ITMO public health
Last update : 07/05/2015 | Version : 1 | ID : 8693
| General | |
| Identification | |
| Detailed name | Cross-sectional Study on Life Two Years After Cancer |
| Sign or acronym | VICAN 2 |
| CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation | CNIL: no. 911290 |
| General Aspects | |
| Medical area |
Cancer research |
| Health determinants |
Lifestyle and behavior Medicine Occupation Social and psychosocial factors |
| Keywords | upper aerodigestive tract, bladder, ALCL, cervix, body of uterus, healthcare consumption, clinical state, persistent physical and psychological effects, employment, LDD, cancer, breast, prostate, colorectal, healthcare system, social impact, social integration, lung, kidney, thyroid, melanoma, living conditions, quality of life |
| Scientific investigator(s) (Contact) | |
| Name of the director | Peretti-Watel |
| Surname | Patrick |
| Address | ORS PACA - UMR912 23 rue Stanislas Torrents 13006 Marseille |
| Phone | +33 (0) 4 91 59 89 00 |
| patrick.peretti-watel@inserm.fr | |
| Unit | UMR912 (SE4S) INSERM |
| Collaborations | |
| Funding | |
| Funding status |
Public |
| Details | INCa in partnership with CNAM-TS (National Health Insurance Fund for Salaried Workers), MSA (Social Security Scheme for Agricultural Workers) and RSI (Social Security Scheme for Independent Workers). |
| Governance of the database | |
| Sponsor(s) or organisation(s) responsible | INCa |
| Organisation status |
Public |
| Sponsor(s) or organisation(s) responsible | Inserm |
| Organisation status |
Public |
| Additional contact | |
| Main features | |
| Type of database | |
| Type of database |
Study databases |
| Study databases (details) |
Not-repeated cross-sectional studies (except case control studies) |
| Database recruitment is carried out by an intermediary |
A selection of health institutions and services |
| Database recruitment is carried out as part of an interventional study |
No |
| Additional information regarding sample selection. | Random national sample stratified by age (18-52 years/53-82 years) and location; selected from Long-Duration Disease files from three major health insurance schemes: CNAMTS, MSA and RSI. |
| Database objective | |
| Main objective |
The general objective is to investigate living conditions two years after cancer diagnosis, including:
— Perception of illness by affected individuals and their relationships with healthcare professionals (diagnosis verbalisation, recovery perception, disclosure of illness, access to information, participation in treatment choice); — Quality of life two years after onset of illness, psychological issues and professional support obtained; — lmpact on social life (professional activity, income, discrimination) and private life (couple relationships, sex life, parenting, help from those close to individual). |
| Inclusion criteria | Having had an LDD between 01/01/2010 and 30/06/2010 in one of the selected cancer sites; over 18 years old at the time of diagnosis. |
| Population type | |
| Age |
Adulthood (19 to 24 years) Adulthood (25 to 44 years) Adulthood (45 to 64 years) Elderly (65 to 79 years) Great age (80 years and more) |
| Population covered |
Sick population |
| Gender |
Male Woman |
| Geography area |
National |
| Detail of the geography area | Metropolitan France. |
| Data collection | |
| Dates | |
| Date of first collection (YYYY or MM/YYYY) | 03/2012 |
| Date of last collection (YYYY or MM/YYYY) | 03/2013 |
| Size of the database | |
| Size of the database (number of individuals) |
[1000-10 000[ individuals |
| Details of the number of individuals | 4,349 |
| Data | |
| Database activity |
Data collection completed |
| Type of data collected |
Clinical data Declarative data |
| Clinical data (detail) |
Direct physical measures |
| Details of collected clinical data | Baseline characteristics of cancer, healthcare consumption data, comorbidities, therapeutic treatment details. |
| Declarative data (detail) |
Paper self-questionnaire |
| Details of collected declarative data | Questionnaire administered to patients four 12 cancer sites: collection of sociodemographic data, data on discovery and disclosure of illness, treatment received, perceived side effects, fatigue (EORTC scale), quality of life (SF-12), pain (DN4 and ID-pain), daily and social life, employment and impact of illness on return to work, sexuality, fertility/parenting. |
| Presence of a biobank |
No |
| Health parameters studied |
Health event/morbidity Health event/mortality Health care consumption and services Quality of life/health perception |
| Care consumption (detail) |
Hospitalization Medical/paramedical consultation Medicines consumption |
| Procedures | |
| Data collection method | Data collection procedure: - Telephone interviews with respondents with possible self-administered questionnaires for sites in the upper aerodigestive tract and lungs. - Questionnaire survey to physicians treating patients. - Paired with SNIIR-AM healthcare consumption data. 3 types of data collection: - Cross-sectional survey by telephone/individual questionnaires - medical questionnaire survey to physicians treating patients - healthcare consumption data (SNIIR-AM). |
| Quality procedure(s) used | Consistency request after electronic data is recorded. |
| Participant monitoring |
No |
| Links to administrative sources |
Yes |
| Linked administrative sources (detail) | SNIIR-AM, PMSI. |
| Promotion and access | |
| Promotion | |
| Access | |
| Terms of data access (charter for data provision, format of data, availability delay) | Contact the scientist in charge. |
| Access to aggregated data |
Access on specific project only |
| Access to individual data |
Access on specific project only |
| ABOUT | CATALOG | RESOURCES | USEFUL LINKS |
This site complies with the HONcode standard for trustworthy health information: |
8 rue de la Croix Jarry 75013 Paris Phone : +33 1 44 23 67 47 |
Partners - FAQ - Contact - Site map - Legal notices - Administration - Updated on December 15 2020 - Version 4.10.05
