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RecruitingNCT06795815OHGW-ACPUpdated May 7, 2026

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

An interventional study of Go Wish Game in Leukemia, Multiple Mieloma and Advanced Solid Tumors, sponsored by Azienda USL Reggio Emilia - IRCCS. Recruiting at 1 site in Italy. Open to participants aged 18 Years to 99 Years. Per ClinicalTrials.gov, last updated 2026-05-07.

Sponsored by Azienda USL Reggio Emilia - IRCCS · Not applicable, Interventional, and Health services research

From the registry’s dates

  • Primary completion was expected by Jul 2026, 4 months ago, but the record still lists the study as recruiting.
  • Started Jun 2025; still recruiting 1 year 4 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
75
Allocation
Not applicable
Ages
18 Years to 99 Years
Sex
All
01

Study summary

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.
02

Conditions studied

  • Leukemia
  • Multiple Mieloma
  • Advanced Solid Tumors
  • Lymphoma
  • Oncology
  • Hematologic Diseases

Keywords

  • Advance Care Planning
  • Go Wish Game
  • Medical Oncology
  • Hematology
  • Oncology
  • Palliative Care
  • Experimental Design Study
  • Mixed Methods
03

In context

Leukemia

2,381 studies on the registry are indexed under Leukemia; 253 are open to participants now.

This study's planned enrollment of 75 is above the median of 40 across 1,769 interventional studies indexed under Leukemia.

Browse Leukemia studies →

Lead sponsor

Azienda USL Reggio Emilia - IRCCS is the lead sponsor of 93 studies on the registry; 26 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 99 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • ≥ 18 years age; diagnosed with 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

Exclusion Criteria:

  • Patients with severe cognitive impairment or serious psychiatric condition;
  • refusal to participate to the study
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Relapsed and refractory

Relapsed: the illness came back after treatment had worked. Refractory: it did not respond to treatment, or stopped responding while still on it.

05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
75 participants (estimated)

Study arms

  • Experimental
    Patients affected by refractory lymphomas, or leukemia or myeloma multiple or advanced solid tumors

    Other: Go Wish Game

Interventions

  • OtherGo 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 or less important and not important. This will be the base for the second meeting. During the second meeting - scheduled within one week - each category of card sets will be discussed with patients and their caregivers. The identification of the most relevant wishes or priorities of each patient will be incorporated into the individual therapeutic plan and the patient will be offered the option to make a formal ACP in the following 4 weeks.

06

What researchers measure

Primary outcomes

  1. Intervention Feasibility

    We will evaluate the feasibility of the intervention. Feasibility will be investigated by: 1. proportion of patients who will accept to participate among those screened/eligible who received the proposal to participate; 2. proportion of enrolled patients who will withdraw from the study after the first GWG discussion among the enrolled patients; 3, percentage proportion of enrolled patients who will attend all the planned GWG discussions; 4\. proportion of enrolled patients that will complete the ACP document (after participating in all the planned GWG discussions)

    Time frame: 1 Year

Secondary outcomes

  1. ACP Engagement;

    We will further assess and compare the intervention within hemato-oncological and oncological patients in terms of: 1\. ACP engagement: we will use the 4-item ACP Engagement (4-item ACP-E) questionnaire

    Time frame: 18 Months

  2. Quality of Communication;

    We will further assess and compare the intervention within hemato-oncological and oncological patients in terms of: 2\. Quality of communication: we will use the 19-item Quality of Communication (QOC) questionnaire

    Time frame: 18 Months

  3. Meaning of Life;

    We will further assess and compare the intervention within hemato-oncological and oncological patients in terms of: 3\. Meaning of life: we will use the Meaning in Life scale (MLS)

    Time frame: 18 Months

  4. Impact on patients' hope

    We will further assess and compare the intervention within hemato-oncological and oncological patients in terms of: 4\. Impact on patients' hope: we will use the Hope Herth Index (HHI)

    Time frame: 18 Months

  5. Acceptability

    5\. Acceptability of intervention in terms of recruitment and intervention delivery will be further investigated by: semi-structured interviews with patients and caregivers and FG with HPs who applied the GWG. .

    Time frame: 18 Months

  6. ACP documentation

    We will analyze the ACP documentation of patients enrolled to qualitatively investigate the congruence and relations between the priorities defined during the GWG meetings and the decisions written in the care plan

    Time frame: 18 Months

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Yes — We share individual information about gender, age, work occupation, disease type, prognosis and time of diagnosis.

Supporting information: Study protocol, Statistical analysis plan, Clinical study report, Analytic code

Access criteria: The access will be able only to those people in terms of clinical staff, who are involved in the study

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 7, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06795815
Lead sponsor
Azienda USL Reggio Emilia - IRCCS
Responsible party
Sponsor
First posted
Jan 28, 2025
Start date
Jun 30, 2025
Primary completion
Jul 2026 (estimated)
Completion
Jul 2026 (estimated)
Last update
May 7, 2026

Study contacts

Marta Perin (Dr), PhD
Contact
marta.perin@ausl.re.it
+39 3463576133
Andrea Fusco, MSc
Contact
andrea.fusco@ausl.re.it
+39 3409136595

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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