Interventions with Family Caregivers of Cancer Patients: Meta-Analysis of Randomized Trials

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Items 201–300 of 854

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16. YouTube as a Tool for Pain Management With Informal Caregivers of Cancer Patients: A Systematic Review
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17. Physical and emotional well-being and support in newly diagnosed head and neck cancer patient–caregiver dyads
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18. Coping Skills Practice and Symptom Change: A Secondary Analysis of a Pilot Telephone Symptom Management Intervention for Lung Cancer Patients and Their Family Caregivers
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20. Family Caregivers’ Unmet Needs in Long-term Cancer Survivorship
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21. Effects of psychosocial interventions on psychological outcomes among caregivers of advanced cancer patients: a systematic review and meta-analysis
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22. Research Priorities in Geriatric Palliative Care: Informal Caregiving
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23. Psychosocial Impact of Cancer Patients on Their Family Members
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24. Stress, Coping, and Lived Experiences among Caregivers of Cancer Patients on Palliative Care: A Mixed Method Research.
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25. Unpacking the layers: a meta-ethnography of cancer survivors’ loneliness
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27. Deriving Meaning and Faith in Caregiving
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28. Trajectories of mental and physical functioning among spouse caregivers of cancer survivors over the first five years following the diagnosis
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29. Digital Health Psychosocial Intervention in Adult Patients With Cancer and Their Families: Systematic Review and Meta-Analysis
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30. Evaluation of a brief pilot psychoeducational support group intervention for family caregivers of cancer patients: a quasi-experimental mixed-methods study
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31. Empowerment from patient’s and caregiver’s perspective in cancer care
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32. Caregiver availability and patient access to hematopoietic cell transplantation: social worker perspectives inform practice
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33. The project ENABLE Cornerstone randomized pilot trial: Protocol for lay navigator-led early palliative care for African-American and rural advanced cancer family caregivers
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34. Sleep and Sleep-Wake Disturbances in Care Recipient-Caregiver Dyads in the Context of a Chronic Illness: A Critical Review of the Literature
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35. Understanding the Psychosocial Issues of African American Couples Surviving Prostate Cancer
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36. Acceptance and commitment therapy for patient fatigue interference and caregiver burden in advanced gastrointestinal cancer: Results of a pilot randomized trial
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37. The Effects of Exercise on Physical and Psychological Outcomes in Cancer Caregivers: Results from the RECHARGE Randomized Controlled Trial
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38. The experiences and needs of primary family caregivers of patients with multiple myeloma: A qualitative analysis
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39. Sharing in care: engaging care partners in the care and communication of breast cancer patients
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40. Contextual and Cultural Influences on Caregivers of Hispanic Cancer Survivors
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41. Patient-Centered Cancer Treatment Planning: Improving the Quality of Oncology Care: Workshop Summary
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42. The Science of Caregiver Health
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43. A qualitative study exploring the experience of the partners of cancer survivors and their views on the role of primary care
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44. Pilot Evaluation of the Impact of Structured Child-Centered Interventions on Psychiatric Symptom Profile of Parents with Serious Somatic Illness: Struggle for Life Trial
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45. Protocol for the Care-IS Trial: a randomised controlled trial of a supportive educational intervention for carers of patients with high-grade glioma (HGG)
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46. Needs and Preferences of Partners of Cancer Patients Regarding a Web-Based Psychological Intervention: A Qualitative Study
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47. Predictors of long-term distress in female partners of men diagnosed with prostate cancer
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48. Self-efficacy, social support, and quality of life among primary family-member caregivers of patients with cancer in Thailand
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49. Moving family interventions into the real world: What matters to oncology stakeholders?
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50. Investigating psychological problems in caregiver of pediatrics with cancer: A systematic review
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51. A randomized intervention involving family to improve communication in breast cancer care
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53. Development of a Symptom Management Intervention: Qualitative Feedback from Advanced Lung Cancer Patients and their Family Caregivers
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54. Implementing a Clinic-Based Telehealth Support Service (FamilyStrong) for Family Caregivers of Individuals with Grade IV Brain Tumors
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55. A mixed-methods qualitative research study to develop a complex intervention for weight loss and anorexia in advanced cancer: The Family Approach to Weight and Eating
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56. Effects of Caregiver-Focused Programs on Psychosocial Outcomes in Caregivers of Individuals with ASD: A Meta-analysis
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58. The role of symptom appraisal, concealment and social support in optimizing dyadic mental health in heart failure
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59. The effect of targeted palliative care interventions on depression, quality of life and caregiver burden in informal caregivers of advanced cancer patients: A systematic review and meta-analysis of randomized controlled trials
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70. Caregivers’ quality of life after blood and marrow transplantation: a qualitative study
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71. The Hidden Morbidity of Cancer
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72. Non-pharmacological Interventions for Caregivers with Depression and Caregivers of Care Recipients with Co-morbid Depression: Systematic Review and Meta-analysis
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75. Deploying the Behavioral and Environmental Sensing and Intervention for Cancer Smart Health System to Support Patients and Family Caregivers in Managing Pain: Feasibility and Acceptability Study
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84. Family caregivers of advanced cancer patients: self-perceived competency and meaning-making
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90. The impact of a problem-solving intervention on increasing caregiver assistance and improving caregiver health
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91. The Effects of a Patient-Caregiver Education and Follow-Up Program on the Breast Cancer Caregiver Strain Index
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