[Solved]What are the experiences, preferences for and access to support for BME patients diagnosed with cancer and their caregiver

  100% Pass and No Plagiarism Guaranteed

[Solved]What are the experiences, preferences for and access to support for BME patients diagnosed with cancer and their caregivers from the time of diagnosis in the UK?

This scoping review should be succinct and will use the Arskey and O`Malley (2005) format. It should be 3000 words. Use tables, see uploaded document format and presentation please.
See the uploaded document, which is the style and content presentation of the document I would expect you to deliver. 
The aim of this scoping review is to identify gap in knowledge and the research needs for the cancer survivorship experiences of the Black African and Caribbean (BAC) individuals and their lay caregivers in the United Kingdom (UK) from the time of diagnosis for breast, colorectal, lung or prostate cancer.
The review question should be guided by the `SPICE` principle.
Suggested review question could be: `What are the experiences, preferences for and access to support for BME patients diagnosed with cancer and their caregivers from the time of diagnosis in the UK?
I will expect you to include global studies published in English between 2007 and October 2017 as papers published earlier than 2007 may not capture or reflect the UK National Cancer Survivorship Initiatives announced in Cancer Reform Strategy (2007) (Macmillan Cancer Support, 2008, and Foster and Fenlon, 2011). 
Suggested Search Terms Key words
Cancer type 

Population Breast cancer, lung cancer, colorectal/bowel cancer, prostate cancer, neoplasm and gynaecological cancer.
Caregiver, family, cancer survivor, partner, lay caregiver, friend, colleague, 
Stage of disease Survivorship, post treatment, living with and beyond cancer, and after treatment.
Ethnicity Ethnicity, hard-to-reach, BME, African, Caribbean, Afro-Caribbean, black, white, and black women.
Support

Setting
Type of study Self-management, information needs, psychosocial needs , follow-up, social support, support service, self-help seeking and culturally tailed services.
Hospital, cancer clinic, cancer support group, church, community.
Qualitative, quantitative, survey, cross-sectional, longitudinal,
Other search terms Culture and healthcare, culture and cancer, culture and adaptation, BME cancer survivors’ and care access, and disparity in access. 

When writing the review background, themes should include Cancer statistics and pathway in the UK, BME and cancer survivorship in the UK, Cancer health policies in the UK, the debate on the definition of cancer survivorship, social support following cancer diagnosis and focus on Black African and Caribbean population in the UK.

The search should be from the time of diagnosis.
The focus is on only the four common cancers, lung, breast, colorectal and prostate cancers.

The themes for the review results could reflect the experiences of BME cancer survivors in the UK, their preferences for support, how they access support, barriers and facilitators of their access to support and the lived experiences of their lay caregivers, etc.

Conduct comprehensive systematic searches across electronic databases related to health, social care and nursing such as EMBASE, MEDLINE, CINAHL, PhyscoINFO, Web of Science, ProQuest, Scopus, Google Scholar and cancer websites.