Trial of Family Focused Grief Therapy in Palliative Care and Bereavement
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Details and patient eligibility
About
The purpose of this study is to learn how well family therapy works if given while a family member is being treated for a serious illness and whether it helps their family to continue meeting for a time after their death. The therapy aims to assist the family communication and support during both palliative care and bereavement. The investigators also want to learn how many family therapy sessions spread out over time are best for helping patients and their families.
Patients are randomly assigned to one of three groups: patients who receive standard palliative care, patients and their families who take part in 6 sessions, and patients and their families who take part in 10 sessions.
Full description
This Randomized Controlled Trial (RCT) seeks to test the efficacy and dose responsiveness of a manualized family therapy intervention called Family Focused Grief Therapy (FFGT), which is delivered to families of patients with advanced disease and continued into bereavement. Randomization is to three arms: 6 sessions of FFGT, 10 sessions of FFGT, or standard care. The study also explores the potential mediators of effective outcome, empowering further refinement of the intervention, and undertakes an analysis of health-related costs of bereavement care. It is a multi-site study involving Memorial Hospital for Cancer and Allied Diseases (a comprehensive cancer center), Calvary Hospital (a dedicated palliative care hospital with home hospice care program)and Beth Israel (a medical center with a dedicated pain and palliative care department. Consenting families will be assessed at baseline through completion of questionnaires that appraise each individual's psychosocial well-being and perception of their family's functioning. Therapy will be delivered by family therapists (social workers, psychologists, and psychiatrists), who will attend regular supervision sessions to sustain fidelity of the model of intervention. Follow-up of family members for psychosocial well-being, perceptions of family functioning, and costs of heath-related care will occur at 3, 6, 9, & 13 months after the patient's death or completion of therapy sessions.
Enrollment
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Volunteers
Inclusion criteria
Subject/Patient Inclusion Criteria
- Individuals with advanced disease/Stage 4-IV cancer who may be involved in palliative care treatment program.
- Individuals with a poor prognosis Patient and Family Member Inclusion Criteria.
- Per investigator's judgment participants must have satisfactory cognitive functioning to provide valid informed consent and participate in family therapy.
- In the event that the index family member is declining or too frail to take part in family meetings, the family is able to participate without the index patient being involved in the study.
- For every enrolled family there must be at least 2 family members willing/able to take part at the time of recruitment.
- The presence of FRI screening scores of ≤ 9 or cohesiveness subscale score < 4 based on the perception of any single family member, including the patient.
Exclusion criteria
- Inability through language to complete the study questionnaires - inability to speak English with an English-speaking therapist.
- Age less than 12 years old for a child.
- Patient and family member determined geographical inaccessibility to attend family sessions.
- Significant psychiatric disturbance sufficient, in the investigator's judgment, to preclude participation in a psychotherapeutic intervention.
Trial design
Primary purpose
Allocation
Interventional model
Masking
700 participants in 3 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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