Vitamin D3 - Omega3 - Home Exercise - HeALTHy Aging and Longevity Cohort

NCT ID: NCT05062018

Last Updated: 2022-12-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

534 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-11-26

Study Completion Date

2023-12-31

Brief Summary

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The DO-HEALTH trial will be extended into the cohort including the collection on life style factors such as diet, quality of life and physical activity, as well as health-related data on co-morbid conditions as well as a standardized assessment of multiple organ functions, physical, cognitive and mental function using surveys and standardized health assessments.

Detailed Description

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The DO-HEALTH cohort will be a continuation of the trial without intervention and will elucidate longterm determinants of healthy, active and independent aging in European community-dwelling older adults. The main emphasize of the cohort will be to determine the risk factors, to quantify the incidence and to describe the trajectories of incident frailty, impaired mobility, loss of independence and age related morbidity (e.g. heart arrhythmia, type 2 diabetes, falls, fractures).

Additionally, the cohort will continue to investigate the primary endpoints of the original trial like the risk and incidence of injurious falls (bone); functional decline (muscle); high blood pressure (cardiovascular); cognitive decline (brain); and the rate of any infection (immunity). Moreover, the cohort will include and extend key secondary and exploratory endpoints of the original trial such as incidence and prevalence of anemia, sarcopenia, cardiovascular diseases, type 2 diabetes and cancer.

Conditions

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Healthy Aging

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Former participation in the DO-HEALTH clinical trial study

Exclusion Criteria

* Inability or unwillingness to give written informed consent
* Medical condition that would make the results of the tests/assessments unreliable and/or would put too much burden to the participant, and/or leads to safety concerns.
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Heike Bischoff-Ferrari

OTHER

Sponsor Role lead

Responsible Party

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Heike Bischoff-Ferrari

Prof. Dr. med. DrPH

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Heike Bischoff-Ferrari, Prof. Dr. med. DrPH

Role: PRINCIPAL_INVESTIGATOR

University of Zurich

Locations

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Centre on Aging and Mobility, University of Zurich, City Hospital Zurich

Zurich, , Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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2019-00134

Identifier Type: -

Identifier Source: org_study_id

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