms with outdoor exercise being the only alternative. Our data suggest that patients with stage IV disease tend to exercise more. Exercise may be a mechanism for these patients to cope with the high burden of treatment-and disease-related side effects. Our data also showed that patients who were currently undergoing active cancer treatment were more likely to decrease exercise. This may be confounded since patients who are currently undergoing treatment or recently completed treatment are likely to experience treatment-related side effects, impairments from surgical intervention, and may be more prone to infections due to weakened immune system and may want to avoid outdoor activities.

Patients following other healthy lifestyle behaviors such as never drinking alcohol or decreasing alcohol consumption during the pandemic were more likely to exercise more, which is consistent with previous studies (47) . Individuals who fall into an overall 'healthier' lifestyle cluster considering smoking, nutrition, alcohol, and physical activity, are generally more active (47) . Overall, our data suggest that the pandemic contributed to the factors that have been previously identi ed as barriers to exercise, resulting in less exercise during the pandemic among a signi cant proportion of cancer patients and survivors.

Strong evidence supports exercise as a coping mechanism for side effects of cancer, its treatment, and related behavioral health challenges including anxiety, depression, fatigue, and sleep di culties (48-50).

Research also shows that individuals with underlying mental health problems, perceived stress, or nancial hardship engage in less physical activity (51) (52) (53) . The pandemic has caused the majority of individuals to experience increased levels of stress and anxiety as well as nancial di culties due to loss of employment, income, or health insurance (8, 54). In addition, social distancing policies and other restrictions to prevent the spread of the virus have reduced the ability to cope with underlying mental health conditions. A recent study reported that individuals who remained active or increased their activity levels during the pandemic have done so to maintain their mental health (55) . In contrast, mental health conditions associated with the pandemic have emerged as barriers to exercise (55) . Our results con rm these ndings within the cancer population. In particular, patients who felt lonely, had less social interactions, were nancially stressed, and experienced perceived stress in terms of di culties piling up were more likely to exercise less and less likely to engage in more exercise. These results elucidate the need to screen for mental health challenges faced by cancer survivors during the pandemic and promote psychosocial programs that address unique needs and challenges within this population.

This study has several strengths and limitations. Exercise habits were self-reported and may be subject to recall bias. However, given the timeliness of the pandemic, the conscious perception of changes in life experienced by many, and prospective design of the study, we assume that patients can more easily recall any behavioral changes. Survey responses may have been biased by the type of survey (in person, phone, electronically). The majority of the study population was White, non-Hispanic/Latino, and from Utah.

Thus, the generalizability of our results may be limited and not applicable to those with different racial and ethnic backgrounds, or those from other states who may have had different COVID-19 state-wide policies. However, our study population included a signi cant proportion from rural residents (26%) making the results more applicable for other states with similar urban-rural proportions. The response rate was moderate and may have introduced selection bias.

The pandemic has impacted everyone's lives in many ways including changes in health behaviors. Health behaviors such as being physically active are even more important for immune compromised populations like cancer survivors. Our results indicate that many cancer patients and survivors reduced their exercise during the rst 6 months of the pandemic. This was more common among patients who had poor health, disruptions to daily life, reduced social interactions, and increased levels of psychosocial stressors such as loneliness and nancial stress. This study identi es risk factors for changes to physical activity among cancer patients and survivors as well as highlights targets for future interventions to prevent reduced physical activity and promote increased exercise.

Funding: This study was supported by the National Institutes of Health (NIH)/National Cancer Institute (NCI) grants (U01 CA206110, R01 CA211705, R01 CA189184, R01 CA207371, P30 CA042014 to C.M.

Ulrich) and the Huntsman Cancer Foundation. The sponsors had no role in the design or conducting of this research.

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Con icts of interest: Dr. Ulrich has as Executive Director of the Comprehensive Cancer Center at Huntsman Cancer Institute oversight over research funded by several pharmaceutical companies but has not received funding directly herself. Dr. Tward has served on an advisory board and consulted for Myriad Genetics, Inc., Decipher Biosciences, and Boston Scienti c; he has received research funding from Bayer for work outside of the present manuscript. Dr. Lee has served on advisory boards and/or consulted for Jazz Pharmaceuticals, Kite Pharma, Kadmon Corporation. Fresenius Kabi, and CareDx; she has received research funding from Incyte for work outside of the present manuscript. Dr. Gonzalez has served on advisory boards and/or consulted for SureMed Compliance, Elly Health, and KemPharm. Other authors declare that they have no con ict of interest.Availability of data and material: Data can be made available upon reasonable request.Code availability: Codes can be made available upon reasonable request.Ethics approval: The University of Utah Institutional Review Board (IRB) approved this protocol. Consent to participate: All participants provided written informed consent. Consent for publication: All authors provided consent to publish this manuscript.