Volume 30, Issue 4 (7-2020)                   JHNM 2020, 30(4): 217-223 | Back to browse issues page


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Toygar I, Usta Yeşilbalkan Ö, Kürkütlü M, Akgün T. The Relationship Between Social Support From Family and Quality of Life Among Cancer Patients: A Cross-Sectional Study. JHNM 2020; 30 (4) :217-223
URL: http://hnmj.gums.ac.ir/article-1-1474-en.html
1- Research Assistant Doctor, Department of Internal Medicine Nursing, Faculty of Nursing, Ege University, Izmir, Turkey. , ismail.toygar1@gmail.com
2- Professor Doctor, Department of Internal Medicine Nursing, Faculty of Nursing, Ege University, Izmir, Turkey.
3- Registered Nurse, Medical Park Hospital, Izmir, Turkey.
4- Registered Nurse, Tulay Aktas Oncology Hospital, Faculty of Medicine, Ege University, İzmir, Turkey.
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Introduction
Along with the development of health systems and treatment opportunities, the mortality rate of chronic diseases and cancer decreases, and life expectancy increases [1]. According to the American Cancer Society, while the cancer incidence has not significantly changed, cancer-related death decreases by 1.4% to 1.8% each year. Thus, the number of people living with cancer increases every year [2].
The Quality of Life (QoL) has gained importance in cancer patients, because of the increase in survival and life expectancy. The disease and side effects of treatments lead to the reduction of QoL in the patients. Nayak et al. reported that 82.3% of cancer patients had low QoL scores [3]. Moreover, the rate of patients with low QoL scores is higher regarding advanced cancer [4]. Numerous factors have been reported as the predictors of QoL; these factors include radiotherapy treatments, the feeling of loneliness, marital status, education status, comorbidity, and weight loss. Although the factors associated with the QoL of cancer patients are well-known, these patients still report the low levels of QoL [5]. 
Improving the QoL is considered one of the main objectives in the care of cancer patients [3]. Achieving this objective, the factors affecting the QoL should be determined. The effect of social support on the QoL of cancer patients has been extensively studied [6]. It was reported that perceived social support is associated with QoL in cancer patients. However, the effect of social support from family on the QoL has not been evaluated in cancer patients.
Social support positively affects the well-being of patients. These positive effects may help improve the QoL. Social support protects against the harmful effects of stressful events and helps people to cope with anxiety and depression. The lack of social support is reported as predictive of higher mortality. Besides, social support has a positive correlation with the health, functioning, psychological, spiritual, and family-related aspects of QoL. However, social support has a possible negative effect in that it could increase the patients’ dependency [7].
The term social support from family—as a type of social support—usually refers to the financial, social, and moral assistance that is provided to the stressed individual by the family members. The patients primarily receive support from the family in coping with difficulties. This support is important in providing and maintaining an individual’s physical and psychological well-being, thus, it may help improve the QoL [8]. However, a limited number of studies have examined the relationship between perceived social support from family and QoL. Therefore, the present study aimed to determine the relationship between perceived social support from family and the QoL in cancer patients.

Materials and Methods
It was a cross-sectional study that was conducted in the oncology services of a university hospital in İzmir City, Turkey, from March to October 2019. The study was conducted with overall cancer patients who had been diagnosed for more than 6 months. The inclusion criteria were over 18 years of age, the ability of Turkish communication, and the lack of cognitive disorder. A convenience sample of patients was obtained from patients meeting the inclusion criteria. Out of 728 patients who were admitted to the hospital during the study period, 593 met the inclusion criteria. However, the study was carried out with 276 voluntary participants.
The patient’s identification form was developed by the research team. The form consisted of 11 questions about age, gender, marital status, income level, education level, cancer-involved area, the duration of disease, family type, and the family history of cancer. 
The Quality of Life index-cancer version (QLI-C) was developed by Ferrans [9]. The QLI-C consists of two parts and measures the QoL of cancer patients, based on the patients’ satisfaction and the importance of the various aspects of life. Can et al. investigated the validity and reliability of the Turkish version of the QLI-C. The scale consists of 33 items and 4 sub-dimensions, including functional, family, social-economic, and psychological-spiritual. Scores are calculated for the overall QoL and each of the four domains. The satisfaction and importance scales are scored on a 6-point rating-type scale ranging from 1=very dissatisfied (very unimportant) to 6=very satisfied (very important). The total score ranges from 66 to 396, with a higher score representing better QoL [10]. The scale takes approximately 10 minutes to fill and no special training is required for its administration.
The Perceived Social Support from family scale (PSS-Family) was developed by Procidano and Heller [11]. Also, the PSS-Family is adapted into Turkish society [12]; thus, the scale is valid and reliable for Turkish society. The PSS-Family consists of one dimension and 20 questions that are answered as “yes”, “no”, or “I don’t know”. For each item, the perceived social support provided by family or friends was scored as +1 for “yes” and 0 for “no”, also, the “Don’t know” category was not scored. Thus, the scores range from 0 (indicating no perceived social support) to 20 (indicating maximum perceived social support). Higher scores indicate higher perceived social support from the family [12]. The scale takes approximately 5 minutes to fill and no special training is required for its administration.
The patient identification form, QLI-C, and PSS-Family were used to collect the research data. The data were collected by the same researcher in the study. The researcher asked the questions and filled the form in line with the patient’s response.
Data analysis was performed with IBM SPSS-25 for Windows (IBM Corp., Armonk, New York, USA). In this study, the continuous and categorical variables were expressed as mean±standard deviation and frequency (percentage), respectively. After the evaluation of the normal distribution of the data, a linear regression analysis was used to evaluate the relationship between PSS-Family and QLI-C.

Results
Most participants were female (65.2%) and married (73.6%). Also, 39.9% of the participants reported that they have a bachelor’s or higher degree of education. More than half of the participants (56.9%) reported that their incomes are equal to their expenses. Table 1 presents the distribution of the other disease-related characteristics of the study sample.

 

The Mean±SD scores of the PSS-Family and QLI-C were 16.43±3.01 and 307.77±27.48, respectively. Moreover, the Mean±SD scores of the functional, social-economic, psychological-spiritual, and family sub-dimensions were 128.95±14.58, 71.54±7.22, 75.03±7.48, and 32.33±4.24, respectively (Table 2).
 

Factors that affect both PSS-Family and QLI-C may affect the regression model. Thus, the statistical differences between sociodemographic and disease-related characteristics and the scales were evaluated to determine these factors. The PSS-Family and QLI-C did not significantly differ from gender, marital status, family history of cancer, age, the duration of disease, and family type. According to Table 3, the PSS-Family positively affects the QLI-C (P=0.001) and the subscales of the QLI-C.
 

Discussion
One of the main goals of care in cancer patients is to improve the QoL. Factors affecting the QoL should be known to plan effective interventions to improve the quality of life in cancer patients [3]. This study aimed to evaluate the effect of perceived social support from family on the QoL in cancer patients.
In the current study, the Mean±SD score of PSS-Family in cancer patients was 16.43±3.01. In the same society, Pehlivan et al. [13] reported the Mean±SD score of PSS-Family as 15.2±0.2. Also, Yıldırım and Kocabıyık [14] reported the Mean±SD score of PSS-Family as 15.92±3.22. Therefore, our study is similar to the literature in this respect. The family ties are reported as a strong and extended family structure, which is common in Turkish society. Thus, people living in Turkey spend more time in the family, compared with the people of many other countries [13, 14]. This difference may interpret these findings.
We found that the increase of social support from family positively affects the QoL in cancer patients. Each type of social support provides estimates for the overall QoL [15]. Eom et al. [16] reported that low social support is associated with poor QoL. According to the study of Zhou et al. [17], the overall social support contributes to the improving QoL in males who are undergoing prostate cancer treatment. Similarly, the results of our study explain the relationship between perceived social support from family and the QoL in cancer patients. Also, the current study is consistent with the literature of perceived social support from family. The literature reports include some beneficial effects of overall social support on the patients’ health [8]. We thought that social support from family involves the same beneficial effects. However, further studies are needed to explain the positive effect of perceived social support from family on QoL in cancer patients.
This study determined that the perceived social support from the family positively affects all the sub-dimensions of the QoL index, especially the family sub-dimension. In this regard, recent study report a relationship between functional status and social support [18]. Furthermore, Ozkan and Once [19] reported the positive effect of social support on the functional status in cancer patients. Besides, social support had a positive effect on psychological well-being [20]. Luszczynska et al. [21] reported that social support improves the emotional, functional, and physical QoL, among lung cancer patients. Thus, this aspect of our study is consistent with the literature.
According to the present results, the increase of social support improves the QoL through the positive effects on the overall well-being. This connection is also reported in the literature. No negative effect of social support from family was observed [22]. However, as a negative effect of social support, it was reported that the increase in social support increases the dependency of the patient [7]. The design and questionnaires of the current study were not suited to evaluate this effect of social support. Thus, further studies are recommended to determine this aspect of social support from family.
The increase in perceived social support from the family significantly improves the QoL in cancer patients. So, the perceived social support from the family should be considered while evaluating the QoL of cancer patients. While the interventions are planned to improve the QoL in cancer patients, interventions that increase perceived social support from the family should also be considered. We recommend further research on the subject.
The study has some limitations. it was conducted with the participants diagnosed with cancer, but there was no particular cancer group. Investigation with the separated cancer groups may provide new specific findings and solutions. As the participants were patients admitted to the hospital, the study is not necessarily generalizable. 

Ethical Considerations
Compliance with ethical guidelines

Written permission was obtained from the Medical Research Ethical Committee of the university (Protocol: 19-7T/62), hospital (54148036-100), and participants to conduct the study. All participants signed an informed consent form. Also, all principles of the Declaration of Helsinki were observed throughout the study.
Funding
This research did not receive any specific grant from funding agencies in the public, commercial, or non-profit sectors.
Authors' contributions
All authors equally contributed to all parts of the study.
Conflict of interest
The authors declared no conflict of interest.

Acknowledgements
We thank all patients for their collaboration and Su Özgür for statistical analysis.


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Article Type : Research | Subject: General
Received: 2020/09/29 | Accepted: 2020/07/30 | Published: 2020/07/30

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