An observational study in Impaired Health, Disease and Wellbeing, sponsored by Region Sjælland. Status unknown at 1 site in Denmark. Open to participants aged Up to 110 Years. Per ClinicalTrials.gov, last updated 2016-10-07.
Sponsored by Region Sjælland · Observational
The study is a epidemiological, cross-sectional study in a mainly rural area of Denmark in Denmark. Life expectancy is shorter, morbidity is higher, and social problems more prevalent than in the urban areas of the country. The population study aims at examining complexities of environmental, hereditary, lifestyle, and social factors as determinants and predisposing factors for morbidity, health, and quality of life. The study will cover physical, mental, and social dimensions and examine family patterns and subgroups. The study will provide baseline information for later follow-up.
1,740 studies on the registry are indexed under Mental Disorders; 348 are open to participants now.
This study's planned enrollment of 25,000 is above the median of 220 across 389 observational studies indexed under Mental Disorders.
Browse Mental Disorders studies →Region Sjælland is the lead sponsor of 3 studies on the registry; none are open to participants now.
Compared within Mental Disorders, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Disease. The counts are of registry records indexed under each term, refreshed daily. How we classify →
The population of Lolland and Guldborgsund municipalities in Denmark.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Health
Self-administered questionnaires, clinical examination, and biospecimen
Time frame: Cross-sectional, measured once
Morbidity
Self-administered questionnaires, clinical examination, and biospecimen
Time frame: Cross-sectional, measured once
Risk factors
Self-administered questionnaires, clinical examination, and biospecimen
Time frame: Cross-sectional, measured once
This study is status unknown, as verified in Jun 2016. You cannot join it, but the record below documents what was studied.
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Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.