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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT04140331
Other study ID # 19CH049
Secondary ID 2019-A00525-52
Status Terminated
Phase
First received
Last updated
Start date January 9, 2020
Est. completion date June 4, 2024

Study information

Verified date June 2024
Source Centre Hospitalier Universitaire de Saint Etienne
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Short term morbidity after elective cardiac surgery remains significant. Standard predictive models, considering simple patient demographics and clinical parameters, show limited efficiency in individual operative risk assessment. There is growing evidence about daily physical activity as a relevant indicator of preoperative "frailty". Although cardiopulmonary exercise testing remains a gold standard, we are looking for more simple tools in order to identify patients with poor physical condition. Accelerometry may be an objective and reproductible method to measure physical activity at patient's home.


Description:

The aim of this study is to compare accelerometer-assessed preoperative physical activity between two groups of patients with different postoperative length of stay following elective cardiac surgery. In the future, accelerometry could be used to identify patients that may benefit from prehabilitation programs including exercise therapy before elective cardiac surgery.


Recruitment information / eligibility

Status Terminated
Enrollment 202
Est. completion date June 4, 2024
Est. primary completion date April 2, 2024
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria: - Adult subject (= 60 years) awaiting elective cardiac surgery - Patients affiliated or entitled to a social security scheme - Patients who have received information about the study and have given their oral consent to participate Exclusion Criteria: - Pregnant woman, - Major limitations in physical activity for orthopedic or musculoskeletal reasons - Patients under judicial protection (curator or guardianship)

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Accelerometer
Patient will wear the accelerometer for 7 consecutive days to measure the level of physical activity.

Locations

Country Name City State
France Chu Saint-Etienne Saint-Étienne

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Saint Etienne

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mean daily preoperative walking activity (average of steps/day over a period of 7 days) Measured by accelerometry. Day: 7
Secondary Total energy expenditure evaluated over a 7 days (steps/day) Measured by accelerometry. Day: 7
Secondary Low activity time in hours per week (hours/week) Measured by accelerometry. Day: 7
Secondary Moderate activity time in hours per week (hours/week) Measured by accelerometry. Day: 7
Secondary Intense activity time in hours per week (hours/week) Measured by accelerometry. Day: 7
Secondary Time of very intense activity in hours per week (hours/week) Measured by accelerometry. Day: 7
Secondary Sleep time in hours per week (hours/week) Measured by accelerometry. Day: 7
Secondary Analysis of questionary Duke Activity Status Index (DASI) over a period of 7 days Questionary Duke Activity Status Index (DASI) estimates the maximum volume of oxygen used in one minute (VO2 Max) as well as its effort capacity in metabolic equivalent.
It contains 11 items. The higher the score indicates better functional capacity.
Day: 7
Secondary Analysis of questionary Short Nutritional Assessment Questionnaire (SNAQ) over a period of 7 days Questionary Short Nutritional Assessment Questionnaire (SNAQ) evaluates nutritional status. The higher the score indicates an important nutritional support. Day: 7
Secondary Dosage of albumin (g/L) Measured by blood sample. Day: 7
Secondary Dosage of prealbumin (g/L) Measured by blood sample. Day: 7
Secondary Preoperative strength assessed by dynamometry (Kg) Measured by Hand Grip test. Day: 14
Secondary Relationship between preoperative physical activity and duration of stay in intensive care Correlation between preoperative physical activity and duration of stay in intensive care. Months: 26
Secondary Preoperative clinical outcome and duration of stay in intensive care Correlation between preoperative clinical outcome and duration of stay in intensive care. Months: 26
Secondary Postoperative clinical outcome and duration of stay in intensive care Correlation between postoperative clinical outcome and duration of stay in intensive care. Months: 26
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