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Bedside Cycling Exercises Post Heart Valve Surgeries

Primary Purpose

Heart Valve Diseases

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Bedside cycling
control
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Valve Diseases

Eligibility Criteria

20 Years - 40 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Fifty patients with valvular heart disease (VHD)who have undergone valve surgical intervention Their age between 20-40 years old. Both genders Exclusion Criteria: Cognitive impairment. Neurological disorders. Sever Musculoskeletal disorders (MSD) e.g. (late stages of osteoarthritis). Underlying pulmonary diseases (aspiration pneumonia, chronic obstructive pulmonary disease, pneumothorax, etc). Presence of comorbidities like: Liver disease e.g. Active cirrhosis or history of previous liver transplant. Renal disease e.g. Chronic renal disease, Renal failure. Complicated operative course: post-operative complication: a) Presence of preoperative cofounder complication: pulmonary hypertension (Pulmonary artery pressure) = which estimated by right ventricular systolic pressure (RVSP) is greater than 50 mmHg, left ventricular dysfunction which estimated left ventricular ejection fraction equals 40 % or less. b) Patients with Coronary artery bypass surgery, active infective endocarditis, acute valve dysfunction and other acute urgent conditions.

Sites / Locations

  • National Heart Institute (NHI)

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Bedside cycling Group

Routine physical therapy Group

Arm Description

Participants (25 patients) that will receive bedside cycling: Intensity: RPE from 11 to 13 (scale 6-20) Resting HR + 20-30 bpm (up to tolerance if non-symptomatic), from low intensity and progressed to medium intensity. Duration: Session duration: Total duration of 20 min, early morning. Frequency: once daily from medically stable until discharge. in addition the medical treatment and routinely physiotherapy protocol.

participant that will receive only routine physiotherapy treatment protocol and the medical treatment.

Outcomes

Primary Outcome Measures

Functional capacity
measured by Six Minutes Walk Test, it will be performed on a flat surface, with a predetermined distance 30 meters measured and marked off. Patients will be asked to walk self-paced back and forth between the 2 marked points for 6 minutes. Rests are allowed, and administrators are able to provide standardized feedback during and at the end of the test, The laps are counted, and a distance walked in 6 minutes is determined.
Functional capacity
measured by Six Minutes Walk Test, it will be performed on a flat surface, with a predetermined distance 30 meters measured and marked off. Patients will be asked to walk self-paced back and forth between the 2 marked points for 6 minutes. Rests are allowed, and administrators are able to provide standardized feedback during and at the end of the test, The laps are counted, and a distance walked in 6 minutes is determined.
Forced Vital Capacity
measured by Spirometry Pulmonary function test, (THOR laboratory Spiro Tube PC Spirometer) will assess Forced Vital Capacity (FCV) in liters.
Forced Vital Capacity
measured by Spirometry Pulmonary function test, (THOR laboratory Spiro Tube PC Spirometer) will assess Forced Vital Capacity (FCV) in liters.
Psychological status
The Depression Anxiety Stress Scales 42 were used to measure three negative emotional states (depression, anxiety, and stress) experienced by the patients in the previous week. A higher score on the scale indicates a more severe condition, with the highest possible score being 126 and the lowest score being 0.
Psychological status
The Depression Anxiety Stress Scales 42 were used to measure three negative emotional states (depression, anxiety, and stress) experienced by the patients in the previous week. A higher score on the scale indicates a more severe condition, with the highest possible score being 126 and the lowest score being 0.
Activities of Daily Living and Functional level
measuring Activities of Daily Living and Function level by using Barthel Index, the current level of 10 items the maximum score is 100, the lower scores ranging from 0- 20 indicating increased disability.
Activities of Daily Living and Functional level
measuring Activities of Daily Living and Function level by using Barthel Index, the current level of 10 items the maximum score is 100, the lower scores ranging from 0- 20 indicating increased disability.
the Quality of Life
The Short Form-12 Health Questionnaire was used to measure the Quality of Life over the past 4 weeks, consisting of two components: physical and mental. The highest possible score for the mental component was 60.75781, indicating a better mental condition. Similarly, the highest possible score for the physical component was 56.577706, indicating a better physical condition.
Length of hospital stay
compare the intervention group to control group length of hospital stay.

Secondary Outcome Measures

Functional Capacity
measured by Six Minutes Walk Test (6MWT), it will be performed on a flat surface, with a predetermined distance 30 meters measured and marked off. Patients will be asked to walk self-paced back and forth between the 2 marked points for 6 minutes. Rests are allowed, and administrators are able to provide standardized feedback during and at the end of the test, The laps are counted, and a distance walked in 6 minutes is determined.
Psychological status
The Depression Anxiety Stress Scales 42 were used to measure three negative emotional states (depression, anxiety, and stress) experienced by the patients in the previous week. A higher score on the scale indicates a more severe condition, with the highest possible score being 126 and the lowest score being 0.
the Quality of Life
The Short Form-12 Health Questionnaire was used to measure the Quality of Life over the past 4 weeks, consisting of two components: physical and mental. The highest possible score for the mental component was 60.75781, indicating a better mental condition. Similarly, the highest possible score for the physical component was 56.577706, indicating a better physical condition.
Incidence of adverse event
the potential incidence of adverse events in both groups will be reported during the study.
Prothrombin International Normalized Ratio (INR)
Prothrombin International Normalized Ratio (INR) in the Coagulation profile in both groups will be assessed and provided at one-month follow-up.

Full Information

First Posted
April 21, 2023
Last Updated
September 1, 2023
Sponsor
Cairo University
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1. Study Identification

Unique Protocol Identification Number
NCT05893433
Brief Title
Bedside Cycling Exercises Post Heart Valve Surgeries
Official Title
Effect of Early Bedside Cycling Exercises on Selected Physical and Psychological Outcomes in Patients After Heart Valve Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
January 1, 2023 (Actual)
Primary Completion Date
June 20, 2023 (Actual)
Study Completion Date
June 20, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The aim of this clinical trial is to assess the effect of early bedside cycling exercises post heart valve surgeries. the main question aims to answer: whether adding an early bedside cycling exercise will have an effect on patient's functional capacity, other physical outcomes and have an effect on patient's psychological state? The participant will be assessed blindly the physical and psychological outcomes before getting randomly allocated in groups. the bedside cycling will be introduced and conducted in the intervention group in addition to the conventional physical therapy cardiac rehabilitation routine through preexisted physical therapy staff who present the hospital: The routine use of breathing exercises, coughing techniques, chest wall vibrations, and mobilization is common during the first postoperative days. On the other hand, the control group will only receive the conventional rehabilitation, subsequently, both groups will be assessed and compared by addressing the difference of the outcomes before discharging from the hospital.
Detailed Description
The aim of the study is to assess the effect of early bedside cycling exercises on selected physical and psychological outcomes in patients after heart valve surgery. This study will be carried out on fifty patients diagnosed with valve heart disease and undergoing valve replacement or intervention. They will be recruited from National Heart Institute-Cairo, Egypt. The purpose, nature and the risk of the study will be explained to the patients and each patient will be consented prior to participation in the study. The patients in this study will randomly be assigned and randomly allocated into two equal groups (n=25), the intervention group will be treated daily from being extubated and being relatively stable until discharge from the hospital: Study group (25 patients): will receive bedside cycling in addition to the medical treatment and physiotherapy protocol. Control group (25 patients): will receive only routine physiotherapy treatment protocol and the medical treatment. The bedside cycling will be introduced and conducted in the intervention group in addition to the conventional phase one of cardiac rehabilitation program through preexisted physical therapy staff who present the hospital. Bedside cycling: once the patient is relatively stable by weaning off the ventilator and off the require inotropic support and continued until the discharge from the hospital. Intensity: Rating of Perceived exertion scale (RPE) from 11 to 13 (scale 6-20) post-surgery: resting HR + 20-30 bpm (up to tolerance if non-symptomatic), from low intensity and progressed to medium intensity (According to The American College of Sports Medicine (ASCM) recommendations for prescription of the exercises in phase one of cardiac rehabilitation). Duration: Session duration: Total duration of 20 min, early morning. Intervention duration: 5-15 Resting as the patient wishes and in case signs of exertion. Warming up for 5min: low impact, dynamic movement of large group of muscles through available Active Range of Motion (ROM) or introduce to cycling, HR after warming up 10-11 RPE Cooling down for 5 min or longer: patient observed 30 min after exercise to get to Resting Heart Rate (RHR) Guided by 11-13 RPE, talk test, 20-30 bpm above RHR (Target HR) and sign and symptoms for stopping exercise. According ASCM recommendations for prescription of the exercises in phase one of cardiac rehabilitation. Frequency: once daily from medically stable until discharge. Progression if the following conditions are reached: Initially increase the duration by up to15 min of low exercise time and then increase the intensity after the patient can complete 15- 20 min. Complete 15min with a medially stable condition Precaution: Vital signs before after and within range Avoid Valsalva maneuver. On the other hand, the control group will only receive the conventional rehabilitation routine: The routine use of breathing exercises, coughing techniques, chest wall vibrations, and mobilization is common during the first postoperative days. Subsequently, both groups will be assessed and compared by addressing the difference of the outcomes before discharging from the hospital.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Valve Diseases

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Masking Description
Patient are masked through out the study and health care providers who provide routine care of the patient whether are nurses, physicians or existed physiotherapist are also masked
Allocation
Randomized
Enrollment
41 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Bedside cycling Group
Arm Type
Experimental
Arm Description
Participants (25 patients) that will receive bedside cycling: Intensity: RPE from 11 to 13 (scale 6-20) Resting HR + 20-30 bpm (up to tolerance if non-symptomatic), from low intensity and progressed to medium intensity. Duration: Session duration: Total duration of 20 min, early morning. Frequency: once daily from medically stable until discharge. in addition the medical treatment and routinely physiotherapy protocol.
Arm Title
Routine physical therapy Group
Arm Type
Placebo Comparator
Arm Description
participant that will receive only routine physiotherapy treatment protocol and the medical treatment.
Intervention Type
Device
Intervention Name(s)
Bedside cycling
Intervention Description
participants receive daily cycling once the patient is relatively stable by weaning off the ventilator and off the require inotropic support and continued to the discharge from the hospital. Duration progression if the following conditions are reached: Initially increase the duration by up to15 min of low exercise time and then increase the intensity after the patient can complete 15- 20 min. Complete 15min with a medially stable condition gradually until reaching 20 minutes besides the routine physical therapy protocol of breathing exercises, coughing techniques, chest wall vibrations, and mobilization is common during the first postoperative days, The two most frequently used breathing techniques were deep breathing exercises and incentive spirometry and the medical treatment.
Intervention Type
Other
Intervention Name(s)
control
Intervention Description
the routine physical therapy protocol of breathing exercises, coughing techniques, chest wall vibrations, and mobilization is common during the first postoperative days, The two most frequently used breathing techniques were deep breathing exercises and incentive spirometry and the medical treatment.
Primary Outcome Measure Information:
Title
Functional capacity
Description
measured by Six Minutes Walk Test, it will be performed on a flat surface, with a predetermined distance 30 meters measured and marked off. Patients will be asked to walk self-paced back and forth between the 2 marked points for 6 minutes. Rests are allowed, and administrators are able to provide standardized feedback during and at the end of the test, The laps are counted, and a distance walked in 6 minutes is determined.
Time Frame
from the date of patient admission to the hospital until date of the surgical operation, an average of 2 weeks.
Title
Functional capacity
Description
measured by Six Minutes Walk Test, it will be performed on a flat surface, with a predetermined distance 30 meters measured and marked off. Patients will be asked to walk self-paced back and forth between the 2 marked points for 6 minutes. Rests are allowed, and administrators are able to provide standardized feedback during and at the end of the test, The laps are counted, and a distance walked in 6 minutes is determined.
Time Frame
through study completion, an average of 2 weeks.
Title
Forced Vital Capacity
Description
measured by Spirometry Pulmonary function test, (THOR laboratory Spiro Tube PC Spirometer) will assess Forced Vital Capacity (FCV) in liters.
Time Frame
from the date of patient admission to the hospital until date of the surgical operation, an average of 2 weeks.
Title
Forced Vital Capacity
Description
measured by Spirometry Pulmonary function test, (THOR laboratory Spiro Tube PC Spirometer) will assess Forced Vital Capacity (FCV) in liters.
Time Frame
through study completion, an average of 2 weeks.
Title
Psychological status
Description
The Depression Anxiety Stress Scales 42 were used to measure three negative emotional states (depression, anxiety, and stress) experienced by the patients in the previous week. A higher score on the scale indicates a more severe condition, with the highest possible score being 126 and the lowest score being 0.
Time Frame
from the date of patient admission to the hospital until date of the surgical operation, an average of 2 weeks.
Title
Psychological status
Description
The Depression Anxiety Stress Scales 42 were used to measure three negative emotional states (depression, anxiety, and stress) experienced by the patients in the previous week. A higher score on the scale indicates a more severe condition, with the highest possible score being 126 and the lowest score being 0.
Time Frame
through study completion, an average of 2 weeks.
Title
Activities of Daily Living and Functional level
Description
measuring Activities of Daily Living and Function level by using Barthel Index, the current level of 10 items the maximum score is 100, the lower scores ranging from 0- 20 indicating increased disability.
Time Frame
within the first 24-hour post-surgery
Title
Activities of Daily Living and Functional level
Description
measuring Activities of Daily Living and Function level by using Barthel Index, the current level of 10 items the maximum score is 100, the lower scores ranging from 0- 20 indicating increased disability.
Time Frame
through study completion, an average 7 days
Title
the Quality of Life
Description
The Short Form-12 Health Questionnaire was used to measure the Quality of Life over the past 4 weeks, consisting of two components: physical and mental. The highest possible score for the mental component was 60.75781, indicating a better mental condition. Similarly, the highest possible score for the physical component was 56.577706, indicating a better physical condition.
Time Frame
from the date of patient admission to the hospital until date of the surgical operation, an average of 2 weeks.
Title
Length of hospital stay
Description
compare the intervention group to control group length of hospital stay.
Time Frame
through study completion, an average of 2 weeks.
Secondary Outcome Measure Information:
Title
Functional Capacity
Description
measured by Six Minutes Walk Test (6MWT), it will be performed on a flat surface, with a predetermined distance 30 meters measured and marked off. Patients will be asked to walk self-paced back and forth between the 2 marked points for 6 minutes. Rests are allowed, and administrators are able to provide standardized feedback during and at the end of the test, The laps are counted, and a distance walked in 6 minutes is determined.
Time Frame
1 month follow-up.
Title
Psychological status
Description
The Depression Anxiety Stress Scales 42 were used to measure three negative emotional states (depression, anxiety, and stress) experienced by the patients in the previous week. A higher score on the scale indicates a more severe condition, with the highest possible score being 126 and the lowest score being 0.
Time Frame
1 month follow-up.
Title
the Quality of Life
Description
The Short Form-12 Health Questionnaire was used to measure the Quality of Life over the past 4 weeks, consisting of two components: physical and mental. The highest possible score for the mental component was 60.75781, indicating a better mental condition. Similarly, the highest possible score for the physical component was 56.577706, indicating a better physical condition.
Time Frame
1 month follow-up.
Title
Incidence of adverse event
Description
the potential incidence of adverse events in both groups will be reported during the study.
Time Frame
from the date of beginning cycling intervention or routinely physiotherapy until the date of discharge and will be assessed up to one month.
Title
Prothrombin International Normalized Ratio (INR)
Description
Prothrombin International Normalized Ratio (INR) in the Coagulation profile in both groups will be assessed and provided at one-month follow-up.
Time Frame
1 month follow-up.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Fifty patients with valvular heart disease (VHD)who have undergone valve surgical intervention Their age between 20-40 years old. Both genders Exclusion Criteria: Cognitive impairment. Neurological disorders. Sever Musculoskeletal disorders (MSD) e.g. (late stages of osteoarthritis). Underlying pulmonary diseases (aspiration pneumonia, chronic obstructive pulmonary disease, pneumothorax, etc). Presence of comorbidities like: Liver disease e.g. Active cirrhosis or history of previous liver transplant. Renal disease e.g. Chronic renal disease, Renal failure. Complicated operative course: post-operative complication: a) Presence of preoperative cofounder complication: pulmonary hypertension (Pulmonary artery pressure) = which estimated by right ventricular systolic pressure (RVSP) is greater than 50 mmHg, left ventricular dysfunction which estimated left ventricular ejection fraction equals 40 % or less. b) Patients with Coronary artery bypass surgery, active infective endocarditis, acute valve dysfunction and other acute urgent conditions.
Facility Information:
Facility Name
National Heart Institute (NHI)
City
Giza
ZIP/Postal Code
12651
Country
Egypt

12. IPD Sharing Statement

Learn more about this trial

Bedside Cycling Exercises Post Heart Valve Surgeries

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