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Health Status and Its Socio-economic Covariates of the Older Population in Poland - the Nationwide PolSenior2 Survey.

M

Medical University of Gdansk

Status

Unknown

Conditions

Aging Disorder
Frailty Syndrome
Behaviors, Health
Health Care Utilization
Age Problem
Immunity Disorders
Healthy Aging

Treatments

Other: medical history, blood and urine tests

Study type

Observational

Funder types

Other

Identifiers

NCT04026815
6/5/4.2/NPZ/2017/1203/1257

Details and patient eligibility

About

The PolSenior2 survey is aimed to characterise health status of old and very-old adults in Poland.

Full description

One of the goals is assessing the prevalence and control of age-related diseases and of the "geriatric giants" (immobility, instability, incontinence, sensory deficiency, cognition and mood disorders) which lead to frailty, disability and dependence. Monitoring of health status, health behaviors and identifying socio-economic factors favoring successful aging will be significant. As the polypragmasy and adverse drug reactions remain a significant issue in the geriatric care, pharmacotherapy and medical adherence will also be examined.

The additional purpose of the study is to evaluate the utilization and access to health care and social services in respect to needs for assistance and long-term care, as well as the level and different forms of these needs.

The project is planned as a cross-sectional survey of representative sample of 6000 people aged 60 years and over. The study protocol consists of questionnaires (medical, socio-economic, dietary), comprehensive geriatric assessment, anthropometric and blood pressure measurements and laboratory tests. The data are collected by well-trained nurses during three visits at respondents homes.

Enrollment

6,000 estimated patients

Sex

All

Ages

60+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • over 60 years of age,
  • randomly selected from database of all Polish citizens,
  • consent to participate in the study.

Exclusion criteria

  • under 60 years of age,
  • no consent to participate in the study.

Trial design

6,000 participants in 7 patient groups

60 - 65 years
Description:
Subjects were selected using a three stage stratified and proportional random sampling in seven equally size (n=850) age groups: 60-65, 65-69, 70-74, 75-79, 80-84, 85-89, 90+ years.
Treatment:
Other: medical history, blood and urine tests
65 - 69 years
Description:
Subjects were selected using a three stage stratified and proportional random sampling in seven equally size (n=850) age groups: 60-65, 65-69, 70-74, 75-79, 80-84, 85-89, 90+ years.
Treatment:
Other: medical history, blood and urine tests
70 - 74 years
Description:
Subjects were selected using a three stage stratified and proportional random sampling in seven equally size (n=850) age groups: 60-65, 65-69, 70-74, 75-79, 80-84, 85-89, 90+ years.
Treatment:
Other: medical history, blood and urine tests
75 - 79 years
Description:
Subjects were selected using a three stage stratified and proportional random sampling in seven equally size (n=850) age groups: 60-65, 65-69, 70-74, 75-79, 80-84, 85-89, 90+ years.
Treatment:
Other: medical history, blood and urine tests
80 - 84 years
Description:
Subjects were selected using a three stage stratified and proportional random sampling in seven equally size (n=850) age groups: 60-65, 65-69, 70-74, 75-79, 80-84, 85-89, 90+ years.
Treatment:
Other: medical history, blood and urine tests
85 - 89 years
Description:
Subjects were selected using a three stage stratified and proportional random sampling in seven equally size (n=850) age groups: 60-65, 65-69, 70-74, 75-79, 80-84, 85-89, 90+ years.
Treatment:
Other: medical history, blood and urine tests
≥90 years
Description:
Subjects were selected using a three stage stratified and proportional random sampling in seven equally size (n=850) age groups: 60-65, 65-69, 70-74, 75-79, 80-84, 85-89, 90+ years.
Treatment:
Other: medical history, blood and urine tests

Trial contacts and locations

1

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Central trial contact

Lukasz Wierucki, MD, PhD; Tomasz R. Zdrojewski, MD, Prof

Data sourced from clinicaltrials.gov

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