NCC is a unique infrastructure of prospective cohort studies in the Netherlands with a focus on collection, harmonization and pooling of extensive data to address multimorbidity. Through NCC researchers will have access to a diversity of data concerning mental health, physical health, social networks, stress, life style, environment, socio-demographic and economic factors. We aim to include all population-based and population-representative Dutch cohort studies that provide advanced longitudinal clinical phenotyping and biomedical data for research into the determinants of multimorbidity. NCC brings data and researchers together to perform excellent research into unraveling the complex interplay between biological mechanisms, lifestyle, behavioral, socio-economic and environmental factors. Linkage with CBS-data, PALGA, NKR and other registries will even further strengthen the possibilities for excellent multidisciplinary research
WebsiteNetwork detailsCatalogueLRGP
Leidsche Rijn Health Project
Description
The Leidsche Rijn Health Project is an ongoing study of the health and health trends of residents in the Leidsche Rijn neighborhood in Utrecht. The five primary care practices of the Leidsche Rijn Julius Health Centers are participating in this project. Through early 2021, every patient registered at one of the five primary care practices was invited to participate in the LRGP. Informed consent was obtained from participants upon enrollment. Participants were asked to complete questionnaires (general characteristics, lifestyle, female reproductive health questionnaire, medical history, medication use, quality of life, stress, etc.); blood samples were collected; height, weight, and blood pressure were measured; and, in certain cases, an ECG and/or spirometry were performed. Enrollment was completed in early 2021. Follow-up data is still being collected through a continuous link to the data recorded by the primary care physician in the medical record.
General Design
- Type
- Biobank, Cohort study
- Cohort type
- Population cohort
- Data collection type
- Retrospective
- Design
- Longitudinal
- Start/End data collection
- 1999 (ongoing)
- PID
- https://doi.org/10.71739/q16q-rk81
Population
- Countries
- Netherlands (the)
- Regions
- Utrecht
- Number of participants
- 12500
- Population age groups
- Adult (18+ years)
- Main medical condition
- No main medical condition
- Other inclusion criteria
- patient at participating GP practice
- Other exclusion criteria
- none
Organisations
Lead organisations
- University Medical Center Utrecht (UMC)
Julius CenterNetherlands (the)https://www.umcutrecht.nl
Contributors
Available Data & Samples
Data categories
- Survey data
- Physiological/Biochemical measurements
Sample categories
- Blood
- Blood (whole)
- Blood Buffy Coat
- Plasma
- Serum
Areas of information
- Socio-demographic and economic characteristics
- Socio-demographic
- Age/birthdate
- Sex/gender
- Marital/partner status
- Family and household structure
- Education
- Residence
- Labour force and retirement
- Job history
- Income, possessions, and benefits
- Lifestyle and behaviours
- Toxic Habits - Tobacco, Alcohol, Drugs
- Tobacco
- Alcohol
- Drugs
- Nutrition
- Physical activity
- Sleep
- Birth, pregnancy and reproductive health history
- Puberty, menstruation, menopause and andropause
- Contraception
- Pregnancy, delivery and birth
- Birth outcomes
- Fertility and sexual health
- Other reproductive health-related information
- Perception of health, quality of life, development and functional limitations
- Perception of health
- Quality of life
- Functional limitations
- Family Health History
- Parental diseases
- Systolic blood pressure
- Diastolic blood pressure
- Medication and supplements
- Medication and supplement intake
- Physical measures and assessments
- Anthropometry
- Laboratory measures
- Hematology
- Biochemistry
- Cognition, personality and psychological measures and assessments
- Psychological distress and emotions
- Social environment and relationships
- Social network
- Social participation
- Social support
Subpopulations
List of subpopulations for this resource
| Name | Description | Number of participants | |
|---|---|---|---|
No results for current selection |
Collection events
List of collection events defined for this resource
| Name | Description | Participants | Start end year | |
|---|---|---|---|---|
No results for current selection |
Networks
Part of networks
Publications
Access conditions
- Data access conditions
- health or medical or biomedical research
- Data use conditions
- research specific restrictions
- not for profit, non commercial use only
- publication required
- collaboration required
- geographical restriction
- publication moratorium
- time limit on use
- user specific restriction
- project specific restriction
- institution specific restriction
- return to database or resource
- Data access fee
- true
- Release type
- Other release type
- Prelinked
- true
- Linkage options
- Data is linked with JHN. Follow-up of LRGP participants can be retrieved form JHN.