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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03420326
Other study ID # 201711083RIND
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 26, 2018
Est. completion date June 1, 2018

Study information

Verified date January 2018
Source National Taiwan University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Atrial fibrillation (AF) is the most common arrhythmias in clinical practice. Research investigating hospitalized patients have indicated there are deleterious effects of AF on patients besides the disease burden itself, including longer stay days for hospitalization, higher rates of frailty and increasing mortality rate after discharged in six months. In the community-dwelling research also found that elderly with AF have lower cognitive function, physical functional tests score and slower walking speed compared with the health ones. However, there is limited articles investigating the impact of AF on community-dwelling elderly, and the relationship between AF and frailty is also lack of discussion. According to the aged society and increasing prevalence of AF, the relationship between AF and frailty in community-dwelling elderly is warranting investigated.


Recruitment information / eligibility

Status Completed
Enrollment 256
Est. completion date June 1, 2018
Est. primary completion date June 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria:

- Older than 65 years old

Exclusion Criteria:

diagnosed with the following disease

1. Cardiovascular diseases: myocardial infarction, peripheral vascular diseases, aortic plaque

2. Cerebrovascular disease: stroke, transient ischemic attack, emboli

3. Heart failure

4. Participants who cannot finish the trial

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Frailty status assessment
The Edmonton frail scale and Frailty criteria by Dr. Fried would be used to assess participants frailty status

Locations

Country Name City State
Taiwan Ming-Ting Yang Taipei Zhongzheng District

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Frailty status Edmonton frail scale and Frailty criteria by Dr. Fried would be used to evaluate the frail status of the participants The frail status assessment would take about 10 minutes
Secondary Body composition Maltron BioScan BF-920, Essex, UK would be used to assess participants' body composition The body composition test would take about 10 minutes
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