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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00247546
Other study ID # 02032002
Secondary ID
Status Completed
Phase N/A
First received November 1, 2005
Last updated October 17, 2006
Start date March 2003
Est. completion date March 2005

Study information

Verified date September 2006
Source The Hospital District of Satakunta
Contact n/a
Is FDA regulated No
Health authority Finland: Ministry of Social Affairs and Health
Study type Interventional

Clinical Trial Summary

The aim of this study is to describe and analyse the effects of multifactorial trial on the incidence of falls and injurious falls and on different risk factors of falling among the home-dwelling aged.


Description:

The aims of the study:

1. To implement a program for the prevention of falls and injurious falls.

2. To describe the structure and activities of the fall prevention program implemented among the aged who are living in their own home, have at least moderate cognitive abilities, have fallen during previous 12 months and are 65 years of age or older. A further aim is to describe the frequency of participation according to age, gender, residence, health and physical condition.

3. To describe the effects of prevention on primary risk factors of falling such as muscle strength, balance, eye sight, medications, depression and home hazards in relation to age, gender, health and physical condition.

4. To describe and assess the effects of prevention on the incidence of falls and injurious falls.

5. To assess the effects of prevention on physical, cognitive and psychosocial functional abilities, quality of life and use of health and social services and deaths.


Recruitment information / eligibility

Status Completed
Enrollment 592
Est. completion date March 2005
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 65 Years to 85 Years
Eligibility Inclusion Criteria:

- 65 years of age or older

- home-dweller

- having fallen at least once during the previous 12 months

- at least moderate cognitive abilities (MMSE over 17)

- able to walk 10 metres independently

Exclusion Criteria:

- MMSE under 17

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
Multifactorial prevention


Locations

Country Name City State
Finland The Hospital District of Satakunta Pori

Sponsors (1)

Lead Sponsor Collaborator
The Hospital District of Satakunta

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of falls and injurious falls
Secondary Risk factors of falling
Secondary Functional abilities
Secondary Quality of life
Secondary Use of health and social services
Secondary Deaths
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