A scoping review of qualitative studies about children experiencing parental separation

Childhood ◽  
2012 ◽  
Vol 20 (2) ◽  
pp. 260-282 ◽  
Author(s):  
Rachel Birnbaum ◽  
Michael Saini
Author(s):  
Elīna Zelčāne ◽  
Anita Pipere

In the field of psychology resilience of the chronically ill has been studied mostly using quantitative research methods, but there are much fewer qualitative studies. This scoping review aims to collect definitions of resilience, find out, whether resilience development strategies are mentioned and what research approaches are used in qualitative studies about the resilience of the chronically ill. The review was conducted, following the 5-stage framework by Arksey and O’Malley, PRISMA guidelines, and searching in PubMed, PsychInfo, and Scopus databases. The main keywords (patients with chronic illness, resilience, strategies, qualitative studies) were selected according to the Participants/Concept/Context (PCC) framework, 21 articles were included in the review. Resilience mostly was defined as the ability to recover, return to normality, and adapt to new conditions after experiencing stress, illness, or other negative events. In several studies, other terms like coping, personal strength, self-management, and psychological growth were used instead. Lived experiences of the chronically ill show that resilience is not a stable ability, it changes over time. Resilience can be developed, using different strategies, such as having a positive mindset, learning new skills, accepting help, or promoting a healthy lifestyle. Qualitative content analysis and thematic analysis were the most often used research approaches in qualitative studies about the resilience of the chronically ill.  


Author(s):  
Ana Fernandez-Araque ◽  
Julia Gomez-Castro ◽  
Andrea Giaquinta-Aranda ◽  
Zoraida Verde ◽  
Clara Torres-Ortega

The aim of this review was to demonstrate the presence of categories and subcategories of Mishel’s model in the experiences of patients with fibromyalgia by reviewing qualitative studies. Uncertainty is defined as the inability to determine the meaning of disease-related events. A scoping review of qualitative studies was carried out. Twenty articles were included, with sample sizes ranging from 3 to 58 patients. Articles from different countries and continents were included. Three categories of the model and eight subcategories could be shown to be present in the experiences of fibromyalgia patients through the scoping review. The first category, concerning antecedents of uncertainty in patients with fibromyalgia, is constituted by the difficulty in coping with symptoms, uncertainty about the diagnosis and uncertainty about the complexity of the treatment. The second concerns the cognitive process of anxiety, stress, emotional disorder and social stigma. The third category refers to coping with the disease, through the management of social and family support and the relationship with health care professionals.


2020 ◽  
Vol 11 ◽  
Author(s):  
Karen Kengne Kamga ◽  
Jantina De Vries ◽  
Seraphin Nguefack ◽  
Syntia Nchangwi Munung ◽  
Ambroise Wonkam

2020 ◽  
Vol 78 (1) ◽  
Author(s):  
Saber Azami-Aghdash

Abstract Background A considerable number of qualitative studies have been published in recent years on the issues that the quantitative studies have limitations on. This study aimed at performing a meta-synthesis on qualitative studies on Road Traffic Injuries (RTIs) with a scoping review approach. Methods This meta-synthesis study was conducted as a scoping review in 2019. The Arkesy and O’Malley framework was applied which has six steps of identifying the research question, identifying the relevant studies, selecting the studies, charting the data, data analysis and reporting the results, and consultation exercise. The required data were gathered by searching the relevant keywords in databases of PubMed, web of knowledge, Scopus, Cochrane Library, Science Direct, Google scholar, Sid, IranMedex. Extracted data were analyzed by the Content-Analysis method. Results Finally, 30 studies were included. Extracted data summarized in five main themes and 17 sub-themes. The main themes were: consequences (individual, family, social, financial), the needs of survivors (social support and healthcare), risk factors (general risk factors, risk factors for motorcyclists, risk factors for children and adolescents), barriers of prevention (general barriers, pre-hospital barriers, emergency, and hospital barriers), and prevention solutions (increasing safety, rules and regulations, education, increasing equipment, scientific solutions) of RTIs. Conclusion This study combined the methods of the scoping review and the meta-synthesis to mapping all qualitative studies on the RTIs, with this approach, this study provides extensive and practical information for policy-makers, managers, practitioners, and researchers in the field of RTIs. Also, by applying this approach, the gaps in the existing knowledge and areas in need of further research are identified.


2020 ◽  
Author(s):  
Olmo Van den Akker ◽  
Gjalt - Jorn Ygram Peters ◽  
Caitlin Bakker ◽  
Rickard Carlsson ◽  
Nicholas Alvaro Coles ◽  
...  

This Systematic Review Registration Form is intended as a general-purpose registration form. The form is designed to be applicable to reviews across disciplines (i.e., psychology, economics, law, physics, or any other field) and across review types (i.e., scoping review, review of qualitative studies, meta-analysis, or any other type of review). That means that the reviewed records may include research reports as well as archive documents, case law, books, poems, etc. This form, therefore, is a fall-back for more specialized forms and can be used if no specialized form or registration platform is available.


2021 ◽  
Author(s):  
Susanne Jöbges ◽  
Corine Mouton-Dorey ◽  
Bara Ricou ◽  
Nikola Biller-Andorno

Abstract Background The use of coercion, which can be understood in a clinical context as imposing a measure against a patient’s opposition or declared will, can occur in various forms in intensive care units (ICU). One prime example of a coercive measure in the ICU is the use of restraints, which are applied for patients` own safety and for the protection of caregivers. A scoping review was conducted to explore the empirical data available on the experiences of ICU patients with coercive measures.Main text For this scoping review, clinical databases (PubMED, EMBASE, PsychINFO, Web of Science Core Collection, CINAHL, Scopus and Cochrane Library) were searched for qualitative studies. Using the CASP criteria for qualitative studies, the review focused on empirical research that captured how ICU patients themselves experienced restraints or other forms of coercion and excluded research related to staff experiences. A total of nine studies could be retrieved that fulfilled the inclusion criteria.The review describes common themes emerging from the scarce studies on patient experiences, including communication issues, delirium, memory, and emotional reactions. In spite of their serious clinical condition and fluctuating states of consciousness, a part of the patients did have memories of their ICU stay. Statements from patients revealed feelings of compromised autonomy and dignity that came with a loss of control. Physical restraints were only one concrete manifestation of coercion as perceived by patients in the ICU setting. Conclusion To date, there are few qualitative studies focusing on patient experiences of coercive measures in the ICU. In addition to the experience of restricted physical movement, the perception of loss of control, loss of dignity and loss of autonomy suggests that restraining measures are just one element in a setting that may be perceived as coercive. Health professionals may underestimate how deeply patients are affected by the perception of coercion. Good communication that clearly explains unavoidable measures to patients can reduce the negative impacts of coercive measures. More research on patient experiences is needed in order to reach a more comprehensive understanding of how patients perceive their ICU stay and to identify opportunities for further improvement of intensive care.


Pharmaceutics ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1100
Author(s):  
Kirsi Kvarnström ◽  
Aleksi Westerholm ◽  
Marja Airaksinen ◽  
Helena Liira

Introduction: Medication adherence continues to be a significant challenge in healthcare, and there is a shortage of effective interventions in this area. This scoping review studied the patient-related factors of medication adherence. Methods: We searched Medline Ovid, Scopus, and Cochrane Library from January 2009 to June 2021 to find the most recent original qualitative studies or systematic reviews that addressed the patient-related factors of medication adherence in treating chronic conditions. We used the PRISMA-ScR checklist to ensure the quality of the study. Results: The initial search revealed 4404 studies, of which we included 89 qualitative studies in the scoping review. We inductively organized the patient-related factors causing barriers, as well as the facilitators to medication adherence. The studies more often dealt with barriers than facilitators. We classified the factors as patient-specific, illness-specific, medication-related, healthcare and system-related, sociocultural, as well as logistical and financial factors. Information and knowledge of diseases and their treatment, communication, trust in patient-provider relationships, support, and adequate resources appeared to be the critical facilitators in medication adherence from the patient perspective. Discussion and conclusions: Patients are willing to discuss their concerns about medications. Better communication and better information on medicines appear to be among the critical factors for patients. The findings of this scoping review may help those who plan further interventions to improve medication adherence.


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