Cardiovascular Function and Physical Activity in COVID-19 (CV-COVID)

August 30, 2023 updated by: Djordje Jakovljevic, Coventry University

Cardiovascular Implications and Physical Activity in Middle-age and Older People With a History of Coronavirus 2019 (COVID-19)

The purpose of this study is to a) assess how coronavirus 2019 (COVID-19) affects cardiac function in middle age and older adults and b) assess if a physical activity intervention (increased daily step count by 2,000) can affect cardiac function in a population with a history of COVID-19.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Cardiac function will be assessed by obtaining arterial stiffness, comprehensive echocardiography measurements and haemodynamic monitoring. Arterial stiffness will assess primarily pulse wave velocity (PWV) and echocardiography. Graded cardiopulmonary exercise stress testing coupled with non-invasive gas exchange and haemodynamic monitoring will also be performed. Physical activity will be assessed objectively using pedometers and accelerometry. Quality of life, sleep/ circadian rhythm, fatigue, anxiety and depression will be measured using the validated Short-Form-36 (SF-36) questionnaire, Pittsburgh Sleep scale (PSQI), Chalder fatigue (CF) scale and the Depression, Anxiety and Stress Scale (DASS-21).

Study Type

Interventional

Enrollment (Actual)

124

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United Kingdom
    • West Midlands
      • Coventry, West Midlands, United Kingdom, CV1 2DS
        • Coventry University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

50 years to 85 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Between 50-85 years old
  • Up to date with all COVID-19 vaccinations
  • COVID participants - had a positive test for COVID-19 over 28 days of initial visit but before 18 months. Non-COVID participants - never received a positive COVID-19 test result, and no symptoms during periods where testing was unavailable.

Exclusion Criteria:

  • Chronic respiratory and cardiovascular conditions i.e., chronic obstructive pulmonary disease (COPD), emphysema, pulmonary hypertension, coronary artery disease
  • Severe hypertension
  • Acute or chronic neurological impairment or progressive neurological disease
  • Use of medication known to directly affect cardiac function
  • Current smoker
  • Body mass index > 35 kg/m2
  • People who exceed current physical activity guidelines defined by the World Health Organization (WHO).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Non-COVID participants
Experimental: COVID participants in intervention
The intervention group will attend the laboratory for baseline testing and complete a week of usual daily activity. Following this week they will then be guided to increase their daily step count by 2,000 and supported through weekly telephone calls.
Behavioral: Active-at-home-HF
Increase daily step count by 2,000 and weekly telephone calls.
No Intervention: COVID participants assigned to usual daily activity

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Difference and change in left ventricular global longitudinal strain.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in left ventricular global longitudinal strain between COVID and non-COVID participants at rest and during peak exercise on baseline assessment.
  2. Change in left ventricular global longitudinal strain between COVID intervention and COVID usual care group at rest and during peak exercise on baseline and end of study assessments.

Left ventricular global longitudinal strain is measured as a percentage (%) using transthoracic echocardiography.
12 weeks (baseline to 12 weeks)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Difference and change in pulse wave velocity.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in pulse wave velocity between COVID and non-COVID participants at baseline assessment.
  2. Change in pulse wave velocity between COVID intervention and COVID usual care group at baseline and end of study assessments.

Pulse wave velocity (a measure of arterial stiffness) will be measured in meters per second (m/s) using a tonometer and sphygmomanometer.
12 weeks (baseline to 12 weeks)
Difference and change in augmentation index.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in augmentation index between COVID and non-COVID participants at baseline assessment.
  2. Change in augmentation index between COVID intervention and COVID usual care group at baseline and end of study assessments.

Augmentation index (a measure of arterial stiffness) will be measured as percentage (%) using sphygmomanometer.
12 weeks (baseline to 12 weeks)
Difference and change in resting cardiac output.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in resting cardiac output between COVID and non-COVID participants at baseline assessment.
  2. Change in resting cardiac output between COVID intervention and COVID usual care group at baseline and end of study assessments.

Cardiac output (i.e. volume of blood ejected from the heart) will be measured in litres per minute (L/min) using non-invasive monitoring technology.
12 weeks (baseline to 12 weeks)
Difference and change in maximal cardiac output.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in maximal cardiac output between COVID and non-COVID participants at baseline assessment.
  2. Change in maximal cardiac output between COVID intervention and COVID usual care group at baseline and end of study assessments.

Cardiac output (i.e. volume of blood ejected from the heart) will be measured in litres per minute (L/min) using non-invasive monitoring technology.
12 weeks (baseline to 12 weeks)
Difference and change in resting heart rate.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in resting heart rate between COVID and non-COVID participants at baseline assessment.
  2. Change in resting heart rate between COVID intervention and COVID usual care group at baseline and end of study assessments.

Heart rate (i.e. times the heart beats per minute) will be measured using non-invasive monitoring technology.
12 weeks (baseline to 12 weeks)
Difference and change in maximal heart rate.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in maximal heart rate between COVID and non-COVID participants at baseline assessment.
  2. Change in maximal heart rate between COVID intervention and COVID usual care group at baseline and end of study assessments.

Heart rate (i.e. times the heart beats per minute) will be measured using non-invasive monitoring technology.
12 weeks (baseline to 12 weeks)
Difference and change in resting stroke volume.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in resting stroke volume between COVID and non-COVID participants at baseline assessment.
  2. Change in resting stroke volume between COVID intervention and COVID usual care group at baseline and end of study assessments.

Stroke volume (i.e. volume of blood pumped out of the heart in one beat) will be measured in liters (L) using non-invasive monitoring technology.
12 weeks (baseline to 12 weeks)
Difference and change in maximal stroke volume.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in maximal stroke volume between COVID and non-COVID participants at baseline assessment.
  2. Change in maximal stroke volume between COVID intervention and COVID usual care group at baseline and end of study assessments.

Stroke volume (i.e. volume of blood pumped out of the heart in one beat) will be measured in liters (L) using non-invasive monitoring technology.
12 weeks (baseline to 12 weeks)
Difference and change in resting systemic vascular resistance.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in resting systemic vascular resistance between COVID and non-COVID participants at baseline assessment.
  2. Change in resting systemic vascular resistance between COVID intervention and COVID usual care group at baseline and end of study assessments.

Systemic vascular resistance (i.e. the force exerted on circulating blood by the vasculature of the body) will be measured in mmHg⋅min/mL using non-invasive monitoring technology.
12 weeks (baseline to 12 weeks)
Difference and change in maximal systemic vascular resistance.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in maximal systemic vascular resistance between COVID and non-COVID participants at baseline assessment.
  2. Change in maximal systemic vascular resistance between COVID intervention and COVID usual care group at baseline and end of study assessments.

Systemic vascular resistance (i.e. the force exerted on circulating blood by the vasculature of the body) will be measured in mmHg⋅min/mL using non-invasive monitoring technology.
12 weeks (baseline to 12 weeks)
Difference and change in maximal oxygen uptake (VO2 max).
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in VO2 max between COVID and non-COVID participants at baseline assessment.
  2. Change in VO2 max between COVID intervention and COVID usual care group at baseline and end of study assessments.

VO2 max (i.e. maximal oxygen uptake) will be measured in milliliters per minute (mL/min).
12 weeks (baseline to 12 weeks)
Difference and change in Forced Expiratory Volume 1 (FEV1)/ forced vital capacity (FVC) ratio.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in FEV/FEV1 ratio between COVID and non-COVID participants at baseline assessment.
  2. Change in FEV/FEV1 ratio between COVID intervention and COVID usual care group at baseline and end of study assessments.

FEV/FEV1 ratio (i.e. the ratio that reflects the amount of air you can forcefully exhale from your lungs) will be measured using spirometry.
12 weeks (baseline to 12 weeks)
Change in quality of life measured by the SF-36 questionnaire between baseline and post intervention assessment at 12 weeks.
Time Frame: 12 weeks (baseline to 12 weeks)
Difference in quality of life 36 Item Short Form survey scores between baseline and end of study assessments.Score ranges from 0-100, with higher scores associated with a better outcome.
12 weeks (baseline to 12 weeks)
Difference and change in depression, anxiety and stress measured on the DASS-21 questionnaire.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in depression, anxiety and stress between COVID and non-COVID participants at baseline assessment.
  2. Change in depression, anxiety and stress between COVID intervention and COVID usual care group at baseline and end of study assessments.

Depression, anxiety and stress measured on the DASS-21 questionnaire. Score ranges from 0-56, with higher scores associated with a worse outcome.
12 weeks (baseline to 12 weeks)
Difference and change in global sleep efficiency.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in global sleep efficiency between COVID and non-COVID participants at baseline assessment.
  2. Change in global sleep efficiency between COVID intervention and COVID usual care group at baseline and end of study assessments.

Sleep efficiency is measured on the Pittsburgh Sleep Quality Index (PSQI) questionnaire. Score ranges from 0-21, with higher scores associated with a worse outcome.
12 weeks (baseline to 12 weeks)
Change in sleep efficiency.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in sleep efficiency between COVID and non-COVID participants at baseline assessment.
  2. Change in sleep efficiency between COVID intervention and COVID usual care group at baseline and end of study assessments.

Sleep efficiency is measured using the Condor Actigraph watch. Score ranges from 0-100%, with higher scores associated with a higher sleep efficiency.
12 weeks (baseline to 12 weeks)
Difference and change in right ventricular global longitudinal strain.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in resting right ventricular global longitudinal strain between COVID and non-COVID participants at baseline assessment.
  2. Change in resting right ventricular global longitudinal strain between COVID intervention and COVID usual care group at baseline and end of study assessments.

Right ventricular global longitudinal strain is measured as a percentage (%) using transthoracic echocardiography.
12 weeks (baseline to 12 weeks)
Difference and change in left atrial strain.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in left atrial strain between COVID and non-COVID participants at rest and during exercise on baseline assessment.
  2. Change in left atrial strain between COVID intervention and COVID usual care group at rest and during exercise on baseline and end of study assessments.

Left atrial strain is measured as a percentage (%) using transthoracic echocardiography.
12 weeks (baseline to 12 weeks)
Difference and change in ventricular arterial coupling.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in ventricular arterial coupling between COVID and non-COVID participants on baseline assessment.
  2. Change in ventricular arterial coupling between COVID intervention and COVID usual care group on baseline and end of study assessments.

Ventricular arterial coupling (VAC) is a ratio which is calculated using the formula VAC = Ea/Ees; where Ea = arterial elastance (0.9 x systolic blood pressure/ stroke volume) and Ees = ventricular elastance (0.9 x systolic blood pressure/ left ventricular end systolic volume (LVESV).

stroke volume and LVESV are both calculated using echocardiography techniques.
12 weeks (baseline to 12 weeks)
Difference and change in right ventricular diastolic function.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in right ventricular diastolic function between COVID and non-COVID participants on baseline assessment.
  2. Change in right ventricular diastolic function between COVID intervention and COVID usual care group on baseline and end of study assessments.

Right ventricular diastolic function has no particular units, rather is graded impaired or restrictive right ventricular filling using several echocardiographic measurements i.e., tricuspid valve E:A ratio, tricuspid valve deceleration time (milliseconds (ms)).
12 weeks (baseline to 12 weeks)
Difference and change in electrocardiography (ECG) R-R interval average.
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in R-R average between COVID and non-COVID participants at rest on baseline assessment.
  2. Change in R-R average between COVID intervention and COVID usual care group at rest on baseline and end of study assessments.

R-R average is a measurement of Heart Rate Variability, measured in milliseconds (ms) using electrocardiography.
12 weeks (baseline to 12 weeks)
Difference and change in root mean square of successive ECG RR interval difference (RMSSD).
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in RMSSD between COVID and non-COVID participants at rest on baseline assessment.
  2. Change in RMSSD between COVID intervention and COVID usual care group at rest on baseline and end of study assessments.

RMSSD is a measurement of Heart Rate Variability, measured in milliseconds (ms) using electrocardiography.
12 weeks (baseline to 12 weeks)
Difference and change in Standard Deviation Normal RR Intervals (SDNN).
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in SDNN between COVID and non-COVID participants at rest on baseline assessment.
  2. Change in SDNN between COVID intervention and COVID usual care group at rest on baseline and end of study assessments.

SDNN is a measurement of Heart Rate Variability, measured in milliseconds (ms) using electrocardiography.
12 weeks (baseline to 12 weeks)
Difference and change in low-frequency power (LF).
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in LF between COVID and non-COVID participants at rest on baseline assessment.
  2. Change in LF between COVID intervention and COVID usual care group at rest on baseline and end of study assessments.

LF (absolute power) is a measurement of Heart Rate Variability, measured in milliseconds squared (ms2) using electrocardiography.
12 weeks (baseline to 12 weeks)
Difference and change in high-frequency power (HF).
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in HF between COVID and non-COVID participants at rest on baseline assessment.
  2. Change in HF between COVID intervention and COVID usual care group at rest on baseline and end of study assessments.

HF (absolute power) is a measurement of Heart Rate Variability, measured in milliseconds squared (ms2) using electrocardiography.
12 weeks (baseline to 12 weeks)
Difference and change in low-frequency power (LFnu).
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in LFnu between COVID and non-COVID participants at rest on baseline assessment.
  2. Change in LFnu between COVID intervention and COVID usual care group at rest on baseline and end of study assessments.

LFnu (relative power) is a measurement of Heart Rate Variability, measured in normal units using electrocardiography.
12 weeks (baseline to 12 weeks)
Difference and change in low-frequency power (HFnu).
Time Frame: 12 weeks (baseline to 12 weeks)
  1. Difference in HFnu between COVID and non-COVID participants at rest on baseline assessment.
  2. Change in HFnu between COVID intervention and COVID usual care group at rest on baseline and end of study assessments.

HFnu (relative power) is a measurement of Heart Rate Variability, measured in normal units using electrocardiography.
12 weeks (baseline to 12 weeks)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Coventry University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 7, 2022

Primary Completion (Actual)

May 11, 2023

Study Completion (Actual)

May 11, 2023

Study Registration Dates

First Submitted

August 3, 2022

First Submitted That Met QC Criteria

August 3, 2022

First Posted (Actual)

August 8, 2022

Study Record Updates

Last Update Posted (Estimated)

August 31, 2023

Last Update Submitted That Met QC Criteria

August 30, 2023

Last Verified

August 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • P125303

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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