Chiara Acquati

No Patients Left Behind: A Systematic Review of the Cultural Equivalence of Distress Screening Instruments

Despite the widespread use of distress screening instruments in cancer care, the reliability and validity of these instruments for a diverse population of cancer patients have not been well established. This is a systematic review of the conceptual and statistical equivalence of screening instruments of 148 psycho-oncology studies that included distress screening instruments. The findings indicate that screening measures of distress have comparable reliability, sensitivity, and specificity for White, Latino, and Asian samples. However, it is unclear if equivalent psychometrics are found among minority ethnic groups (e.g., African American) and immigrants within countries. Given the ethnic diversity among cancer patients and the lack of representation of this diversity in the current research, it is critical that researchers begin to include cancer patients of minority ethnic/racial groups in their samples so that health care providers can screen for distress with cultural sensitivity.

Coping with early stage breast cancer: Examining the influence of personality traits and interpersonal closeness

The study examines the influence of personality traits and close relationships on the coping style of women with breast cancer. A sample of 72 Italian patients receiving treatment for early stage breast cancer was recruited. Participants completed questionnaires measuring personality traits (Interpersonal Adaptation Questionnaire), interpersonal closeness (Inclusion of the Other in the Self Scale), and adjustment to cancer (Mini-Mental Adjustment to Cancer Scale). We hypothesized that diverse personality traits and degrees of closeness contribute to determine the coping styles shown by participants. Multiple regression analyses were conducted for each of the five coping styles (Helplessness/Hopelessness, Anxious Preoccupation, Avoidance, Fatalism, and Fighting Spirit) using personality traits and interpersonal closeness variables (Strength of Support Relations, and Number of Support Relations) as predictors. Women who rated high on assertiveness and social anxiety were more likely to utilize active coping strategies (Fighting Spirit). Perceived strength of relationships was predictive of using an active coping style while the number of supportive relationships did not correlate with any of the coping styles. Implications for assessment of breast cancer patients at risk for negative adaptation to the illness and the development of psychosocial interventions are discussed.

Sexual functioning among young adult cancer patients: A 2-year longitudinal study

Cancer‐related sexual dysfunction has been reported among adolescents and young adults (AYAs); however, its prevalence over time has not been examined. This longitudinal study investigated sexual dysfunction in AYAs over the course of 2 years after the initial diagnosis.

What Is Hope For Breast Cancer Patients? A Qualitative Study

This study explores the function of hope in the life experience of women diagnosed with breast cancer. Despite its relevance, hope is a psychosocial concept still not fully explored by the literature. Aim of the present contribution is therefore to conduct a qualitative examination of semi-structure interviews of women with breast cancer. In particular the connection between hope and eight domains (diagnosis, life events, supportive network, healthcare network, medical treatment, acceptance of the disease, ability to make projects and spirituality) associated with it is investigated. The analysis of the interviews of four breast cancer patients met during their hospital staying reveals that hope is an essential aspect of the ability to cope with the illness. Furthermore, our analysis confirms that hope can be placed on a continuum between Cognitive and Emotional dimensions, from the intersections of which 4 possible scenarios (Despairing Space, Fleeting Space, Hesitating Space and Hoping Space) can be identified.

Development and Evaluation of the Cancer Dyads Group Intervention: Preliminary Findings

Despite the fact that importance of primary relationships for cancer patients and their caregivers’ adaptation to illness is well recognized, only a paucity of studies report about clinical interventions for the patient–caregiver dyad. The article presents the Cancer Dyads Group Intervention (CDGI), a supportive group intervention for breast cancer patients and caregivers, and preliminary findings about its effectiveness. A correspondence analysis of the verbatim transcripts of the first three groups was conducted. Findings highlight the evolution of participants during the intervention and confirm the congruence between goals and the participants’ experience. Further investigation of the CDGI effectiveness is necessary.

Promoting Patient and Caregiver Engagement to Care in Cancer

The positive outcomes associated with Patient Engagement (PE) have been strongly supported by the recent literature. However, this concept has been marginally addressed in the context of cancer. Limited attention has also received the role of informal caregivers in promoting physical and psychological well-being of patients, as well as the interdependence of dyads. The Cancer Dyads Group Intervention (CDGI) is a couple-based psychosocial intervention developed to promote engagement in management behaviors, positive health outcomes, and the quality of the relationship between cancer patients and their informal caregivers. The article examines the ability of the CDGI to promote adaptive coping behaviors and the perceived level of closeness by comparing cancer patients participating in the intervention and patients receiving psychosocial care at usual. Results indicate that individuals diagnosed with cancer attending the CDGI present significant increases in Fighting Spirit and Avoidance, while reporting also reduced levels of Fatalism and Anxious Preoccupation. Initial indications suggest that the intervention may contribute to strengthening the relationship with the primary support person.