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Swiss Study on Vitamin D and Calcium in Nursing Homes

University of Zurich (UZH) logo

University of Zurich (UZH)

Status

Completed

Conditions

Aging
Vitamin Deficiency

Treatments

Behavioral: peer physician-applied recommendation to the physicians

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Residents of nursing homes are endangered by malnutrition and vitamin D deficiency. Our study checks compliance with Swiss federal recommendations on vitamin D and calcium supplementation among residents of a Swiss nursing home. A peer physician-applied recommendation on compliance with the federal recommendations with individual evaluation of the residents will be sent to the physicians in care. After one year, data will be collected again.

Full description

The investigators plan to get a complete sample of all inhabitants, so the only inclusion criterion is to get an informed consent either from the residents or from their relatives. The following data will be recorded: Year of birth, gender, height, weight, blood pressure and heart rate, daily calcium intake from diet, nursing home scales on pain, depression, dementia and activities of daily life, date of entry to the home, diagnosis and medication lists. From a venous blood sample the investigators get: calcium, phosphate, albumin, creatinin, 25-hydroxyvitamin D, parathormone (intact).

Primary endpoint: Proportion of medication lists of residents complying with federal recommendation on vitamin D and calcium supplementation.

Secondary endpoints: 25-hydroxyvitamin D levels, effect of an intervention with a nursing home-applied recommendation to the physicians.

Enrollment

71 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Resident of nursing home on qualifying date
  • Written informed consent by residents or their relatives

Exclusion criteria

  • Refusion of participation

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

71 participants in 1 patient group

Entire group
Experimental group
Description:
A peer-applied guideline will be applied to the physicians.
Treatment:
Behavioral: peer physician-applied recommendation to the physicians

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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