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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05553106
Other study ID # GO 20/299
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date September 23, 2022
Est. completion date November 2022

Study information

Verified date October 2022
Source Hacettepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The aim of our study is to evaluate cognitive status, kinesiophobia, physical activity level, and functional performance in coronary intensive care.


Description:

This study will be performed on patients who are hospitalized in the coronary intensive care unit, who can take simple commands, and whose condition is physiologically stable.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 10
Est. completion date November 2022
Est. primary completion date November 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Volunteering to participate in the research - Being under surveillance in the coronary intensive care unit Exclusion Criteria: - Presence of neurological disease that may affect the cognitive status - Not being clinically stable - Not to cooperate

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Turkey Hacettepe University Ankara

Sponsors (1)

Lead Sponsor Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Functional Performance Assessment Functional status score for the intensive care unit (FSS-ICU) will be used. 2 weeks
Secondary Symptom Assessment Cardiac symptom survey will be used. 2 weeks
Secondary Cognitive Status Assessment The Montreal Cognitive Assessment (MoCA) will be used 2 weeks
Secondary Physical Activity Level Physical activity level will be evaluated using the International Physical Activity Questionnaire - Short Form (IPAQ-SF). 2 weeks
Secondary Fear of Movement Fear of movement will be evaluated using the Fear of Activity in Patients with Coronary Artery Disease (Fact-CAD). 2 weeks
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