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Recruiting NCT06795815

The Implementation of the Go Wish Game to Promote Advance Care Planning in Onco- Hematologic Disease

No phase Interventional Leukemia Multiple Mieloma Advanced Solid Tumors Lymphoma

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Go Wish Game.
Who it may be relevant to
Registry conditions: Leukemia, Multiple Mieloma, Advanced Solid Tumors, Lymphoma. Basic parameters: 18 years — 99 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Implementation of the Go Wish Game to Promote Advance Care Planning in Onco-hematologic Disease (Onco-hema Go Wish-ACP): Intervention Set up and Multicentre Feasibility Trial

Overview

This is a mixed-method, device-free and drug-free multicenter interventional study. The study aims at facilitating end-of-life conversations within the doctor-patient relationship through the use of the Go Wish Game (GWG) and supporting patients, their caregivers and healthcare professionals to complete Advance Care Panning documentation. The GWG helps people clarify and identify their priorities, should they be affected by a chronic, disabling and potentially non-healing illness. In fact, the GWG consists of a small deck of cards, and on each card is a concrete action or situation that may be important to a person at the end of life. The "Onco-hema Go wish-ACP" project aims to evaluate the feasibility of a Go Wish Game-based intervention with patients with refractory lymphoma, leukemia or multiple myeloma or advanced solid tumors with prognosis \> 3 months. In terms of secondary objectives, the study aims to. * Evaluate and compare the intervention with hematology and oncology patients in terms of: - Other feasibility indicators; Involvement in CCP pathways; Quality of communication; Meaning of life; Impact on hope; through a series of questionnaires administered to patients and caregivers involved in the intervention * Qualitatively assess the acceptability of the intervention in terms of recruitment and delivery with patients and caregivers through semi-structured interviews and with professionals through Focus Groups (FGs). * To analyze the clinical records of enrolled patients in terms of: values and preferences; awareness of prognosis; end-of-life choices and shared decision-making on treatment decisions.

Interventions

  • Other Go Wish Game
    The Go Wish Game (GWG) provides a simple tool, composed by 35 cards to identify individual priorities. GWG is welcomed as a first step in clarifying values and personal thoughts linked to the end of life. The GWG discussion will be divided into two meetings. During the first one, the physician instructs the patients and their caregivers on how the GWG works. The patient will be invited to divide the cards into three sets, labeling the content of the cards within each set as: Very important;more

Primary outcome measures

  • Intervention Feasibility [Time frame: 1 Year]
Secondary outcome measures (6)
  • ACP Engagement; [Time frame: 18 Months]
  • Quality of Communication; [Time frame: 18 Months]
  • Meaning of Life; [Time frame: 18 Months]
  • Impact on patients' hope [Time frame: 18 Months]
  • Acceptability [Time frame: 18 Months]
  • ACP documentation [Time frame: 18 Months]

Eligibility criteria

Inclusion criteria

  • ≥ 18 years age; diagnosed with refractory lymphomas, or leukemia or multiple myeloma or advanced solid tumors and estimated prognosis > 3 months;
  • able to communicate in Italian and
  • to give written consent to the study.

Exclusion criteria

  • Patients with severe cognitive impairment or serious psychiatric condition;
  • refusal to participate to the study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Health services research

Study locations

Italy · 1 center
  • AziendaUSL IRCCS Reggio Emilia — Reggio Emilia

Identifiers

NCT: NCT06795815 · OHGW-ACP

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗