DEQOLAGE: Determinants of Quality Of Life in AGEd Cancer Patients

Sponsor
Assistance Publique - Hôpitaux de Paris (Other)
Overall Status
Unknown status
CT.gov ID
NCT02672657
Collaborator
Research Team CEpiA (Clinical Epidemiology and Ageing) EA7376, University Paris Est Créteil (UPEC) (Other), Research Team APEMAC EA4360, University of Lorraine (Other), Unité de Recherche Clinique Mondor, Hôpital Henri Mondor (Other), Institut de Cancérologie de Lorraine (Other), Unité de Coordination en Onco-Gériatrie (UCOG) Sud Val-de-Marne (Other), Quality of life and cancer clinical research platform (Other), Ligue contre le cancer, France (Other), Conseil Régional de Lorraine, France (Other)
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Study Details

Study Description

Brief Summary

Patients face multiple stresses and challenges in the aftermath of cancer diagnosis. Despite needs perceived by elderly patients might differ from those of younger patients, there is a paucity of published data assessing the specific evolution and relevant determinants of health-related quality of life (HRQoL) in older patients with cancer. Such determinants may include cancer type/location/stage, treatment type/intensity, comorbidities, nutritional status or socioeconomic features, but also practical organization of care -frequency, geographical distance, supporting measures -, or psychosocial and material support - social network, housing conditions and contextual neighborhood features. Comparatively to dementia or cancer in younger patients, little is known in the oncogeriatric field of the impact on caregivers' perceived burden and HRQol of the support they provide to patients. Further, the potential interactions between patients' and caregivers' HRQoL remain largely unknown, while caregivers are often themselves old with chronic diseases and/or daily living activities' limitations.

The DEQOLAGE study is a prospective observational cohort study that aims to describe the HRQoL of patients aged over 70 years with a colorectal or prostatic cancer during the first year following the diagnosis of the disease as well as the HRQoL and burden in their main caregivers. This study will allow a comprehensive assessment of multiple determinants of HRQoL operating at different levels, including individual (cancer type/location/stage, treatment type/intensity, comorbidities, nutritional status or socioeconomic features), contextual (social network, housing conditions and contextual neighborhood features) and organizational factors (frequency, geographical distance, supporting measures). We also hypothesize that complex interactions may operate between patient's and caregiver's HRQoL and perceived burden. Quality of life measurement will be based on two recent scales specifically designed for the elderly to confirm their psychometric properties and in-field feasibility.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    300 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Assessing the Evolution and Determinants of Quality of Life in Elderly Cancer Patients and Their Caregivers: a Prospective Multicenter Observational Cohort Study.
    Study Start Date :
    Feb 1, 2016
    Anticipated Primary Completion Date :
    Feb 1, 2019
    Anticipated Study Completion Date :
    Dec 1, 2019

    Outcome Measures

    Primary Outcome Measures

    1. Changes in HRQoL of patients and their caregivers as assessed by the generic WHOQOL-BREF questionnaires [At baseline, 3, 6, and 12 months]

    2. Changes in HRQoL of patients and their caregivers if aged >70 years as assessed by the WHOQOL-OLD questionnaire [At baseline, 3, 6, and 12 months]

    3. Changes in HRQoL of patients as assessed by the specific EORTC-QLQ C30 questionnaire [At baseline, 3, 6, and 12 months]

    4. Changes in HRQoL of patients as assessed by the specific EORTC QLQ-ELD14 questionnaire [At baseline, 3, 6, and 12 months]

    5. Changes in burden of patients' caregivers as assessed by the Zarit burden inventory questionnaire [At baseline, 3, 6, and 12 months]

    Secondary Outcome Measures

    1. Psychometric properties of the HRQoL questionnaire WHOQOL-OLD (validity, reliability, sensitivity to change, feasibility) [At baseline, 3, 6, and 12 months]

    2. Psychometric properties of the HRQoL questionnaire EORTC QLQ-ELD14 (validity, reliability, sensitivity to change, feasibility) [At baseline, 3, 6, and 12 months]

    3. Prognostic value of baseline HRQoL measurements on cancer progression-free survival [At baseline, 3, 6, and 12 months]

    4. Prognostic value of baseline HRQoL measurements on overall survival [At baseline, 3, 6, and 12 months]

    5. Prognostic value of baseline HRQoL measurements on patient's functional decline, defined as any decrease in the ADL scale [At baseline, 3, 6, and 12 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    70 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    Patients

    Inclusion Criteria:
    • Aged 70 or more

    • With a new histologically confirmed diagnosis of colorectal or prostate cancer

    • With a Comprehensive Geriatric Assessment (CGA) performed before the initiation of cancer treatment

    • Having expressed their oral non-opposition to participate in the study

    • Affiliated to a health insurance scheme

    Exclusion Criteria:
    • Expected survival inferior to 6 months, based on the clinical appreciation from the physician in charge of the enrollment

    • Cancer recurrence in patients previously treated

    • Physical, cognitive or linguistic incapacity to complete questionnaires

    Caregivers Inclusion criteria

    • Aged 18 or more

    • Nonprofessionally, partially or fully helping the patient in daily activities and accompanying the patient to visits; familial ties with the patient are not required (spouse, child, friend or neighbor)

    • In contact with the patient more than once a week

    • Defined by the patient during the inclusion visit as the main caregiver

    Exclusion criteria

    • Physical, cognitive or linguistic incapacity to complete questionnaires

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hôpital Henri Mondor Créteil France 94010
    2 CHRU Nancy Nancy France 54000
    3 Hôpital Saint Louis Paris France 75010

    Sponsors and Collaborators

    • Assistance Publique - Hôpitaux de Paris
    • Research Team CEpiA (Clinical Epidemiology and Ageing) EA7376, University Paris Est Créteil (UPEC)
    • Research Team APEMAC EA4360, University of Lorraine
    • Unité de Recherche Clinique Mondor, Hôpital Henri Mondor
    • Institut de Cancérologie de Lorraine
    • Unité de Coordination en Onco-Gériatrie (UCOG) Sud Val-de-Marne
    • Quality of life and cancer clinical research platform
    • Ligue contre le cancer, France
    • Conseil Régional de Lorraine, France

    Investigators

    • Study Chair: Christine Perret-Guillaume, CHU de Nancy
    • Study Chair: Elena Paillaud, Hôpital Albert Chenevier

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Assistance Publique - Hôpitaux de Paris
    ClinicalTrials.gov Identifier:
    NCT02672657
    Other Study ID Numbers:
    • 2014-A00317-40
    First Posted:
    Feb 3, 2016
    Last Update Posted:
    Aug 26, 2016
    Last Verified:
    Aug 1, 2016
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by Assistance Publique - Hôpitaux de Paris
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 26, 2016