Skip to content

Impact of a Booklet-Question List on Cancer Patients or Their Families Seeking Prognostic Information During a Palliative Care Consultation

Impact of a Booklet-Question List on Cancer Patients or Their Families Seeking Prognostic Information During a Palliative Care Consultation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02854293
Acronym
QUEPAL
Enrollment
121
Registered
2016-08-03
Start date
2012-05-31
Completion date
2015-05-31
Last updated
2025-11-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metastatic Cancer, Palliative Care

Keywords

palliative care, cancer, quality of life

Brief summary

Prospective, randomized, multicentre phase III study to evaluate the level and type of information requested by patients or families during a palliative care consultation after they have been given the Booklet-Question List (BQL).

Interventions

OTHERBooklet-Question List

Booklet-Question List (BQL) proposed in palliative cares, divided into 8 chapters, given to the patient before the first palliative care consultation. Providing a list of questions to patients and their families without any obligations allows individual adaptation of information; patients or families who are afraid of asking these questions can take advantage of this opportunity, while respecting the need to avoid these subjects for other patients

Sponsors

Institut Curie
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient over the age of 18 years, * Patient who has signed the informed consent form after being given a written information sheet * Patient followed for metastatic cancer with or without specific treatment, with a limited life expectancy * Patient referred to the palliative care team. * French-speaking Patient

Exclusion criteria

* Cognitive disorders * Documented psychiatric disorders or marked psychological fragility

Design outcomes

Primary

MeasureTime frame
The number of questions asked or the concerns expressed that elicit a medical comment by the patient or the family during the palliative care consultation.one month

Secondary

MeasureTime frameDescription
HADS (Hospital Anxiety and Depression Scale) anxiety and depression scoreone month
QLQC-15Pal palliative quality of life scoreone monthThe EORTC QLQ-C15-PAL is a questionnaire developed to assess the quality of life of palliative cancer care patients
MB coping questionnaire scoreone monthThe Brief COPE is the abbreviated version of the COPE Inventory and assesses dispositional as well as situational coping efforts . The 28-item Brief COPE (consisting of 14 subscales) has acceptable psychometric properties and has been used extensively to examine the relationship between various coping strategies and psychological outcomes
Two 5-point Likert scales on information needs and satisfaction with medical informationone month
Specific questionnaire on the Booklet-Question List (mode of use, satisfaction)one month

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026