Vol. 18 No. 4 (2024)

  • Open Access

    Article

    Article ID: 3839

    Perspectives and Challenges of Family Members in Providing Mental Support to Cancer Patients: A Qualitative Study in Beijing, China

    by Wei Wang, Lan Li

    Psycho-Oncologie, Vol.18, No.4, 2024; 41 Views

    This study explores the perspectives and challenges faced by family members providing mental support to cancer patients in Beijing, China. The primary objective is to understand the emotional and practical roles family members undertake and the difficulties they encounter. Utilizing a qualitative research design, data were collected through semi-structured interviews with family caregivers of cancer patients. Thematic analysis revealed several key themes: the dual burden of emotional support and caregiving responsibilities, the impact on daily life and personal well-being, the role and effectiveness of external support systems, perceptions of medical staff support, and the common challenges and conflicts faced in caregiving. The findings highlight the critical need for comprehensive support systems that address both the emotional and practical needs of family caregivers. Recommendations for enhancing family-centered support programs in oncology settings are discussed.

  • Open Access

    Article

    Article ID: 3840

    The Correlation between Psychological Resilience and Professional Quality of Life in Saudi Psychiatric Nurses: A Cross-Sectional Study

    by Ahmad M. Rayani

    Psycho-Oncologie, Vol.18, No.4, 2024; 26 Views

    In recent years, significant focus has been placed on resilience, with ongoing studies aiming to identify strategies for reducing the negative effects of job stress and protecting nurses from negative psychosocial outcomes. Nevertheless, as far as this topic is concerned, no research has yet been conducted in the context of Saudi psychiatric nurses. The aim of this research, therefore, is to determine how Saudi Arabian psychiatric nurses’ professional quality of life and psychological resilience relate to one another. To this aim, a cross-sectional study has been performed in Saudi Arabia incorporating a population of 167 (a 66.4% response rate) mental health nurses taken from the largest psychiatric hospital in the capital city Riyadh. Data collection was performed using the popular Arabic version of the Connor–Davidson Resilience and the Arabic version of the Professional Quality of Life Scales. To assess the variables related to both Professional Quality of Life and psychological resilience levels, statistical analyses such as Pearson correlation, ANOVA,  t -tests, and linear regression were utilized. The findings show compassion satisfaction and burnout to have a moderate inverse relationship (r = −0.502), while compassion satisfaction (CS) and resilience have a moderate positive correlation (r = 0.594). Compared to their morning-shift counterparts, nurses working night shifts reported higher mean scores for resilience (72.70), CS (40.20), burnout (24.52), and compassion fatigue (CF) (28.11). Participants with less than five years’ experience in a psychiatric clinic had the highest mean resilience score (72.96). Finally, a positive relationship between resilience and compassion satisfaction (CS) was revealed using linear regression analysis (β = 0.536,  t  = 7.080,  p  = 0.000). The study reveals significant differences in the scores assigned to resilience and work-life quality based on educational qualifications, shift-work type, and experiences. Burnout and compassion satisfaction (CS) are found to be significantly correlated, as are compassion satisfaction (CS) and resilience, and burnout and compassion fatigue (CF).

  • Open Access

    Article

    Article ID: 3842

    Advancement of Nursing Education in Psychosocial Oncology Care: Perspectives and Experiences of Nurses

    by Aida Sanad Alqarni, Fatmah Ahmed Alamoudi, Eddieson Pasay-an, Lizy Sonia Benjamin, Kawther Elthayeb Ahmed, Petelyne Pangket, Richard Maestrado, Lailani Sacgaca, Ferdinand Gonzales, Benito Areola Jr.

    Psycho-Oncologie, Vol.18, No.4, 2024; 13 Views

    Introduction:  The main objective of this study was to fill the gap between the knowledge nurses have about psychosocial care and what they do about cancer patients’ needs. It also aimed to devise ways to improve nursing education for nurses who could provide enhanced psychosocial support in such areas.  Methods:  This qualitative study relied on 18 in-depth interviews with nurses, with a focus on the difference between their understanding of psychosocial care and its application in helping cancer patients. This involved analyzing the transcribed interviews using thematic analysis. Data were collected from February to March 2024.  Results:  The verbal accounts of 18 participants were analyzed. These include theme 1 “holistic approach to cancer care” with the subtheme “navigating resource constraints:” theme 2 “nurses well-being and emotional input” with the subtheme “positive impact of psychosocial care:” theme 3 “Care for patients’ well-being” with subtheme “resourcefulness and resilience in psychosocial care:” theme 4 “adapting care and building connections:” theme 5 “ideal and reality in psychosocial care” with subtheme “challenges in delivering comprehensive cancer care:” and theme 6 “empowering nurses for effective psychosocial care” with subtheme “building a strong foundation for psychosocial care.”  Conclusion:  From the nurses’ perspective, this study indicates a need for more inclusive cancer treatment. Therefore, in addition to physical interventions, emotions and social welfare must also be addressed. Although emotionally invested, health workers may offer assistance along psychosocial lines, thus aiding both patients and caretakers. Although individualized care with personal connections is crucial for effective services, this approach can make it difficult to ensure that all clients receive adequate psychological assistance. Hence, there has been a call to enhance the training to produce nurses who offer high-quality services. This study emphasizes a more holistic approach toward the emotional needs of patients while supporting those responsible for them in their sickness journey.

  • Open Access

    Article

    Article ID: 3843

    The Impact of Nursing Staff’s Work Attitude on the Fear of Patients Recovering from Benign Tumors: Family Support as a Mediating Variable

    by Chengzhe Guo, Aihua Cheng, Jian Chen, Gaojie Cheng

    Psycho-Oncologie, Vol.18, No.4, 2024; 17 Views

    The perception of nursing staff’s attitude influences patient fear. Understanding this dynamic is crucial for fostering a supportive environment conducive to patient well-being and effective healthcare practices. The purpose of this research is to investigate how the attitudes and behaviours of nursing staff influence the fear and anxiety levels of patients recovering from benign tumors, aiming to improve patient care and recovery outcomes. Data was collected from a sample of 100 participants, comprising 20 nursing staff and 80 patients recovering from benign tumors. Surveys were administered to gather quantitative data on attitudes and fear levels. Participants were selected randomly from hospital records and outpatient clinics. Our analysis encompassed nursing staff attitude, patient fear levels, the influence of family support, progression of tumor recovery, patient-reported satisfaction, and the quality of healthcare services provided. The quantitative aspect utilized PLS-SEM software to perform regression analysis, evaluating both direct and indirect effects. Statistical analysis assessed the relationships between nursing staff attitudes, patient fear during benign tumor recovery, and the mediating role of family support. The findings of the study demonstrate that better nurse attitudes (Hypothesis 1, and stronger family support (Hypothesis 2, are linked to lower levels of patient fear. Partially mediating the relationship between nurse attitudes and patient fear, according to Hypothesis 3 , is family support. Patients’ perceptions of family support are highly influenced by nursing behaviour, as demonstrated by Hypothesis 4 . Our research showed a strong relationship between the attitudes of nursing personnel and patient fear levels. Family support demonstrated a strong mediating effect on patient fear. Patient-reported satisfaction is positively correlated with family support. However, no significant relationship was found between healthcare service quality and patient fear.

  • Open Access

    Article

    Article ID: 3845

    Employing a Backpropagation Neural Network for Predicting Fear of Cancer Recurrence among Non-Small Cell Lung Cancer Patients

    by Man Liu, Zhuoheng Lv, Hongjing Wang, Lu Liu

    Psycho-Oncologie, Vol.18, No.4, 2024; 17 Views

    Objective:  Non-small cell lung cancer (NSCLC) patients often experience significant fear of recurrence. To facilitate precise identification and appropriate management of this fear, this study aimed to compare the efficacy and accuracy of a Backpropagation Neural Network (BPNN) against logistic regression in modeling fear of cancer recurrence prediction.  Methods:  Data from 596 NSCLC patients, collected between September 2023 and December 2023 at the Cancer Hospital of the Chinese Academy of Medical Sciences, were analyzed. Nine clinically and statistically significant variables, identified via univariate logistic regression, were inputted into both BPNN and logistic regression models developed on a training set (N = 427) and validated on an independent set (N = 169). Model performances were assessed using Area Under the Receiver Operating Characteristic (ROC) Curve and Decision Curve Analysis (DCA) in both sets.  Results:  The BPNN model, incorporating nine selected variables, demonstrated superior performance over logistic regression in the training set (AUC = 0.842  vs . 0.711,  p  < 0.001) and validation set (0.7  vs . 0.675,  p  < 0.001).  Conclusion:  The BPNN model outperforms logistic regression in accurately predicting fear of cancer recurrence in NSCLC patients, offering an advanced approach for fear assessment.

  • Open Access

    Article

    Article ID: 3846

    Network Structure and Variability of Recurrence Fear in Early-Stage Non-Small Cell Lung Cancer: A Symptom Network Analysis

    by Lu Liu, Zhuoheng Lv, Yousheng Mao, Yan Liu, Man Liu

    Psycho-Oncologie, Vol.18, No.4, 2024; 13 Views

    Background:  Lung cancer, one of the most prevalent and deadly malignancies worldwide, not only poses a significant physical burden but also a profound psychological challenge to patients. Among these psychological challenges, the fear of recurrence stands out as a particularly distressing issue. This fear, often rooted in the patients’ past experiences with the disease and its treatment, can significantly impact their quality of life, mental health, and even compliance with follow-up care. Moreover, this fear can be exacerbated by the lack of understanding and support from healthcare professionals and family members, further isolating patients and compounding their psychological burden. Therefore, understanding and addressing the fear of recurrence in lung cancer patients is crucial for improving their overall well-being and outcomes.  Aims:  This study aims to develop a symptom network model for fear of recurrence in early-stage lung cancer patients, analyzing symptom correlations to enhance healthcare providers’ understanding and management of these symptoms, thereby improving patient outcomes and quality of life.  Design:  A cross-sectional study design was used.  Method:  We employed convenience sampling to recruit 551 lung cancer patients from the Thoracic Surgery Department of a tertiary hospital in Beijing between January 2023 and December 2023. A cross-sectional study was conducted using the General Information Questionnaire, Fear of Disease Progression Scale, and Level of Hope Scale. Network analysis was performed with JASP 0.18.3.0 using the EBICglasso method, and centrality metrics including Betweenness, Closeness, Degree centrality, and Expected influence were calculated.  Results:  Symptom network analysis identified fear of family impact and future work disruption as central to recurrence fear in these patients. Gender-based analysis revealed ‘fear of being unable to continue work’ as central in males, while ‘fear of affecting family members’ was central in females. Among adolescents, concerns about future work, medication side effects, and family impact showed the highest expected influence. In contrast, older patients predominantly feared major treatment implications. One-way ANOVA indicated that older age correlated with reduced recurrence fear, and higher hope levels significantly mitigated this fear.  Conclusion:  This study broadens understanding of fear of recurrence across demographic variables like gender and age, elucidating symptom interrelations and impacts. Future strategies should focus on patient-specific differences in recurrence fear to formulate targeted interventions.  Relevance to Clinical Practice:  Through in-depth analysis of the symptom network, healthcare professionals can more comprehensively understand the psychological responses of lung cancer patients when they face the risk of recurrence, and then formulate more precise and personalized treatment plans. At the same time, doctors and nurses can adjust treatment strategies in a timely manner according to the changes in the patient’s symptom network and provide more comprehensive psychological support, thus enhancing the patient’s treatment adherence and outcome.  Patient Contribution:  People who were invited to participate voluntarily completed a range of questionnaires.

  • Open Access

    Article

    Article ID: 3847

    Clinical Effect Observation of Constructing PERMA Model in Psychological Intervention for Patients with Chronic Cancer Pain

    by Yu-Feng Ren, Dong-Li Ji, Yu Wu, Ru-Qin Ben, Hai-Xia Wei

    Psycho-Oncologie, Vol.18, No.4, 2024; 8 Views

    Background:  The constructing PERMA model in psychological intervention was applied to patients with chronic cancer pain to provide data reference for reducing pain, fear of cancer recurrence, and improving the level of psychological capital.  Aim:  To explore the clinical effects of constructing PERMA model in psychological intervention for patients with chronic cancer pain.  Methods:  A total of 98 patients with chronic cancer pain admitted to our hospital from March 2021 to March 2023 were randomly divided into two groups, 49 cases in each group. The control group received routine intervention, while the research group constructed PERMA model based on the routine intervention for psychological intervention. The pain severity, fear of cancer recurrence, psychological capital and quality of life before and after intervention were compared between the two groups.  Results:  After two months of intervention, the pain in the research group was milder than that in the control group ( p  < 0.05). The scores and total scores of all dimensions of fear of cancer recurrence in the research group were lower than those in the control group ( p  < 0.05). The scores and total scores of each dimension of psychological capital in the research group were higher than those in the control group ( p  < 0.05). The scores of all dimensions of quality of life in the research group were higher than those in the control group ( p  < 0.05).  Conclusion:  The PERMA model constructed in psychological interventions for patients with chronic cancer pain can assist analgesic medications to reduce pain and alleviate the fear of cancer recurrence, increase the level of psychological capital, and thus improve quality of life.

  • Open Access

    Article

    Article ID: 3848

    L’impact du cancer de l’adolescent et du jeune adulte – AJA – sur le fonctionnement familial : étude des relations familiales en termes d’adaptabilité et de cohésion

    by Voskan Kirakosyan, Manon Arnoult

    Psycho-Oncologie, Vol.18, No.4, 2024; 12 Views

    Objectives:  The arrival of cancer in adolescents and young adults (aged 15 to 24 years)-Adolescents and young adults (AJA)- corresponds to a fragile period during which the adulthood of the young person and the evolution of family ties mobilize the family as a whole. Therefore, cancer, beyond its individual traumatic dimension, affects the whole family, which can modify family ties and family functioning. Our objective is to evaluate family functioning from the complex model evaluating cohesion and adaptability when an adolescent or young adult has cancer.  Methods:  Adolescents and young adults with cancer (n = 41), mothers (n = 41), and fathers (n = 13) participated in this study. They completed the Family Adaptation and Cohesion Scales (FACES III) questionnaire. Family functioning when an aya is ill has been compared to that of families without any disease.  Results:  a comparison of the mean scores of perceived cohesion and adaptability of face III indicates no significant difference for cohesion. In contrast, the averages of the adaptability scores of our sample with those of the general population indicate that families with cancer hais generally feel more “adaptable” than the non-clinical population. These results are statistically significant for AJA, but also for mothers and fathers. Regarding the mean scores of ideal cohesion and ideal adaptability, there are no significant differences between fathers in our sample and fathers in the general population. In contrast, mothers in our sample had less ideal adaptability than those in the general population. In aya patients with cancer, the scores of both adaptability and cohesion were significantly different from those of non-diseased adolescents.  Conclusion:  Cancer leads to many changes in family relationships, making it difficult to empower the young patient and latent the evolution of the relationship.

  • Open Access

    Article

    Article ID: 3849

    Influence des croyances et des représentations de la psyché dans l’après-cancer du sein

    by Virginie Di Silverio, Susann Heenen-Wolff, Jochem Willemsen, Patrick Derleyn

    Psycho-Oncologie, Vol.18, No.4, 2024; 16 Views

    For some, the announcement of a cancerous illness awakens or reinforces representations linked to the presumed power of the psyche over the body. Different psychosomatic theories underline the importance of a specific psychic functioning as the guarantor of good somatic health. In our view, confusion in the understanding of such concepts has effects on the aftermath for women with breast cancer. Our study was carried out by six women with breast cancer and focused on the influence of beliefs and representations of breast cancer on how they experienced the acute post-treatment phase of an oncology care pathway. We identify a possible link between beliefs and representations held by the patient, his or her family, and/or caregivers, and the possible reinforcement of defensive psychic movement we call “Transient Secondary Obsessional Movement” (TSOM). Longitudinal qualitative research using a combined approach involving non-directive clinical interviews and a projective test, the Szondi. A study focusing on two specific phases of the oncology care pathway: treatment (T1) and acute post-treatment (T2). An individual and cross-sectional analysis of the twelve Szondi protocols and a thematic analysis of non-directive clinical interviews were carried out. The results corroborate the identification of specific psychic movements for these six women. At T1, we observe a major need to cling, a psychic lability favoring the fixation of reassuring discourse and repression of effects. At T1 and T2, we identify a decathexis of the Ego and the presence of obsessional traits independent of the women’s psychic structure. At T2, there is a lifting of repression, a heightened sense of injustice, and a gradual new psychic cathexis. The psychic movement that takes place at T2 is the transition from the desire to “stay as before” (T1) to “I thought I’d go back to being as before”. The post-cancer period often reflects a dissonance between psychic time and medical time: an announced “healing” of breast cancer does not necessarily imply a psychic recovery for the women concerned. The TSOM represents a transitory psychic bridge, reflecting psychic vulnerability and after-effects. In a process of transition from the world of the sick to that of the healthy, each woman is seeking and/or attempting to control the uncertainty of the risk of the disease returning.

  • Open Access

    Article

    Article ID: 3850

    Oncosexology in côte d’Ivoire: Attitudes and Practices of Physicians Involved in the Management of Breast and Prostate Cancer

    by Kouamé Konan Yvon Kouassi, Bitti Adde Odo, Yenahaban Lazare Toure, Ouowene Prisca Marina Sougue, Petiori Gningayou Laurence épouse Kamara Touré, N’Guessan Manlan Prosper Mebiala, Fleur Audrey Sessegnon, Marie Sandrine Koff, Akissi Marie Barbara Yvonne Nogbou, Sherif Traore, Asmaho Akissi Danielle Andree Traore-Kouassi, Moctar Toure

    Psycho-Oncologie, Vol.18, No.4, 2024; 6 Views

    Objective:  To evaluate the attitudes and practices of oncosexology in the management of breast and prostate cancer in Côte d’Ivoire.  Methods:  A cross-sectional, multicenter, descriptive and analytical survey carried out over 02 months from 1 November to 31 December 2022, among doctors involved in the management of breast and prostate cancer in Côte d’Ivoire.  Results:  78 physicians on 114 participated in the study, with a participation rate of 79.5%. Only one doctor discussed the sexual risks associated with cancer with all his patients and 7.7% of doctors said they never broached questions of sexuality with their patients. The approach to sexuality was strongly associated with occupation ( p  = 0.002). A request for onco-sexological care was initiated by the patient and the partner respectively in 3.8% and 25.6% of cases. Only 5.1% of physicians claimed to have received training in oncosexuality. In 92.3% of cases, doctors would like to have training on this topic.  Conclusion:  On the questions relating to sexuality, Physicians are not addressing sexuality with their patients diagnosed with breast or prostate cancer. The lack of training in this area appears to be the main reason for this lack of communication and onco-sexological care.

  • Open Access

    Article

    Article ID: 3851

    Evaluation d’une stratégie multimodale d’information et de recueil des directives anticipées dans un Centre de Lutte Contre le Cancer : description du protocole de l’étude

    by Léonor Fasse, François Blot

    Psycho-Oncologie, Vol.18, No.4, 2024; 5 Views

    Background:  Information on the possibility of drawing up Advance Directives (AD) is a necessity, and represents a major medical, ethical, and legal challenge. The difficulties are numerous, both organizational and cultural, and this is also true in the context of oncology, where ADs (and more broadly, advanced palliative care) are of critical importance. As an eminently sensitive subject, dealing with ADs (and therefore with end-of-life issues) requires both societal and medical/health-care acculturation. An institutional approach has therefore been developed, to deploy information tools, training professionals, and formalize the collection of AD. Such an approach cannot be implemented without an assessment not only of its objective results but also above all of its psychological effects, on both users (patients, family caregivers) and professionals.  Methods:  This longitudinal study, based on a mixed-method, interdisciplinary approach, will assess the impact of this information dissemination on AD, in terms of both potential positive and negative effects, using validated measurement methods. Thus, this study follows the 5 criteria of the RE-AIM model, designed to analyze the interest and impact of a device intended for users of the healthcare system; we will use a mixed methodology, relying on both a quantitative component (counting the number of people benefiting from the scheme, and those requesting support in drawing up their DA..., administering questionnaires), as well as a qualitative component (focus groups) which will enable us to study the subjective experiences of users, their relatives and the professionals involved in the scheme.  Results:  The results of this study will make it possible to determine the effects of this system of assistance in the drafting of ADs, which is currently being promoted by the legislator, but which is struggling to be implemented.

  • Open Access

    Review

    Article ID: 3838

    Progress in Research on the Impact of Religious Psychological Coping on the Holistic Well-Being of Cancer Patients and Relevant Factors

    by Jing Li, Minghui Li, Guanghuan Xie

    Psycho-Oncologie, Vol.18, No.4, 2024; 25 Views

    This study reviews the historical development, current applications, and multifaceted impacts of religious psychological coping on the physical and mental health of cancer patients. As a method for coping with life’s pressures through religious beliefs or activities, religious psychological coping has been proven to alleviate the negative emotions of cancer patients and enhance their spiritual well-being and quality of life (QOL). Research indicates that religious faith can alleviate the physical symptoms of cancer patients, extend survival time, reduce the fear of death, assist in coping with treatment side effects, and improve self-efficacy and overall quality of life. Additionally, this study explores factors influencing religious psychological coping, including demographic and sociological characteristics, the faith status of caregivers, types of religion, the relationship between the course of the disease and the duration of belief, and psychological factors. Considering the cultural differences between China and other countries, this study calls for further research into the real experiences of cancer patients with religious beliefs and provides theoretical guidance for clinical nursing practices to achieve holistic care for the body, mind, and spirit of cancer patients.