Training Model to Advance Support of the Family as a Caregiving System in the Inpatient Oncology Setting
Working with the Caregiving Family (WCF) training
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Supportive Care Study
Summary
Study start date: February 1, 2013
Actual date on which the first participant was enrolled.The purpose of this study is to provide a communication training program to inpatient nurses and social workers at Memorial Sloan Kettering Cancer Center in order to help them assist caregiving families. The importance of this training program is that it aims to teach nurses and social workers how and when to respond more effectively and compassionately to challenges faced by caregiving families. One of the goals of this program is to address family support needs during a patient's hospitalization.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.80 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 12 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Inclusion Criteria: Participating Providers: Provider is an MSKCC acute care advanced practice nurse and/or inpatient social worker as per self-report. Plans to attend at least 4/6 the didactic training sessions, and 3/6 consolidation sessions as per self-report. A patient will be approached if: Patient has been admitted to an inpatient service at MSKCC. Patient is able to designate at least one close person who is involved in the patient's care and is willing to participate. In the case that the patient is a minor (age 7-17 yrs), s/he will need to designate at least one close, adult person who is involved in the patient's care and is willing to participate. Family members will be approached if: They were identified as a close other (including a family friend) involved in the care of an admitted patient on a participating provider's floor Exclusion Criteria: Evidence of cognitive impairment severe enough to preclude completing survey instruments as per clinical or research staff judgment or EMR. Determined to not be appropriate for this study as per clinical judgment. Anyone, patient or family member, who is younger than 12 years old. Anyone, patient or family member, who does not speak English.
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Memorial Sloan Kettering Cancer Center
New York, United StatesOpen Memorial Sloan Kettering Cancer Center in Google Maps