Sleep Quality, Cancer-Related Fatigue, and Health-Related Quality of Life Among Omanis Hospitalized Patients with Cancer: A Cross-Sectional Study.

DOI: https://doi.org/10.21203/rs.3.rs-274232/v1

Abstract

Purpose: This study aimed to examine the difference in HRQoL by participants’ characteristics and to investigate the determinants of health-related quality of life HRQoL among Omani hospitalized patients with cancer.

Methods: This cross-sectional study was conducted in two oncology centers in Oman. Omani hospitalized patients with breast, thyroid, colorectal, stomach, and prostate cancer were recruited using convenience sampling. Participants completed Arabic versions of self-reported questionnaires: Pittsburgh Sleep Quality Index, Brief Fatigue Inventory scales and Functional Assessment of Cancer Therapy. Descriptive and inferential statistics were performed. T-test, ANOVA and multiple linear regression analysis was utilized to determine predictors of HRQOL.

Results: in total, 275 participants were recruited (Meanage= 52 years). About 64 % of the participates reported poor sleep and 18.5% reported severe cancer-related fatigue. Sleep quality, cancer-related fatigue, age, and prostate and thyroid cancer were significant predictors of HRQoL (F (5, 269) = 26.26, p < 0.000) and they explained 33% of the variances in the HRQoL (R2 = .328).

Conclusions: This study highlights the impact of sleep quality and caner-related fatigue on the HRQOL among Omanis hospitalized with cancer. Thus, sleep quality and cancer-related fatigue should be assessed routinely during hospitalization of oncology patients with special attention patients’ age.  

Introduction

Globally, over the past century, there has been a dramatic increase in cancer incidence and mortality, making it the second leading cause of death after cardiovascular disease [1]. Cancer mortality expanded by 25% from 1990, with an anticipated frequency of 23.6 million cases annually by 2030 [2]. The global cancer burden estimated to have risen to 18.1 million new cases and 9.6 million deaths in 2018 [3]. Cancer has been reported that one in six women and one in five men will develop cancer during their lifespan [4]. In the Eastern Mediterranean region (including the Middle East), about 555,318 cancer cases were reported in 2012 [5]. The number of cancer cases is estimated to double in nearly 20 years, meaning that the Eastern Mediterranean is expected to rank the highest relative increase in the world [5]. In Oman, 30% of the mortality rate is attributed to neoplasm; the crude cancer incidence rate among Omanis was 63.91 per 100,000 for men and 74.88 per 100,000 for women [6]. Furthermore, for solid cancer, breast cancer is the most common type of cancer among Omani female (24.48%), followed by thyroid (15.47%) and colorectal (7.51 %). Among Omani males, prostate cancer was the most common solid type (11.08%), followed by colorectal (10.95%), and stomach (6.00%) [6].

Universally, cancer burden and its management have been linked to consequences such as financial burden, increased morbidity, impaired quality of life, and premature death [7]. Cancer impacts on patients' physiological, psychological, and social status have been the subject of concern lately [8]. Sleep quality and cancer-related fatigue are two significant physical consequences experienced by adult patients with cancer affecting their quality of life and disabling daily functioning, memory, and concentration [8]. Health-related quality of life (HRQoL) is commonly used to observe the influence of health status on the general quality of life and is used as a primary outcome measure in studies evaluating the success and effectiveness of cancer treatment [9]. Poor sleep quality is known to be a dominant concern in about 60% of patients with cancer [10] with a potential effect on patients' HRQoL, which has been coupled with a decrease in functional performance and psychological status of patients with cancer [11]. Like poor sleep quality, severe cancer- related fatigue is commonly found among 25% to 99% of patients with cancer [12]. Cancer-related fatigue is a common side-effect of cancer and its treatment that is regarded as a risk factor leading to a reduction in cancer survival and HRQoL [12] and treatment suspension [13].

Similar to other Middle Eastern countries, patients' characteristics, sleep quality, and cancer-related fatigue and their influence on HRQoL among patients with cancer have not received adequate attention in Oman. The aims of this study were to examine 1) difference in HRQoL by participants’' demographical and clinical characteristics, sleep quality, and cancer-related fatigue, and 2) determinants of HRQoL among hospitalized Omani patients with cancer.

Methods

A descriptive correlational cross-sectional was carried out in two oncology centers in Oman, which are considered the country's main oncology centers that provide management to all patients with cancer. The study was conducted from June to October 2019.

We used a non-probability convenience sampling to recruit patients with cancer. The sample size was determined based on the numbers of independent variables included in multivariate regression analysis, which was recommended to be 10-20 participants per variable [14]. As a rule of thumb, we counted 15 participants per variable (total of 18 variables). Accordingly, the required sample size was 270 participants. The total participants included in the study were 275.

Participants were included if they were: Omani aged ≥ 18 years, hospitalized, diagnosed with cancer (i.e., breast, thyroid, colorectal, stomach, prostate cancer), aware of cancer diagnosis, understand and read Arabic, and willing to participate in the study. Participants who were critically ill, unable to complete the survey, and had cognitive impairment were excluded from the study.

Participants admitted in the oncology, and surgical units were screened for eligibility using a patient list obtained through electronic medical records. Eligible participants were initially contacted by the principal investigator (PI) to inform them about the study purpose and got an informed written consent form. Voluntary participation and refusal to participate would not affect their treatment was assured. Participants self-completed the questionnaire. The clinical data were obtained through medical records by the PI. Data were collected from two main oncology centers, representing 11 governorates of Oman, from June to October 2019. Permission to use all questionnaires described hereinafter was obtained from the primary developer. The study was approved by the Ethics and Research Committees of both centers: Sultan Qaboos University and Ministry of Health (CON/EA/26/2019, SRC#46/2019), respectively. The study was performed in line with the principles of the declaration of Helsinki.

All participants completed the Pittsburgh Sleep Quality Index (PSQI), the Brief Fatigue Inventory (BFI), and Functional Assessment of Cancer Therapy (FACT-G) questionnaires. In this study, sleep quality was assessed by the Pittsburgh Sleep Quality Index (PSQI) [15]. PSQI is a self-report measure with evidence of good internal homogeneity, test-retest reliability, validity, sensitivity (89.6%), specificity (86.5%), and Cronbach's alpha of 0.83 [15]. The PSQI distinguishes "poor" from "good" sleep that has been used in the cancer population widely [16] and the Arab cancer population, specifically [17]. PSQI is rated on a 0-3 Likert-like scale, whereby 0 (no difficulty) to 3 (severe difficulty). In a clinical cancer population, a cutoff score of ≥ 8 suggests a poor sleep, while a score of ≤ 7 indicates a good sleep quality [15, 18]. The PSQI Arabic translated version showed internal consistency of 0.74 in the Arabic cancer population [19]. In the current study, Cronbach's alpha of PSQI was 0.63, and we categorized sleep as poor quality (score ≤ 7) or good quality (score ≥ 8).

Cancer-related fatigue was assessed using the Brief Fatigue Inventory scale (BFI), a reliable tool established for the rapid assessment of fatigue severity in clinical screening for patients with cancer [20]. The scale's items are rated numerically from 0 to 10 and consists of nine items; the first three assess fatigue severity (0= No fatigue and 10= as poor as you can imagine for the first 3 items), while the remaining six items assess fatigue interference with general activity, mood, walking, work, relation and enjoyment (0= Does do not interfere, 10= completely interfere). The BFI psychometric evaluation supports its internal consistency and constructs validity with Cronbach's alpha of 0.96 [20]. BFI scoring is categorized into two groups: 1) severe fatigue (score of 7-10) and 2) non-severe fatigue (score of 0-6) with a higher score indicating higher fatigue severity. In the present study, fatigue was categorized as non-severe (score of 0-6) and severe (score of 7-10). The Arabic translated version BFI showed good internal consistency and convergent validity with a Cronbach alpha of 0.86 [18]. In the present study, BFI Cronbach's alpha was 0.89.

Health-related quality of life (HRQoL) was measured by using version 4 of the FACT-G that was developed by David Cella and to be used in the oncology population [21]. FACT-G has been administered in several types of cancer, validated with reliability Cronbach's alpha of 0.88, and translated into different languages [22]. FACT-G includes four domains: physical, social and family, emotional, and functional [21]. FACT-G version 4 has 27 items; each answered using a 5-point Likert Scale ranging from 0 (Not at all) to 4 (Very much). Total scale and subscale scores are summed to yield 108 points, with the higher scores indicating better HRQoL [22]. The current study showed a Cronbach's alpha of the FACT-G of 0.84 for the total score.

Data analyses

Statistical Package for the Social Sciences (SPSS) Version 24 was used for data entry and analysis. In this study, data were tested for normality by using Histogram, Plots, Skewness, and Kurtosis where all data were normally distributed. For the study variables description, continuous variables presented with mean and standard deviation, while categorical variables were presented with frequencies and percentages. The categorical association was compared by using the Chi-square test, and continuous association was compared by using the T-test, Pearson correlation, and One-Way Analysis of Variance (ANOVA). To examined the determinants of HRQoL, a multiple linear regression analysis was used. Multiple linear regression assumptions (i.e., normal distribution, linearity, and multicollinearity) were examined and not violated.

Results

Sample demographical and clinical characteristics

A total of 275 participants were included in this study, with a mean age of 52 years (SD= 14.1). The majority were female (65.1%), had chronic diseases (56%), and had a family history of cancer (37%). The mean total score of FACT-G was 73.0 (SD= 16.2) above the midpoint of 54. Among HRQoL domains, the social and family well-being scored the highest mean (Mean= 21.1, SD= 5.3), and physical well-being scored the lowest mean (Mean=15.6, SD= 17.0). The majority of participants had breast cancer (41.1%), were at stage IV (45.1%), and in the first year of cancer diagnosis (70%). Out of 275 participants, 64.4% were anemic and on chemotherapy (43.3%). The majority (64.4%) reported poor sleep quality, and 18.5% reported non-severe cancer-related fatigue (Table 1).

Health-related quality of life by patient’s demographical and clinical characteristics, sleep quality, and cancer-related fatigue

We used Pearson correlation, t-test, and ANOVA analysis to examine the difference in HRQoL by patients’ characteristics, sleep quality, and cancer-related fatigue. The findings showed that age was significantly and positively related to HRQoL (r = 0.25, p<0.001) reflecting as age increased, HRQoL is getting better. In regard to demographical variables, HRQoL varied significantly by level of education [F (3,271) = 12.26, p = 0.000], family history of cancer [t (273) = 2.29, p= 0.017] and income [F (3,271) =8.56, p= 0.000]. In regard to clinical variables, HRQoL varied significantly by type of cancer [F (4,270) = 7.34, p= <0.001], stage of cancer [F (3,271) = 9.55, p= 0.000], chemotherapy status [F (2,272) = 7.84, p= 0.000], and anemia status [t (275) = 3.91, p <0.001]. HRQoL was also significantly affected by sleep quality [t (273) = -7.90, p = 0.00], and cancer-related fatigue [t (273) = -5.54p = 0.000] (Table 2).

Determinants of health-related quality of life

A multiple linear regression model was used to examine the determinants of HRQoL. Variables that influenced HRQoL significantly (i.e., income, educational status, age, family history of cancer, chronic disease, sleep quality, cancer-related fatigue, cancer stage, cancer type, years of disease diagnosis, anemia status, and chemotherapy status; table 2) were only entered into the regression model. The multiple linear regression model showed that age, sleep quality, cancer-related fatigue, and cancer type were significant determinants of HRQoL. The model was significant, (F (5, 269) = 26.26, p < 0.000) and it had explained 33% of the variance in HRQoL (R2 = .328). The model showed that HRQoL is worse in patients with advanced age (B = -0.266, p= 0.000) and patients who had poor sleep quality (B = -11.387, p= 0.000) and severe cancer-related fatigue (B = -6.639, p= 0.003). Furthermore, the model indicated that HRQoL is significantly better in patients with prostate and thyroid cancer (B =8.466, p= 0.001; B = 6.225, p= 0.047), respectively. (Table 3).

Discussion

This study was conducted in Oman. It included 275 participants diagnosed with breast, thyroid, colorectal, stomach, or prostate cancer. The main aim of the study was to examine the determinants of HRQoL in hospitalized patients with cancer in Oman and to investigate if HRQoL varied by patients' demographical and clinical variables, cancer-related fatigue, and sleep quality. Findings of the study showed that HRQoL differed significantly by patients’ demographical and clinical characteristics, sleep quality, and cancer-related fatigue. Furthermore, results showed that age, poor sleep quality, severe cancer-related fatigue, and being diagnosed with thyroid or prostate cancer were significant determinants of HRQoL.

Our findings showed that 64% of Omani patients with cancer reported poor sleep quality, which is similar to a Lebanon study that showed poor sleep quality was high among patients who had non-metastatic breast cancer during active treatment [17]. It is also consistent with findings of a systematic review that reported about 30-70% of newly diagnosed patients with breast, thyroid, colorectal, stomach, and prostate cancer had poor sleep quality [23]. Various factors suggested the growth of poor sleep quality among patients with cancer, of which, cancer treatments modalities, the frequent awakening of patients in midnight and early morning for a nursing procedure or therapy administration, breath discomfort, hospital environmental noise, pain, and worries about illness and treatment are some examples influencing sleeping patterns [17]. In Oman, these factors could also explain why the majority of patients reported poor sleep quality taking into consideration that about 82% of patients were receiving chemotherapy. This study established baseline data about sleep quality in patients with cancer in Oman. Our finding highlights that health care professionals should pay attention to patients’ sleep patterns and quality and identify specific factors that can be managed to improve patients’ sleep quality and, subsequently, improve their health-related quality of life.

The mean total score of HRQoL was 73.0 (SD=16.2), which was above the midpoint of 54. Physical well-being, which involves issues related to pain, nausea, low energy, feeling ill, treatment's side effects, and trouble meeting family's needs, showed the lowest score among HRQoL domains, and physical well-being seemed to pose the most significant challenge for patients with cancer in Oman. A similar result was found in Saudi Arabia, a middle eastern Arabic country, for patients with solid cancer [24]. A Low physical well-being score could be related to the fact that the majority of the Omani patients included in this study were in stage III and IV, were anemic, and had poor sleep quality, all of which have been found to influence the overall HRQoL in current study significantly. Additionally, in this study, social and family well-being domains (feeling like being close to friends, family and friend's support, family cancer acceptance, feeling close and getting enough support and love from the partner) were reported the highest score compared to the other three domains. This finding is parallel to a previous Omani study among oncology population that found Omani patients said that their relationships with husbands and family members became more substantial and more supportive after diagnosis with cancer [25], which could explain our findings considering that 73.8% of patients were married. This finding also supports the notion that social support can improve distress and alleviate coping skills among Omani women challenged with cancer and its management [26]. This finding denotes that healthcare providers should improve patients' physical well-being and correlate this domain to patients’ sleep quality.

In this study, we found that poor sleep quality, severe cancer-related fatigue, age, and type of cancer (prostate and thyroid) significantly determine HRQoL and explained about 33% of the variance in HRQoL. This study had found that those participants with poor sleep quality had decreased HRQoL in general. This finding is in line with the literature that showed sleep quality as one of the main predictors of HRQoL; for instance, Ha and colleague (2019) reported that sleep quality was an important determinant of HRQoL in patients with lung cancer; and that poor sleep quality, dyspnea, fatigue and depression were related to lower HRQoL, and together accounted for 85% of variances in HRQoL [27]. Likewise, a Nigerian study among women with breast cancer with lower sleep quality showed a significant reduction in HRQoL [28]. In the Arab world, a study in Palestine reported that sleep quality was one of the HRQoL determinants and, together with the pain, were responsible for 42% of the variance in HRQoL [29]. The positive and significant relationship between poor sleep quality and low HRQoL could be related to the negative impact of poor sleep on the patients' immune systems, making them more susceptible to infection and illness [30]. Another explanation could be linked to the fact that poor sleep tempts changes in the cognitive performance of the patients with cancer, which, as a result, influence their HRQoL [31]. Besides, Poor sleep quality is connected with poor physical well-being, such as gastrointestinal dysfunction that aggravates sickness [32]. The current study extends the observations of the relationship between sleep quality and HRQoL from Western societies to the developing world, specifically the Arabs Omani population, and enlightens future focus to promote screening for and improving sleep quality to enhance HRQoL community with cancer.

 Likewise, cancer-related fatigue was found as another determinant of HRQoL in Oman, in which those with severe fatigue had a significant reduction in their overall HRQoL. Our finding is similar to studies from Nigeria, Greek, and France that were conducted in patients with breast and colorectal cancer and found that cancer-related fatigue was a significant determinant of HRQoL [28, 33, 34]. In the Arab population, we couldn’t identify literature examining the relationship between fatigue and HRQoL. Many reasons could explain the relationship between fatigue and HRQoL; one reason could be attributed to chemotherapy management and its side-effects [35], and this could explain our finding as about 43% of our participants were on chemotherapy. Other reasons could be due to the effect of cancer-related fatigue on patients’ self-care behavior as they demonstrated less involvement in taking care of themselves, which as a result, affect their HRQoL [36]. Although cancer-related fatigue experienced by the participants in the current study was as low as 18.5%, nevertheless, cancer-related fatigue remains a disabling symptom, a common determinant of patients' HRQoL, and it may prolong to two years after diagnosis [33, 34]. These findings could inform the future direction to establish strategies to understand cancer-related fatigue and its attributing factors to enhance HRQoL of patients with cancer.

In this study, age was also found to determine HRQoL in the Omani oncology population, indicating that HRQoL is better among younger age. Our findings were similar to results among cancer population from Sweden and Turkey [37, 38], but inconsistent with a study in Yemen, an Arab Country, that reported no relationship [39]. This finding could be because as people get older, they demonstrated lower performance in activities of daily living, lower functional abilities, and more risk of depression, which in consequence, reduce the HRQoL and supporting our finding [37, 40]. Our finding underlines the mounting need to focus HRQoL at a younger age and pay specific attention toward senior patients. In the Omani context of Oman and based on our findings related to the mean age of our participants (52 years), special attention toward improving HRQoL among older patients with cancer should be accentuated. 

Thyroid and prostate cancer found to determine HRQoL in hospitalized Omani, and that those with thyroid and prostate cancer reported better HRQoL compared to other types of cancer. Our findings were similar to a study from Iran [41] but inconsistent with studies from Turkey and France who reported no association [42, 43]. The high survival rate of prostate and thyroid cancer compared to another type of cancer could explain the link between these types of cancer and HRQoL compared to other cancer such as stomach (70%) and colorectal (80%) [44].

This study should be considered within the following limitation; first, use of a cross-sectional design limits the ability to establish causal relationships. Second, we use a convenient nonprobability sample, which could impede the generalizability of the findings. However, a heterogeneous sample from the largest two tertiary health settings in Oman could minimize this threat. Third, Pittsburgh Sleep Quality Index (PSQI) instrument had below the satisfactory level of internal reliability (Cronbach's alpha = .67), which is similar to another recent Omani study that used PSQI among myocardial infarction patients that reported a Cronbach's α of 0.64 [45]. However, having an adequate sample size could provide robust statistical power and confidence in the results.

Sleep quality, cancer-related fatigue, and HRQoL deserve adequate medical attention regarding supportive care and routine assessment. Prompt recognition, observation, and documentation of these variables will guide the clinical teams to develop interventions to improve fatigue and sleep quality and their impact on the health-related quality of life. Holistic multidisciplinary cancer care is necessary to implement by clinicians inside the hospital and out of the hospital to improve all aspects of HRQoL of oncology population. On the other hand, an individualized approach should be maintained considering unique patients’ characteristics such as age, cancer type, stage, and treatment modalities. Policymakers should design the oncology centers to empower patients’ physical, functional, social, and emotional well-being. Sleep quality, cancer-related fatigue, and HRQoL can be regarded as quality indicators for patients with cancer. Finally, future studies should examine 1) strategies to improve sleep quality and cancer-related fatigue across the cancer population in general and the Arab community in specific, 2) the same variables among patients with non-solid cancer like leukemia and 3) determinants of each subscale as this was not the scope of the current study.

Conclusion

Health-related quality of life is a multidimensional construct that necessitates further understanding. Sleep quality, cancer-related fatigue, and patients' clinical and demographical characteristics could impose critical determination of overall HRQoL.

Declarations

Funding

No funding was received for conducting this study

Conflicts of interests

The author(s) declared no potential conflict of interest with respect to the research, authorship, and/or publication of this article.

Ethics approval

The study was approved by the Ethics and Research Committees of both centers: Sultan Qaboos University and Ministry of Health (CON/EA/26/2019, SRC#46/2019), respectively. The study was performed in line with the principles of the declaration of Helsinki and was reported based on STROBE reporting guidelines for cross-sectional studies.

Consent to participate

Written informed consent was obtained for each participant according to national and institutional guidelines.

Consent to Publish

NA

Data Availability

The data set used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors’ contribution

All authors contributed to the study conception and design. Material preparation, data collection and analysis were performed by Zamzam Al-Habsi. The first draft of the manuscript was written by Zamzam Al-Habsi, and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.

References

  1. World Health Organization (2020) cancer Today. http://gco.iarc.fr/today/home
  2. Hamadeh, R. R., Borgan, S. M., & Sibai AM (2017) Cancer Research in the Arab World: A review of publications from seven countries between 2000-2013. , . Sultan Qaboos Univ Med J 2:147–154. https://doi.org/10.18295/squmj.2016.17.02.003
  3. World Health Organization (2018) Latest global cancer data. Latest global cancer data
  4. American Cancer Society. (2017) Cancer facts and Figures 2017
  5. World Health Organization (2017) Early detection of cancers common in the Eastern Mediterranean Region
  6. Ministry of Health (2018) Oman Cancer Registry
  7. Fitzmaurice C, Dicker D, Pain A, et al (2015) The Global Burden of Cancer 2013. JAMA Oncol 1:505–527. https://doi.org/10.1001/jamaoncol.2015.0735
  8. Costa DSJ, Mercieca-Bebber R, Rutherford C, et al (2016) The Impact of Cancer on Psychological and Social Outcomes. Aust Psychol 51:89–99. https://doi.org/10.1111/ap.12165
  9. Yin S, Njai R, Barker L, et al (2016) Summarizing health-related quality of life (HRQOL): Development and testing of a one-factor model. Popul Health Metr 14:1–9. https://doi.org/10.1186/s12963-016-0091-3
  10. Mercadante S, Aielli F, Adile C, et al (2015) Sleep Disturbances in Patients with Advanced Cancer in Different Palliative Care Settings. J Pain Symptom Manage 25:1301–1306. https://doi.org/10.1016/j.jpainsymman.2015.06.018
  11. Chen D, Yin Z, Fang B (2018) Measurements and status of sleep quality in patients with cancers. Support Care Cancer 26:405–415. https://doi.org/10.1007/s00520-017-3927-x
  12. Bower JE (2014) Cancer-related fatigue--mechanisms, risk factors, and treatments. Nat Rev Clin Oncol 11:597–609. https://doi.org/10.1038/nrclinonc.2014.127
  13. Wang XS, Woodruff JF (2015) Cancer-related and treatment-related fatigue. Gynecol Oncol 136:446–452. https://doi.org/10.1016/j.ygyno.2014.10.013
  14. Bujang MA, Sa’at N, Sidik TMITAB (2017) Determination of minimum sample size requirement for multiple linear regression and analysis of covariance based on experimental and non-experimental studies. Epidemiol Biostat Public Heal. https://doi.org/10.2427/12117
  15. Buysse DJ, Reynolds CF, Monk TH, et al (1989) The Pittsburgh sleep quality index: A new instrument for psychiatric practice and research. Psychiatry Res 28:193–213. https://doi.org/10.1016/0165-1781(89)90047-4
  16. Akman T, Yavuzsen T, Sevgen Z, et al (2015) Evaluation of sleep disorders in cancer patients based on Pittsburgh Sleep Quality Index. Eur J Cancer Care (Engl) 24:553–559. https://doi.org/10.1111/ecc.12296
  17. Fakih, Rahal M, Hilal L, et al (2018) Prevalence and severity of sleep disturbances among patients with early breast cancer. Indian J Palliat Care 24:35–38. https://doi.org/10.4103/IJPC.IJPC_137_17
  18. Suleiman K, Al Kalaldeh M, AbuSharour L, et al (2019) Validation study of the Arabic version of the Brief Fatigue Inventory (BFI-A). East Mediterr Heal J 25:784–790. https://doi.org/10.26719/emhj.19.032
  19. Carpenter JS, Andrykowski MA (1998) Psychometric evaluation of the Pittsburgh Sleep Quality Index. J Psychosom Res 45:5–13. https://doi.org/10.1016/S0022-3999(97)00298-5
  20. Mendoza TR, Wang XS, Cleeland CS, et al (1999) The rapid assessment of fatigue severity in cancer patients: Use of the brief fatigue inventory. Cancer 85:1186–1196. https://doi.org/10.1002/(SICI)1097-0142(19990301)85:5<1186::AID-CNCR24>3.0.CO;2-N
  21. Cella BDF, Tulsky DS, Gray G, et al (1993) The Functional Assessment of Cancer Therapy scale: Development and Validation of the General Measure. Am Soc Clin Oncol 11:570–579
  22. Victorson D, Barocas J, Song J, Cella D (2008) Reliability across studies from the functional assessment of cancer therapy-general (FACT-G) and its subscales: A reliability generalization. Qual Life Res 17:1137–1146. https://doi.org/10.1007/s11136-008-9398-2
  23. Ancoli-Israel S (2015) Sleep Disturbances in Cancer: A Review. Korean Soc Sleep Med 6:45–49
  24. Ahmed AE, Almuzaini AS, Alsadhan MA, et al (2018) Health-Related Predictors of Quality of Life in Cancer Patients in Saudi Arabia. J Cancer Educ 33:1198–1203. https://doi.org/10.1007/s13187-017-1198-3
  25. Al-Azri M, Al-Awisi H, Al-Rasbi S, Al-Moundhri M (2014) Coping with a diagnosis of breast cancer among Omani women. J Health Psychol 19:836–846. https://doi.org/10.1177/1359105313479813
  26. Shams N, Al-azri M (2019) The Effect of Cognitive Behavior Stress Management Program on the Distress , Coping Skills , and the Social Support of Omani Women with Breast Cancer : A Pilot Study. Am Sci Res J Eng Technol Sci 55:170–187
  27. Ha D, Ries AL, Swigris JJ (2019) Determinants of Cancer-specific Quality of Life in Veteran Lung Cancer Survivors Eligible for Long-Term Cure. In: bioRxiv
  28. Jaiyesimi AO, Sofela EA, Rufai AA (2007) Health related quality of life and its determinants in Nigerian breast cancer patients. Afr J Med Med Sci 36:259–265
  29. Dreidi MM, Hamdan-Mansour AM (2016) Pain, Sleep Disturbance, and Quality of Life Among Palestinian Patients Diagnosed with Cancer. J Cancer Educ 31:796–803. https://doi.org/10.1007/s13187-015-0946-5
  30. Besedovsky L, Lange T, Haack M (2019) The sleep-immune crosstalk in health and disease. Physiol Rev 99:1325–1380. https://doi.org/10.1152/physrev.00010.2018
  31. Alhola P, Polo-Kantola P (2007) Sleep deprivation: Impact on cognitive performance. Neuropsychiatr Dis Treat 3:553–567
  32. Zhao W, Jin H, Xu M, et al (2018) Sleep Quality of Functional Gastrointestinal Disorder Patients in Class-Three Hospitals: A Cross-Sectional Study in Tianjin, China. Biomed Res Int 2018:1–5. https://doi.org/10.1155/2018/3619748
  33. Faury S, Rullier E, Denost Q, Quintard B (2020) Quality of life and fatigue among colorectal cancer survivors according to stoma status - the national VICAN survey. J Psychosoc Oncol 38:89–102. https://doi.org/10.1080/07347332.2019.1638481
  34. Lavdaniti M, Owens D, Liamopoulou P, et al (2019) Factors Influencing Quality of Life in Breast Cancer Patients Six Months after the Completion of Chemotherapy. Diseases 7:26. https://doi.org/10.3390/diseases7010026
  35. Abu Obead K, Yaser S, Khattab M, et al (2014) Chemotherapy-induced fatigue among jordanian cancer patients: What are the contributing factors? Middle East J Cancer 5:75–82
  36. O’Regan P, McCarthy G, O’Reilly S, et al (2019) Cancer-related fatigue and self-care agency: A multicentre survey of patients receiving chemotherapy. J Clin Nurs 28:4424–4433. https://doi.org/10.1111/jocn.15026
  37. Klompstra L, Ekdahl AW, Krevers B, et al (2019) Factors related to health-related quality of life in older people with multimorbidity and high health care consumption over a two-year period. BMC Geriatr 19:187. https://doi.org/10.1186/s12877-019-1194-z
  38. Ogce F, Ozkan S, Baltalarli B (2007) Psychosocial stressors, social support and socio-demographic variables as determinants of quality of life of Turkish breast cancer patients. Asian Pacific J Cancer Prev 8:77–82
  39. Sawsan Ba-Khubaira WA-K (2012) Age related quality of life among selected breast cancer patients in Aden, Yemen. Pan Arab J Oncol 5:14–17
  40. Pergolotti M, Deal AM, Williams GR, et al (2017) Activities, function, and health-related quality of life (HRQOL) of older adults with cancer. J Geriatr Oncol 8:249–254. https://doi.org/10.1016/j.jgo.2017.02.009
  41. Heydarnejad MS, Hassanpour Dehkordi A, Solati Dehkordi K (2011) Factors affecting quality of life in cancer patients undergoing chemotherapy. Afr Health Sci 11:266–270
  42. Akin S, Guner CK (2017) Determinants of Fatigue , Self-efficacy , and Quality of Life of Cancer Patients During Chemotherapy : A Study from Turkey. J Nurs Sci 3:17–26
  43. Metallo M, Groza L, Brunaud L, et al (2016) Long-Term Quality of Life and Pregnancy Outcomes of Differentiated Thyroid Cancer Survivors Treated by Total Thyroidectomy and I131 during Adolescence and Young Adulthood. Int J Endocrinol. https://doi.org/10.1155/2016/7586482
  44. American Cancer Society (2020) Survival Rates for Prostate Cancer. https://www.cancer.org/cancer/prostate-cancer/detection-diagnosis-staging/survival-rates.html
  45. Almamari RS, Lazarus ER, Muliira JK (2019) Information needs of post myocardial infarction patients in Oman. Clin Epidemiol Glob Heal 7:629–633. https://doi.org/10.1016/j.cegh.2019.02.006

Tables

Table 1: Sample demographical and clinical characteristics and Health-related Quality of Life (n=275)

Characteristics

Mean (SD)

Age in years

52.1 (14.1)

Admission Days in the Hospital

 

Anemic Status

 

Anemic

177 (64.4)

Non-anemic

98 (35.6)

Total FACT-G

73.0 (16.2)

Physical well-being

15.6 (17.0)

Social/Family well-being

21.1 (5.3)

Emotional Well-being

18.0 (4.2)

Functional Well-being

18.3 (5.8)

Characteristics

n (%)

Gender

 

Male

96 (34.9)

Female

179 (56.1)

Level of Education

 

No education

83 (30.2)

Basic education

78 (28.4)

High school

69 (25.1)

University/College education

45 (16.1)

Occupation

 

Employed

98 (35.6)

Self-employed

3 (1.1)

Retired

43 (15.6)

Searching for job

2 (0.7)

Student

1 (0.4)

Social security

24 (8.7)

Housewife

104 (37.8)

Marital Status

 

Single

28 (10.2)

Married

203 (73.8)

Devoiced

10 (3.6)

Widow

34 (12.4)

Monthly income

 

≤ 300 OMR

137 (49.8)

301-700 OMR

56 (20.4)

701-1000 OMR

40 (14.5)

>1000 OMR

41 (14.9)

Presence of chronic disease

 

Yes

153 (55.6)

No

120 (43.6)

Family History of Cancer

 

Yes

102 (37.1)

No

171 (62.2)

Type of Cancer

 

Breast

113 (41.1)

Thyroid

23 (8.4)

Colorectal

68 (24.7)

Stomach

37 (13.5)

Prostate

34 (12.4)

Stage of Cancer

 

Stage I

6 (2.2)

Stage II

56 (20.4)

Stage III

89 (32.4)

Stage IV

124 (45.1)

Stage of Cancer

171 (62.2)

Years since Cancer Diagnosis

 

One year

192 (69.8)

Two year

52 (18.9)

Three year

17 (6.2)

Four year

14 (5.1)

Chemotherapy Status

 

Received

107 (38.9)

On Chemotherapy

119 (43.3)

Not Received

49 (17.8)

Surgical Status

 

Done

191(69.5)

Not done

84 (30.5)

Radiotherapy Status

 

Done

82 (29.8)

Not done

193 (70.2)

Immunotherapy Status

 

On immunotherapy

86 (31.3)

Received

27 (9.8)

Not for immunotherapy

162 (58.9)

Sleep Quality

 

   Poor sleep quality

177 (64.4)

  Good sleep quality

98 (35.6)

Cancer-related Fatigue

 

    Severe

51 (18.5)

    Non-severe

224 (81.5)

 SD= Standard deviation; OMR: Omani Riyals; FACT‐G: Functional Assessment of Cancer Therapy‐ questionnaire.

 Table 2: Health-related quality of life by patient's demographical and clinical variables

Variables

n

Mean (SD)

P-value

Age (r)

275

0.25 ‡

<0.001

Family history

Yes

No

 

104

171

 

75.90 (17.23)

71.31 (15.38)

 

0.03

Level of education

No formal education

Basic

Higher school

University/College

 

83

78

69

45

 

68.12 (16.06)

69.86 (15.77)

75.68 (16.36)

83.60 (11.03)

 

<0.001

Income

 ≤300

301-700

701 – 1000

> 1000

 

138

56

40

41

 

69.70 (16.18)

75.75 (17.13)

71.23 (14.10)

82.39 (12.95)

 

<0.001

Family history

 Yes

 No

 

104

171

 

75.90 (17.23)

71.31 (15.38)

 

0.03

Type of cancer

Breast

Thyroid

Colorectal

Stomach

Prostate

 

113

26

68

37

34

 

72.58 (17.89)

86.65 (11.34)

68.70 (14.22)

68.22 (14.55)

79.32 (11.71)

 

<0.001

Caner stage

Stage I

Stage II

Stage III

Stage IV

 

6

56

89

124

 

94.83 (12.32)

80.34 (15.01)

72.16 (16.58)

69.33 (14.87)

 

<0.001

Anemic status

Anemic

Non-anemic

 

113

162

 

77.50 (16.95)

69.93 (14.98)

 

<0.001

Sleep Quality

 Good sleep quality

 Poor sleep quality

 

98

177

 

83.55 (14.28)

69.29 (14.33)

 

0.000

Cancer-Related Fatigue

Non-Severe

Severe

 

224

51

 

76.81 (14.93)

63.65 (15.39)

 

0.000

 Table reflects significant values only, † Pearson Correlation, ‡ r value

 Table 3: Determinants of Health-Related Quality of Life†

Variable

B

SE(B)

Beta

t

p-value

95% CI

Poor Sleep Quality

-11.387

1.817

-0.337

- 6.265

0.000

-14.965 – -7.809

Age

-0.266

0.061

-0.232

- 4.356

0.000

-0.387 – -0.146

Prostate Cancer

8.466

2.540

0.172

3.334

0.001

3.466 –13.466

Severe CRF

-6.639

2.193

-0.159

- 3.027

0.003

-10.957– -2.321

Thyroid Cancer

6.225

3.123

0.106

1.994

0.047

0.077 – 12.373

R2 =0.328; CRF=Cancer-Related Fatigue.

This model used a stepwise elimination method. The model included variables: age, educational status, income, chronic disease, family history of cancer, cancer type, cancer stage, years of disease diagnosis, anemia status, chemotherapy status, sleep quality, and CRF.