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Prognostic Understanding in ESC (ProgESC Study)

Prognostic Understanding in Patients Receiving Enhanced Supportive Care (ProgESC Study)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06067087
Enrollment
91
Registered
2023-10-04
Start date
2023-11-15
Completion date
2024-08-31
Last updated
2025-01-03

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

Conditions

Advanced Cancer

Keywords

Prognostic understanding, Enhanced Supportive Care Team, Quality of life, Anxiety, Depression, Satisfaction

Brief summary

This study aims to assess how aware patients with advanced cancer are about their prognosis when they are referred to an Enhanced Supportive Care (ESC) service. Further, the study aim to assess the relationship between patients prognostic understanding and their mental health, quality of life, trust in medical professionals as well as their perception of the care they receive. The study will involve adult patients with advanced cancer who are referred to the ESC service at London University College Hospital. Patients who agree to participate will provide consent and answer a questionnaire. The questionnaire will cover their prognostic awareness, psychological symptoms, and quality of life. It takes about 20 minutes to complete and can be done online via RedCap

Detailed description

Background: Prognostic awareness among patients with life-limiting diseases has been shown to be associated with less depression, better quality of care and earlier referral to palliative care. Moreover, accurate understanding of their illness may support patients to make informed decisions about their future in alignment with their preferences, values or needs. Supportive care in cancer is the prevention and management of the adverse effects of cancer and its treatment. This includes management of physical and psychological symptoms and side effects. Enhanced Supportive Care (ESC) is a relatively new initiative implementing early supportive care in patients with advanced cancer. Although studies have shown that a large proportion of patients with advanced cancer remain unaware that their disease is not curable, research regarding prognostic awareness in patients referred to Enhanced Supportive Care (ESC) services is still scarce. A deeper knowledge of the factors and patient characteristics associated with prognostic awareness is an important first step to develop interventions to improve prognostic communication and thereby to facilitate delivery of high-quality ESC. General aim: The ESC team at University College London Hospital is embedded within the oncology outpatient service, providing specialist symptom control and Advanced Care Planning to patients with advanced cancer. The primary aim of this study is to better understand the prognostic awareness of patients referred to the ESC service. A secondary aim is to evaluate the relationship between patients' prognostic awareness and levels of psychological distress, quality of life, trust in medical professionals and perceived quality of care. Patient population: Consecutive adult patients with advanced cancer referred to the ESC service will be eligible to participate. Patients unable to complete questionnaires due to cognitive impairment such as dementia will be excluded. Patients who have already been referred to community palliative care services will also be excluded. Methods: This will be a cross-sectional prospective study. Potentially eligible patients will be identified by members of the ESC team and will be informed about the study. Interested patients will then discuss the study with the research team and will be invited to participate. After informed consent has been obtained, participants will complete a questionnaire which will cover their level of prognostic awareness, psychological symptoms, and quality of life). The questionnaire will take approximately 20 minutes to complete. The questionnaire can be completed online via RedCap. Endpoints: The primary endpoint of this study is the level of patients' prognostic awareness, which will be assessed by the Prognosis and Treatment Perception Questionnaire. This questionnaire has previously been successfully used in research to assess patients' information preferences, perceptions about their prognosis and the goals of therapy and communication preferences about end-of-life care. Secondary endpoints will be (a) patients' preferences for receiving prognostic information assessed through the Prognosis and Treatment Perception Questionnaire (b) symptoms of depression evaluated through the Patient Health Questionnaire-2 (PHQ-2), (c) symptoms of anxiety evaluated through the Generalized Anxiety Disorder 2-item (GAD-2), (d) quality of life and (d) patients' trust in their medical team and (e) other aspects of perceived quality of care, rated on a visual analogue scale (NRS) from 0-10. Sample size and statistics: The investigators will conduct univariable and multivariable regression analyses to evaluate associations between sociodemographic or clinical variables and outcomes. The investigators aim to include 100 patients. This will give us at least 10 degrees of freedom to assess association of potential risk factors with outcome and to evaluate confounders in a multivariable analysis. Discussion: This will be the first prospective study to assess prognostic awareness among cancer patients referred to ESC services in a British setting. Identifying covariates for prognostic unawareness and psychological burden among patients with advanced cancer will inform the future development of strategies to improve care and communication with this patient group.

Interventions

None listed

Sponsors

University College, London
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

* All participants aged 18 and older with advanced cancer referred to the ESC team will be eligible for this study.

Exclusion criteria

* Younger than 18 years * Insufficient English language to complete questionnaires * cognitive impairment * Participants who, in the opinion of the member of the ESC team, would not be appropriate to participate

Design outcomes

Primary

MeasureTime frameDescription
Patients' prognostic understandingwithin 1 week after patient assessment by the Enhanced Supportive Care TeamPatients' prognostic understanding about their illness assessed through the Prognosis and Treatment Perception Questionnaire. This questionnaire assesses patient beliefs regarding the likelihood of cure, the preference for receiving prognostic information as well as the perceived helpfulness of knowing about prognosis

Secondary

MeasureTime frameDescription
Perceived value of prognostic informationwithin 1 week after patient assessment by the Enhanced Supportive Care TeamAssessed through the Prognosis and Treatment Perception Questionnaire. This questionnaire assesses patient beliefs regarding the likelihood of cure, the preference for receiving prognostic information as well as the perceived helpfulness of knowing about prognosis

Other

MeasureTime frameDescription
Patients' quality of lifewithin 1 week after patient assessment by the Enhanced Supportive Care TeamPatients' quality of life assessed through the European Organisation for Research and Treatment of Cancer quality of life core 15 palliative questionnaire. This 15-item questionnaire, employs a 4-point Likert scale for each question, and the resulting scores are linearly transformed to a possible range of 0 to 100, where higher scores indicate a better quality of life
Symptoms of anxietywithin 1 week after patient assessment by the Enhanced Supportive Care TeamPatients' symptoms of anxiety assessed through the Generalized Anxiety Disorder 2-item. This scale has a range from 0 to 6 points with higher scores indicating more symptoms of anxiety. A score of 3 points is considered a cut-off point, in which further evaluation is recommended.
Satisfaction with carewithin 1 week after patient assessment by the Enhanced Supportive Care TeamPatients' satisfaction with care assessed on a numeric rating scale ranging from 0-10 with higher scores indicating greater satisfaction
Trust in the treating oncologistwithin 1 week after patient assessment by the Enhanced Supportive Care TeamPatients' trust in the treating oncologist assessed on a numeric rating scale ranging from 0-10 with higher scores indicating more trust
Symptoms of depressionwithin 1 week after patient assessment by the Enhanced Supportive Care TeamPatients' symptoms of depression assessed through the Patient Health Questionnaire-2. This scale has a range from 0 to 6 points with higher scores indicating more depressive symptoms. A score of 3 points is considered a cut-off point, in which further evaluation is recommended.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026