The information needs of partners and family members of cancer patients: a systematic literature review.
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The Experience of Caregivers Living with Cancer Patients: A Systematic Review and Meta-SynthesisStudies analysing the need for health-related information in Germany - a systematic reviewUser-generated online health content: a survey of Internet users in the United Kingdom.Access family functioning and related factors from the viewpoints of male cancer patients.Adult Acute Myeloid Leukemia Long-term Survivors.Development of prognosis in palliative care study (PiPS) predictor models to improve prognostication in advanced cancer: prospective cohort study.Iranian caregivers, silent mediums in caring for relatives suffering from cancerA Systematic Review of Predictions of Survival in Palliative Care: How Accurate Are Clinicians and Who Are the Experts?A Family-Centered Model for Sharing Genetic Risk.Study Protocol: Evaluation of a DVD intervention designed to meet the informaton needs of patients with head and neck cancer and their partner, carer and families.Optimizing Social Network Support to Families Living With Parental Cancer: Research Protocol for the Cancer-PEPSONE Study.Cancer caregivers information needs and resource preferences.An Exploratory Study on the Information Needs of Prostate Cancer Patients and Their PartnersCare for the cancer caregiver: a systematic reviewAn Online Learning Module to Increase Self-Efficacy and Involvement in Care for Patients With Advanced Lung Cancer: Research Protocol.Racial and ethnic variation in partner perspectives about the breast cancer treatment decision-making experience.Do men with prostate cancer and their partners receive the information they need for optimal illness self-management in the immediate post-diagnostic phase?Improving couples' quality of life through a Web-based prostate cancer education intervention.Needs and Preferences of Partners of Cancer Patients Regarding a Web-Based Psychological Intervention: A Qualitative Study.Education given to parents of children newly diagnosed with acute lymphoblastic leukemia: a narrative review.A qualitative study exploring the experience of the partners of cancer survivors and their views on the role of primary care.The needs of informal caregivers of elderly people living at home: an integrative review.Prevalence, intensity, and predictors of the supportive care needs of women diagnosed with breast cancer: a systematic review.Patient-centred care: making cancer treatment centres accountable.Information and decision-making needs among people with mental disorders: a systematic review of the literature.An evidence-based stress management intervention for allogeneic hematopoietic stem cell transplant caregivers: development, feasibility and acceptability.Needs of caregivers of cancer patients: validation of the Mexican version of the Support Person Unmet Needs Survey (SPUNS-SFM).Facing spousal cancer during child-rearing years: The short-term effects of the Cancer-PEPSONE programme-a single-center randomized controlled trial.Measuring the quality of patient-centered care: why patient-reported measures are critical to reliable assessmentTransition to the new role of caregiving for families of patients with breast cancer: a qualitative descriptive exploratory study.Informal carers' experiences and needs when supporting patients through chemotherapy: a mixed method study.The method of nursing support in hospital and patients' and family members' experiences of the effectiveness of the support.No man's land: information needs and resources of men with metastatic castrate resistant prostate cancer.Shared decision-making and providing information among newly diagnosed patients with hematological malignancies and their informal caregivers: Not "one-size-fits-all".Fear of cancer recurrence and unmet needs among breast cancer survivors in the first five years. A cross-sectional study.Effects of a surgical ward care protocol following open colon surgery as part of an enhanced recovery after surgery programme.Levels of unmet needs and distress amongst adolescents and young adults (AYAs) impacted by familial cancer.The influence of family ties on men's prostate cancer screening, biopsy, and treatment decisions.A qualitative study of breast cancer treatment decisions: evidence for five decision-making styles.Preferences for cancer support group topics and group satisfaction among patients and caregivers.
P2860
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P2860
The information needs of partners and family members of cancer patients: a systematic literature review.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 29 April 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
The information needs of partn ...... systematic literature review.
@en
The information needs of partn ...... systematic literature review.
@nl
type
label
The information needs of partn ...... systematic literature review.
@en
The information needs of partn ...... systematic literature review.
@nl
prefLabel
The information needs of partn ...... systematic literature review.
@en
The information needs of partn ...... systematic literature review.
@nl
P2093
P1476
The information needs of partn ...... systematic literature review.
@en
P2093
Eike Adams
Eila Watson
Mary Boulton
P304
P356
10.1016/J.PEC.2009.03.027
P577
2009-04-29T00:00:00Z