2020
DOI: 10.1007/s00520-020-05743-z
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Empowering caregivers in the radiotherapy process: the results of a randomized controlled trial

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Cited by 11 publications
(44 citation statements)
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“…Length of individual contacts lasted between 15 min 57 to 2 h 50 . Many of the interventions were delivered via face‐to‐face contact in a hospital, often supplemented with telephone follow‐ups, 35,39,42,44,49,51,54,56,59 websites 38,48 and home visits 53 . Thirteen of the interventions were nurse‐led interventions 34–36,39,40,43,47,50,52–54,59 .…”
Section: Resultsmentioning
confidence: 99%
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“…Length of individual contacts lasted between 15 min 57 to 2 h 50 . Many of the interventions were delivered via face‐to‐face contact in a hospital, often supplemented with telephone follow‐ups, 35,39,42,44,49,51,54,56,59 websites 38,48 and home visits 53 . Thirteen of the interventions were nurse‐led interventions 34–36,39,40,43,47,50,52–54,59 .…”
Section: Resultsmentioning
confidence: 99%
“…Various caregiver‐reported outcomes were measured across studies such as QoL, depression, anxiety, caregiver burden, caregiving preparedness, supportive care needs and perceived stress. Fourteen studies reported a high Cronbach's alpha as an indicator for internal consistency for various measures for caregiver outcomes 15,35,38,41,42,44,46,48,54,56,57,59,61 . For instance, a Cronbach's alpha of 0.84 and 0.88 was reported for caregiver QoL cancer scale (CQOLC) 38 and Center for Epidemiological Studies‐Depression (CES‐D) 44 respectively.…”
Section: Resultsmentioning
confidence: 99%
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“…Such care is based on monitoring the patient's daily activities, taking psychosocial measures, taking medications, monitoring side effects, managing symptoms such as pain and shortness of breath, among others 23-24. However, a North American study 23 and a Colombian study 25 indicate that much is discussed about the benefits of psychosocial intervention on the caregiver, addressing, for example, coping, communication and problem solving strategies. But just a little is said about the absence in the literature of strategies that help caregivers in these aspects, or about the lack of training of the health team to act in the face of illness processes that mobilize an entire family nucleus [26][27] , main aspects taken into account in the elaboration of this research.…”
Section: Discussionmentioning
confidence: 99%
“…Today, cancer care has shifted more to outpatient and home care, and family caregivers (FCs) have become the leading provider of support for patients with cancer (2). Family caregivers often take various actions such as caring for the patient, managing symptoms, assisting with daily activities, and providing emotional support at home (3). They are often entrusted with the role of patient care without proper preparation and support, to the point where they do not even seek help for their own needs (4); leading them to undergo a significant burden of caring for the patient (5).…”
Section: Introductionmentioning
confidence: 99%