Advances in Public Health

Advances in Public Health / 2020 / Article

Research Article | Open Access

Volume 2020 |Article ID 4817932 | 11 pages |

Challenges, Coping Strategies, and Social Support among Breast Cancer Patients in Ghana

Academic Editor: Carol J. Burns
Received19 Jun 2019
Revised10 Jan 2020
Accepted21 Jan 2020
Published25 Feb 2020


Background. Despite the high incidence and mortality rate of breast cancer (BC) in Ghana, little attention has been given to the issue of how adult women cope with having BC. The aim of this study was to explore the challenges, coping strategies, and support systems among women diagnosed with BC in Ghana. Methods. A descriptive cross-sectional study was conducted from February to August 2017 at the Komfo Anokye Teaching Hospital (KATH), Ghana. A systematic random sampling technique was used to select 202 women with a confirmed diagnosis of BC. Coping strategies of women with BC were assessed using the Brief-COPE. The associations between sociodemographic characteristics, social network/support, and coping strategies were assessed using linear regression models. Results. The most and least adopted active coping strategies were religious coping and humors, respectively. Self-distraction and substance use were the most and least adopted avoidant coping strategies, respectively. Spouses and children offered the most support to women with BC; having support from 5 or more sources was associated with higher mean active coping (beta [β] 1.14; 95% CI 0.66 to 1.62) and avoidant coping (β 1.46; 95% CI 0.98 to 1.94), as compared with having <2 sources of social support. Conclusion. This study demonstrates that women diagnosed with BC in Ghana adopt varied coping strategies to deal with these challenges. The forms of coping strategies adopted by women diagnosed with BC are influenced by the extent of social support received. Psychosocial counseling and support should be an integral part of BC management. Exploring and including social networks could play an important role in the management of BC in Ghana.

1. Background

Globally, breast cancer (BC) remains the second leading cause of mortality among women, with increasing rates particularly in developing countries where the majority of cases are diagnosed in late stages [1]. In Africa, it is the most commonly diagnosed cancer annually, with an estimated incidence of 168,690 cases and 74,072 related deaths in 2018 [2, 3]. In Western Africa, although precise estimates are lacking as a result of absence of a cancer registry in most countries, recent GLOBOCAN data estimate age-standardized incidence and mortality rates of 37.3 and 17.8 per 100,000 female, respectively, in 2018 [2, 3], making it the most commonly diagnosed cancer in women, a shift from previous decades in which cervical cancer was the most commonly diagnosed cancer [4]. Survival from BC is known to be markedly lower in Africa compared with other regions in the world [5]. This is not different in Ghana where BC has become the leading cause of mortality among women and it is also the common cause of hospital admissions among Ghanaian women [3, 6].

Breast cancer diagnosis along with its treatment can contribute to physical, social, and psychological turmoil. These challenges extend to the periods of posttreatment and recovery. The psychosocial challenge in BC patients is related to the essence of the breasts in a woman’s body image or femininity, sexuality, and motherhood [7]. Additional concerns include physical appearance and disfigurement after treatment, uncertainty regarding recurrence in the future, periods of anxiety and depression, difficulty maintaining hope, fear of death, as well as loss of self-esteem [8] for the patients and their loved ones, particularly life partners [9, 10]. Challenges also include the shock of a cancer diagnosis and fears about the future or the side effects of treatment, such as nausea and fatigue [11]. Practical aspects of treatment such as the cost and travel also pose challenges [11]. Although relatively rare, BC presents with even more challenges in younger women, who tend to have a more aggressive biology and an associated poorer diagnosis [12]. A study conducted among BC patients in Ghana reported a high prevalence of depression (84.2%) and anxiety (92.5%), with 44% having both and with the prevalence being significantly higher among those living without partners [13]. Experiences of emotional reactions such as sadness, fear, severe pain leading to suicidal ideations, and loss of hope have also been reported among Ghanaian women diagnosed with BC [14].

Women diagnosed with BC develop coping strategies to deal with the multifactorial unpleasant experience of a psychological, social, and spiritual nature of their new life situation [15]. Coping is defined as current cognitive and/or behavioral efforts adopted to deal with specific external and/or internal stresses or anxieties that are valued as challenges and beyond the control and resources of the person [16]. Effective coping strategies are indispensable for adaptation and adjustment to BC and improvement in survival [17, 18]. Coping strategies assist patients to deal with the problem that is causing the distress (problem-focused coping) and/or regulating stressful emotions (emotion-focused coping) [19, 20]. In Ghana, accepting the disease and surrendering to God has been reported as a coping strategy among women living with advanced BC [14]. The effectiveness of the coping strategy, however, depends on the degree of distress, variations in individual coping, the level of social support available and, to a large extent, the consultation skills and support of health professionals [21]. A link between social support and coping skills has been previously reported [22]. Early identification of coping strategies adopted by women with BC as well as patients who are coping poorly is important for treatment compliance, control of distress, and patient care in general.

Effective social support for BC patients could help reduce the negative impact of diagnosis and treatment and promote their psychological well-being [23, 24]. The social networks include friends, family members, healthcare professionals, and neighbors, and forms of support are mainly instrumental, structural and functional, emotional, and informational [11]. Health workers play an important role in orienting patients prior to treatment to help them choose the most suitable methods, thereby minimizing the level of stress and uncertainty [25]. In a study among young women diagnosed with BC, an increase in social support (measured by amount of social contacts) was associated with increased likelihood of survival [22]. Women living with BC in Ghana are known to receive some form of support from their families, spouses, friends, health professionals, and spiritual leaders [14].

Despite the high incidence-mortality rate of BC in Ghana, and the related psychosocial challenges, less attention has been given to the issue of how patients cope with their condition.

1.1. Theoretical Framework

The theoretical framework for this study consists of perspectives on coping and social support previously applied in breast cancer research as reflected in Lazarus’ [26] theory of appraisal, stress, and coping. According to Lazarus and Folkman [27, 28], coping involves persistently changing cognitive and behavioral efforts in order to manage specific external and/or internal demands that are seen as taxing or exceeding one’s resources. The stress associated with a situation depends on an individual’s appraisal of the situation and the behaviors directed at managing the stress. Lazarus [26] identified two major types of coping strategies. (i) Problem-focused coping lifestyle, which aims at solving the problem or situations, and (ii) Emotion-focused/avoidant coping lifestyle, aimed at regulating the emotions related to stress. Problem-focused coping includes obtaining relevant information about what to do, whereas emotion-focused includes avoiding to think about the threat or reappraising it without changing the realities of stressful situations. The two coping strategies can both facilitate and impede each other throughout a stressful situation.

The concept of social support has been defined and operationalized in different ways and is identified as important in adjusting to breast cancer [29]. It is a multidimensional concept that is generally theorized from a quantitative-structural perspective of social networks, such as numbers of persons and formal relationships with them, or from a qualitative-functional perspective of social support, such as the perceived content and availability of relationships with significant others [30]. The qualitative-functional support relates to the quality or function served by the structural support components and is mainly divided into the provision of instrumental, emotional, and informational support [31]. This study dwells on the buffer theory, which reflects the belief that support buffers against the adverse effects of stressors under conditions of high stress. The “buffering” effect of social support during stressful times with breast cancer has been previously investigated [32]. These studies generally conclude that social support from family and friends is associated with a better adjustment to BC.

The aim of this study was to explore the challenges, coping strategies, and support systems reported by women diagnosed with BC in the Kumasi metropolis, Ghana, and to assess the associations among sociodemographic characteristics, social support, and coping strategies.

2. Methods

2.1. Study Design and Setting

The study was a descriptive cross-sectional design and was conducted at the oncology unit of Komfo Anokye Teaching Hospital (KATH), Kumasi, from February to August 2017. KATH is the second largest hospital in Ghana and the only tertiary health institution in the Ashanti Region. The oncology unit, which is part of the clinical directorate of the hospital, was opened in 2004.

2.2. Study Population and Sampling

The study population included women with a confirmed diagnosis of BC at the oncology unit of Komfo Anokye Teaching Hospital and was willing to participate in the study. The sample size was estimated using Cochran’s sample size formula [33]: , where n0 = sample size for a population; t = standard normal deviation = 1.96; p = the estimated proportion of an attribute that is present in the population (assumed to be 15%); q = 1 − p (85%); and d = degree of accuracy, set at 5% and a confident interval of 95%, giving a total sample, n, of 196. 202 participants were finally included.

A pilot study was carried out first to establish the validity and reliability of the instruments and to assess the respondents’ ability to accurately understand questions asked. The researchers were trained to ensure consistency in the administration of the questionnaire including the translation of the questions to the local language for participants. The questionnaire was administered by the researchers to all those selected for the study.

The study participants were recruited using a systematic random sampling technique. Prior to data collection, we estimated the average respondents needed per day using the estimated number of days for data collection and the average patients’ attendance at the facility per day. We then estimated the sampling interval, K, using the average patients attendance and the average respondents needed per day (K = average patient attendance/needed respondents per day). On each day, during the visit hours, a first participant was identified and interviewed as the starting point, followed by the Kth respondent. This was repeated until the required sample size for each day was attained. We included women, 18 years and above, who had confirmed BC diagnosis at KATH and consented to participate in the study.

2.3. Assessment of Coping Strategies and Challenges

Coping strategies of women with BC were assessed using the Brief-COPE, which comprises 14 items, measuring two coping styles [34]. This instrument has been used to assess both habitual and dispositional coping (how people react in general), and more specific coping (how people react in relation to a specified stressful encounter). The Brief-COPE is a well validated scale that has been used extensively to assess coping strategies for many conditions including cancer [35] and depression [36].

The 14 items of the Brief-Cope measure self-distraction, active coping, denial, substance use, use of emotional support, use of instrumental support, behavioral disengagement, venting, positive reframing, planning, humor, acceptance, religion, and self-blame. The 14 items were grouped into two factors: adaptive/active coping (active coping, emotional support, positive reframing, planning, acceptance, religion, humor, and instrumental support) and maladaptive/avoidant subscale (venting, self-distraction, denial, substance use, behavioral engagement, and self-blaming) following Meyer [37]. The responses were on a Likert scale of four (4), directed at teasing out the frequency with which the women engaged in each strategy: 1 (I have not been doing this at all), 2 (I have been doing this a little bit), 3 (I have been doing this a medium amount), and 4 (I have been doing that a lot).

Challenges experienced were assessed on a Likert scale of five responses: 1 (never), 2 (rarely), 3 (sometimes), 4 (often), and 5 (always). There was a total of 10 items to measure possible challenges faced by women, including physical symptoms such as fatigue, fear of recurrence, body image disruption, sexual dysfunction, depression, and anxiety. The reliability statistics were mean 32.74; variance 67.75; standard deviation (SD) 8.23, and Cronbach’s Alpha 0.86.

2.4. Other Variables

Sociodemographic characteristics and social support were assessed using a structured questionnaire. The sources of social support assessed were spouses, children, parents, religious bodies, friends, physician or caregivers, and support groups. This was developed with recourse to other studies [38]. Using a Likert scale of five (5)—1 (strongly disagree), 2 (disagree), 3 (neutral), 4 (agree), and 5 (strongly agree)—responses indicated the level of agreement to whether support is received from any of these sources. The reliability statistics for this scale were mean 23.91; SD 7.05, and Cronbach’s Alpha 0.78. The form of support received from these sources was also assessed by responding “Yes” or “No” to each of the support systems. The forms of support assessed were financial, escort, emotional, and psychological counseling. Psychological support in this study meant psychological counseling to help the women deal with emotional and mental issues, whereas emotional support has to do with the receiving genuine concern and empathy from another person. The sources of social support were used as a proxy for the social network. This ranged from 1 to 8, based on the 8 sources of social support described above. The social network was further grouped into ≤2, 2–5, and ≥5 and used in the regression analysis to assess the influence of social networks on coping strategies.

The socioeconomic characteristics assessed were age, level of education (categorized as no education, primary, Junior High School, Senior High School, and Tertiary), marital status (categorized as single, married and living with partner, married and not living with partner, divorced/widowed), religion (Christians, Muslims, and traditionalists or other religion), number of children, employment status, and type of occupation.

2.5. Statistical Analysis

All statistical analyses were carried out using SPSS, version 22 [39]. General characteristics are summarized as proportions and mean (SD) or median (25th and 75th percentiles) based on the distribution of the variables. The influence of sociodemographic characteristics and social network/support on coping strategies was assessed using linear regression models. Two models were fitted; model 1 to control for the sociodemographic characteristics, while model 2 adjusted for both the sociodemographic characteristics and social networks. Two-tailed significance tests were used throughout, and was considered statistically significant.

2.6. Ethical Considerations

An ethical approval and registration certificate was obtained from KATH to carry out the study. All study protocols were reviewed and approved by the Institutional Review Board of the Kwame Nkrumah University of Science and Technology—Committee for Human Research Publications and Ethics (CHRPE). Research procedures were explained, and informed consent was received from all participants.

3. Results

3.1. Sociodemographic Characteristics of Study Respondents

The mean age (SD) of the women was 55 years (13.4), and age ranged from 33 to 87 years; 27.2% of the women had no formal education, while 17.8% had tertiary education. Majority of the women were married, of which 39.6% were living with their partners. The majority (68.8%) were Christians. The median (25th, 75th percentile) number of children was 3 (2, 5), and 10.4% had no children. The majority (68.8%) were employed with 40.3% being traders (Table 1).

N = 202

Age, mean ± SD55 ± 13.4
 No formal5527.2
 Primary school5426.7
 Junior high or middle school3617.8
 Senior high or secondary school2110.4
Marital status
 Married and living with partner8039.6
 Married and not living with partner4019.8
 No religion/traditional21.0
Number of children, median (25th, 75th percentile)3 (2, 5)
 7 or more188.9
Employment status
Types of occupation (n = 139)
 Civil or public servant2014.4
 Health professional117.9

SD, standard deviation.
3.2. Experience of Challenges

The mean responses indicate that most of the women sometimes experienced physical symptoms such as fatigue, trouble with sleeping, pain, and burnout, mean, sexual dysfunction, threat to their safety, and felt vulnerable. Most of the women often had intrusive thoughts about their illness and hence were depressed and anxious. Some women also had communication issues with their partners and body image disruptions (Table 2).


Physical symptoms such as fatigue, trouble sleeping, or pain, weight gain, burnout3.351.01Sometimes
Fear of recurrence3.731.20Often
Feelings of vulnerability3.211.14Sometimes
Body image disruption3.361.33Sometimes
Intrusive thoughts about illness3.681.09Often
Marital/partner communication issues2.581.41Sometimes
Sexual dysfunction2.711.41Sometimes
Experience of threats to safety3.221.21Sometimes
Reduced sexual interest and decreased sexual function.2.801.39Sometimes
Depression and anxiety3.951.15Often

SR, summary response; SD, standard deviation. Responses: 1 = never; 2 = rarely; 3 = sometimes; 4 = often; 5 = always. Challenges faced by women diagnosed with breast cancer measured using a questionnaire of 10 items, that is, possible challenges faced.
3.3. Support Systems for Women Diagnosed with Breast Cancer

The highest form of support was from religious bodies, churches, and the community (mean = 4.01) followed by children (mean = 3.67). The least form of support was from support groups (mean = 2.26) (Figure 1). We further aggregated the sources of social support and used as a proxy for the social network. The results indicate that approximately half (51%) of the women had support from five (5) sources or more, whereas 11.4% had support from two (2) sources or fewer. 10.9%, 8.9%, and 11.9% had support from six (6), seven (7), and eight (8) sources, respectively.

The forms of support received by the women were financial, escort, emotional, and psychological or counseling (Figure 2). The most form of support offered by spouses or children was financial (78.7%) followed by the escort (62.4%). The most form of support offered by religious groups was emotional support (57.4%). Psychological support or counseling was also provided mostly by physicians and care providers (74.8%). On the average, majority, 57% of the women had only one form of support, whereas 31%, 7.7%, and 4.2% had two, three, and four forms of support, respectively.

3.4. Coping Strategies

Majority of women frequently engaged in active coping strategies. The most adopted active coping strategy was religious coping, while the least adopted was humor. Self-distraction and substance use were the most and least adopted avoidant coping strategies, respectively (Table 3).


Active/problem focus (adaptive) coping strategies
 Active coping5.840.92
 Emotional support6.030.91
 Positive reframing5.180.90
 Religious coping6.970.78
 Instrumental support5.890.89
 Overall mean5.551.06
Avoidant/emotional focused (maladaptive) coping strategies
 Substance use3.230.88
 Behavioral disengagement4.480.93
 Overall mean4.561.06

aComputed by summing the means of two items/questions for each cooping variables. SD, standard deviation. Responses: 1 = I have not been doing this at all; 2 = I’ve been doing this a little bit; 3 = I’ve been doing this a medium amount; 4 = I’ve been doing this a lot. Coping strategies of women with BC were assessed using the Brief-COPE, which comprises 14 items, measuring two coping styles [34].
3.5. Factors Influencing Coping Strategies

Age, marital status, and employment status were associated with coping strategies adopted by women with BC. Higher age has no influence on active coping but might be associated with less avoidant coping (only shown in model 1). Being married was also associated with higher active coping in model 1 but not with avoidant coping. Being employed had a positive association with both active and avoidant coping strategies, although effect on avoidant coping was only observed in model 1. In the adjusted model, being employed was associated with 0.38 increase in mean active coping, as compared with those not employed (β 0.38; 95% CI 0.06, 0.70). Support by more than 2 persons increases both active and avoidant coping. Women who had more than 5 sources of support had 1.41 (β 1.14; 95% CI 0.66, 1.62) and 1.46 (β 1.46; 95% CI 0.98, 1.94) higher mean active and avoidant coping, respectively, compared with those who had support from <2 sources. Similarly, higher mean active and avoidant coping was observed for women with 2 to 5 sources of social support compared with those with <2 sources (Table 4).

β (95% CI)
Active copingCrude
β (95% CI)
Avoidant coping
Adjusted β (95% CI)Adjusted β (95% CI)
Model 1Model 2Model 1Model 2

Sociodemographic characteristics
Age−0.01 (−0.02, −0.003)a−0.07 (−0.02, 0.01)−0.01 (−0.02, 0.01)−0.02 (−0.03, −0.01)b−0.02 (−0.03, −0.01)c−0.01(−0.02, 0.01)
Education (ref = no education)
 Basic education−0.10 (−0.44, 0.25)−0.34 (−0.68, 0.00)−0.26 (−0.58, 0.07)0.24 (−0.12, 0.60)0.03 (−0.33, 0.38)0.16 (−0.17, 0.49)
 Secondary or tertiary education0.02 (−0.36, 0.40)−0.25 (−0.64, 0.14)−0.20 (−0.57, 0.18)0.14 (−0.26, 0.57)−0.15 (−0.36, 0.25)−0.10 (−0.48, 0.27)
Christian religion (ref = Islamic or other)0.06 (−0.25, 0.37)−0.09 (−0.39, 0.21)−0.08 (−0.37, 0.21)−0.09 (−0.41, 0.23)−0.24 (−0.56, 0.07)−0.22 (−0.50, 0.07)
Married (ref = single)0.48 (0.02, 0.80)c0.41 (0.02, 0.70)b0.19 (−0.10, 0.48)0.39 (0.10, 0.68)b0.24 (−0.06, 0.54)−0.05 (−0.34, 0.24)
Employed (ref = unemployed)0.60 (0.31, 0.90)c0.49 (0.17, 0.70)c0.38 (0.06, 0.70)a0.64 (0.33, 0.94)c0.48 (0.14, 0.81)b0.28 (−0.04, 0.60)
Social network (ref = <2)
2–50.80 (0.38, 1.22)c0.73 (0.30, 1.16)b0.80 (0.38, 1.22)c0.74 (0.31, 1.17)b
≥51.41 (0.96, 1.85)c1.14 (0.66, 1.62)c1.61 (1.16, 2.01)c1.46 (0.98, 1.94)c

a, bc; CI, confidence interval; ref, referent. Model 1 = adjusted model of sociodemographic characteristics; Model 2 = adjusted model of sociodemographic characteristics + social network. All analyses are exploratory.

4. Discussion

The women often had unpleasant thoughts about their illness, including fear of recurrence of the disease and were anxious and depressed. Sometimes, the women felt vulnerable and had sexual dysfunction, physical symptoms such as fatigue, burnout, and trouble with sleeping, and partner communication issues. We also found that coping strategies were associated with the extent of social network or support as well as the employment status of women diagnosed with BC.

Our findings corroborates those in Ghana that found a high prevalence of depression and anxiety [13] and experiences of sadness, fear, and severe pain leading to suicidal ideas among women living with BC [14]. This is also consistent to the reports from women elsewhere who expressed fear and anxiety and harbored fears of the recurrence of the disease [40] and disruption of body image [41]. Understanding these challenges and the nature of anxieties in cancer patient populations is important as abnormal anxiety affects the psychological well-being of the patients [42].

These intrusive thoughts, fear, and anxiety are partly related to the perceived stigma associated with BC diagnosis, especially in these settings. Cancer stigma is present in many communities, and it is a feared outcome of a cancer diagnosis, thereby militating against screening, early diagnosis, and treatment seeking for women with symptoms [43]. Losing one breast as a result of surgery, for instance, could lead to stigma and loss of self-esteem, resulting in distress and pain [44]. In Ghana, stigmatization and cultural barriers are important elements in the fight against BC. BC is largely seen as a spiritual disease, as a curse on a family (especially those with positive family history), caused by witchcraft, and as an incurable disease. This perception is similar among both urban and rural Ghanaian women [45, 46]. These perceptions, beliefs, and traditions impact on disease management and health-seeking behavior in relation to BC [43]. It is important to assist these women to adjust to these changes and adopt strategies to cope and deal with their current situation.

Although sexual dysfunction is well acknowledged as a major challenge among women diagnosed with BC, this was least reported in this study. Receiving a BC diagnosis and undergoing associated treatments including long-term therapy can impair sexual function via a number of mechanisms, including disrupting ovarian function, body image, intimacy, and relationships [47], contributing to a lower quality of life in BC survivorship. The low prevalence of sexually related challenges in this study could be due to underreporting. A population-based study among Ghanaian women reported an overall prevalence of 45.6% of female sexual dysfunction (FSD) [48]. High levels of environmental sexual reproductive health stigma among young women in Ghana have also been reported [49]. Majority of respondents in this study may also not be exposed to the various clinical factors such as hormonal alterations induced by chemotherapy and radiotherapy or physiological and functional disturbances related to the deterioration of physical condition. They might also be resilient to other psychological factors that induce disturbances in sexual behavior such as anxious/depressive reactions in adapting to the illness and treatment, hypochondriacal and cancer phobic reactions, regressive tendencies, and loss of self-esteem [50].

In an attempt to deal with their health and psychosocial issues relating to the diagnosis of BC, these women adopt various coping strategies. We found a high frequency of use of active coping strategies among the women studied. These strategies are adaptive, favorable, and problem-focused, and individuals accept and actively attempt to deal with their situation. The women in this study engaged frequently in positive reframing, planning, acceptance, and religious coping. This corroborates previous findings, which identified religion, acceptance, planning, active coping, and positive reframing as various active coping strategies among women diagnosed with BC in Iran [22]. These strategies have been shown to have a positive influence on the women’s adjustment to BC, by influencing positively the psychological well-being and health behaviors of these patients [51].

Religion was the most frequently used active coping strategy in this study. This corroborates previous findings in Ghana that suggested that women diagnosed with advanced BC surrendered to God and prayed for the will of God to prevail regarding their conditions [14]. Findings from other settings also found a religious approach and spiritual fighting as key active coping strategies among newly diagnosed cancer patients [52]. These studies suggest that a relationship with God provides a consistent and reliable source of support and comfort as well as support from a religious community, especially among people of African descent [53]. In Ghana, women demonstrate their will to live by praying positively and being hopeful for long life despite their predicament [14]. In a study conducted in the United Kingdom, a majority of the BC patients used positive religious coping to some degree at surgery [54]. Participating in religious service ignites a sense of belonging among these women and buffers against feelings of isolation [55].

This study also assessed avoidant coping strategies among women. These strategies are problem focused and include strategies such as denial, behavioral disengagement, and alcohol/drug. We found that venting or voicing, self-distraction, and behavioral disengagement were frequently used avoidant coping strategies, whereas humor, substance use, and self-blaming were less frequently used. It is important to assess how these strategies influence health outcomes among this group of patients. The influence of coping on psychological well-being depends on the situation and characteristics of the individual [56]. Avoidant coping would have less of a negative association with patients’ mental and physical well-being when patient symptoms were low and vice versa [57].

Social support networks have been shown to be significantly important in helping people manage life crises and health challenges [58]. The sources of support endorsed in this study were spouses, children, parents, religious bodies or community, friends and health providers, with children being the most cited. Similarly, a study conducted in Ghana found that BC patients received support from their families, spouses, friends, health professionals, and spiritual leaders [14]. Spouses, children, families, and friends were dominant in providing forms of support to these women. This corroborates findings from previous studies, which showed that spouses and families were supportive, giving confidence, listening to the patients, and supporting them in the decision-making process about the treatment [59, 60]. A recent systematic review also found emotional support by spouses, family members, and friends as the main forms of support for women with BC [61]. Religious bodies provided emotional support, psychological counseling, and some form of financial assistance, whereas physicians and care providers provided counseling and emotional support to these women. Arora et al. [60] also found that most women diagnosed with BC receive helpful informational and emotional support from healthcare providers. These supports are important for the psychological well-being of the patients especially in the early stages of diagnosis, where patients face the greatest anxiety [62], and the absence of it could hamper effective healthcare access by BC patients [63]. Support from support groups was less in this study compared with other sources of support. It is important to assess the formats of these support groups, costs involved in attending to these groups as well as the contents of these groups and how these influences assess, and provision of support to BC patients in Ghana.

We found an association between support systems and coping strategies among women diagnosed with BC. Women with more sources of social support were more likely to adopt a coping strategy as compared with those with fewer sources of social support. Being employed, and therefore having more social contact, was also positively associated with active coping strategy among the women studied. This corroborates previous evidence, which shows that an increase in social support increases women’s survival by enhancing their coping skills, providing emotional support, and expanding opportunities for information sharing [64]. Women with BC who are in support groups have significantly better psychological well-being, more posttraumatic growth, better self-image, better sexual functioning and higher sexual satisfaction, better coping and communication, and fewer physical symptoms associated with BC [65]. A meta-analysis of existing literature on interventions delivered to family caregivers of cancer patients also showed a significant, positive effect on multiple health outcomes [66].

Contrary to previous findings, social support was positively associated with avoidant coping strategies in this study, indicating that although social support encourages women to adopt active coping strategies, some women still resort to avoidant coping despite having support socially. This is supported by Lazarus and Rice [56] notion that avoidant coping strategies are not always maladaptive and might have differential effects depending on the degree of symptom and distress a patient is experiencing [56]. We also believe that the avoidant coping lifestyles are rooted in stigmatization and negative perceptions, which could not be demystified regardless of their support from their social networks. We recommend further studies into stigmatization, psychosocial challenges, and how these influence strategies with breast cancer. It is also important to further explore support systems available to these women at all levels and how they relate to survival outcomes and quality of life.

4.1. Clinical Implications

Findings from this study show various challenges associated with BC diagnosis in Ghana and point to the need for healthcare professionals to elicit these challenges and support the women with psychosocial support. This study further shows the need to elicit the coping strategies adopted among women diagnosed with BC and help identify women who require special counseling and support. Psychological screening is recommended for women diagnosed with breast cancer during their treatment period. Such screening can support healthcare professionals with information and better understanding of the psychosocial needs of breast cancer patients and the coping skills required to meet those needs.

4.2. Limitations

The instruments used to measure coping in this study had not been previously validated in this setting although they were pretested to ensure their reliability in this study population. Being a cross-sectional analysis, causation cannot be concluded. Previous studies have however identified social support as an important factor in managing challenges associated with BC diagnosis. This study also did not collect information on the clinical characteristics of the patients, including the stage of the disease and the kinds of treatment received by the patients in this study.

5. Conclusion

In conclusion, this study demonstrated varied challenges faced by women diagnosed with BC in Ghana, including fear and anxiety and intrusive thoughts about their illness. These women also most frequently used various active coping strategies, especially religious coping in dealing with their health and psychosocial issues. Women diagnosed with BC explore and receive various forms of support, and their extent of social support and social networks influences their coping with challenges associated with their ailment. It is important to ascertain the level of social support and further explore and create opportunities to involve family members in breast care management.


BC:Breast cancer
KATH:Komfo Anokye Teaching Hospital
KNUST:Kwame Nkrumah University of Science and Technology
SPSS:Statistical Package for Social Sciences
CHRPE:Committee for Human Research Publications and Ethics
SD:Standard deviation.

Data Availability

Data for this study are securely kept by the principal investigator and will be made available upon request.

Conflicts of Interest

The authors have no funding or conflicts of interest to disclose.


The authors are grateful to the staff and management of the Oncology Department of the Komfo Anokye Teaching Hospital, Ghana, for their assistance in this study and to all participants who took part in the study.


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Copyright © 2020 Ruth Boatemaa Benson et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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