Health TrialsbyHealthPanel

Effect of Swimming Exercise on Diastolic Dysfunction

ConditionDiastolic Dysfunction
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age40-60
SponsorUşak University

About this trial

The aim of the study was to determine the rehabilitative effects of 12-week variable intensity swimming exercises on the cardiovascular system in women with diastolic dysfunction. Studies on how variable intensity swimming exercises contribute to the course of the disease in sedentary women with cardiovascular problems are limited. Previous studies generally consisted of studies on the effects of exercise applications on the cardiovascular system in different branches and their effects were determined.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

No echocardiographic abnormalities detected except for stage 1 diastolic dysfunction based on examinations conducted in the cardiology outpatient clinic,

Female gender,

Aged between 40 and 60 years as of the study initiation date,

No history of substance use, including smoking and alcohol,

Disqualifiers

Refusal to sign the informed consent form,

Failure to participate in at least one of the study measurements,

Inability to meet the necessary criteria for training and measurements,

Presence of illness or injury during training or measurements,

Trial design

Design model

Parallel

Treatments tested in this trial

  • Exercise

    Behavioral

    HIIT Group

Treatment groups

60 Participants
are divided into 3 treatment groups
Group A: HIIT GroupActive comparator 1 intervention
Group B: MICT GroupSham comparator 1 intervention
Group C: Non exercise GroupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Heart Rate Measurement by Electrocardiography

Heart rate will be measured using a GE Healthcare MAC 2000 ECG device after 10 minutes of rest. Unit of Measure: Beats per minute (bpm)

Time frame
6 months
2

P Wave Duration

The duration of the P wave will be measured using standard 12-lead ECG recordings. Unit of Measure: Milliseconds (ms)

Time frame
6 months
3

PR Interval

The PR interval will be measured using standard 12-lead ECG recordings. Unit of Measure: Milliseconds (ms)

Time frame
6 months
4

QRS Duration

The QRS duration will be measured using standard 12-lead ECG recordings. Unit of Measure: Milliseconds (ms)

Time frame
6 months

Secondary outcomes

1

Cardiac Cavity Dimensions by Echocardiography

Left ventricular internal diameter, left atrial size, and other cardiac cavity dimensions will be measured using Philips transthoracic echocardiography. Unit of Measure: Millimeters (mm)

Time frame
6 months
2

Interventricular Septal Thickness

Measurements of interventricular septal thickness at end-diastole will be taken using echocardiography. Unit of Measure: Millimeters (mm)

Time frame
6 months
3

Posterior Wall Thickness

Measurements of posterior wall thickness at end-diastole will be taken using echocardiography. Unit of Measure: Millimeters (mm)

Time frame
6 months
4

Systolic Function - Ejection Fraction

Left ventricular systolic function will be evaluated using ejection fraction (EF) by the modified Simpson method. Unit of Measure: Percentage (%)

Time frame
6 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Uşak University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: