Identifying Family Members in Need of Support While Caregiving and After Loss

Memorial Sloan Kettering Cancer Center (MSK)

Status: Active, not recruiting

Conditions: Advanced Cancer

Treatments: Behavioral: bereavement risk screening tool; Behavioral: background questionnaire

Study type: Observational

Funder types: Other

Identifiers

NCT02455505

15-095

Details and patient eligibility

About

This screening tool will be used to identify significant relations of patients with advanced medical illness or serious hospitalization and family individuals who lost their loved one and who could use professional support in the future. We are interested in enrolling family members or close friends of patients with advanced medical illness as well as family members or close friends who have lost a loved one. Some screening tools to identify family members who might need support do exist, but the investigators are hoping to develop one that is brief and easier for healthcare providers to use. The information learned in this study will help us refine the screening tool. Family member input will be essential in the development of this screening tool.

Enrollment: 52 patients

Sex: All

Ages: 21+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• As per self-report, 21 years or older
• As per self-report, has a domestic partner or spouse, child (minor or adult), sibling (sister or brother), parent or close friend diagnosed with any advanced medical illness or who was recently (2 months) or is currently hospitalized for life-threatening injuries or conditions related to a traumatic incident (e.g., car accident, overdose, assault) OR
• As per self-report, experienced the recent (within 2 months to 3 years) death of a domestic partner or spouse, child (minor or adult), sibling, parent or close friend.
• Responds "yes" to the question "Can you understand spoken and written English?
• Agrees to be audio-taped during the cognitive interview [Waves 1 and 2 only] * For Part 2 only: In the event that the patient dies prior to a consenting pre-loss family member completing the study questionnaires, the family member will be eligible for participation in the post-loss group after at least 2 months have passed after the loss

Exclusion criteria

• Significant psychiatric or cognitive disturbance sufficient, in the investigators' judgment, to preclude the completion of the assessment measures or informed consent (i.e., acute psychiatric or neurological symptoms which require individual treatment)
• Another family member (parent, domestic partner or spouse, sibling, or adult child) has been enrolled in the study

Trial design

52 participants in 1 patient group

Risk Screening tool & Cognitive Interview

Treatment:

Behavioral: background questionnaire

Behavioral: bereavement risk screening tool