Effects of a Multidimensional Exercise Program on Cardiac Surgery Patients
Primary Purpose
Cardiac Surgery, Frailty
Status
Completed
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Multidimensional Exercise Program
Sponsored by
About this trial
This is an interventional supportive care trial for Cardiac Surgery focused on measuring Cardiac surgery, Frailty, Exercise program
Eligibility Criteria
Inclusion Criteria:
- 1.Aged above 40 and had received cardiac surgery. 2.Meet one of the Fried's phenotype of frailty. 3.Clear consciousness, can communicate with Chinese and Taiwanese. 4.Consent to join in this study.
Exclusion Criteria:
- 1.Bed-ridden or unable to perform activities of daily living independently. 2.Unstable illness condition. 3.Emergency condition. 4.Contraindications of performing exercise such as uncontrolled hypertension, uncontrolled arrhythmia.
Sites / Locations
- National Yang-Ming University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Multidimensional Exercise Program
Control group
Arm Description
Patients in this group will receive a 12 week exercise program including: (1) one 20-30 minute individual exercise consultation (teaching exercise which contain walking and resistance exercise by using elastic bands and elastic balls); (2) provided exercise booklet, exercise log, exercise video; (3) telephone follow-up once per week for 12 weeks.
Patients in this group maintain their daily life activities, and there is no intervention given.
Outcomes
Primary Outcome Measures
Changes in Fried's Phenotype of Frailty scores
Changes from baseline Fried's Phenotype of Frailty scores including five indicators: weight loss, exhaustion, weakness, slowness, and low physical activity, at 6 weeks, 12 weeks, 24 weeks. Each indicator was identified as positive and negative. Frailty was defined if more than 2 indicators were positive. Pre-frailty was defined if one indicator was positive.
Changes in symptoms distress scores
Changes from baseline symptoms distress scale at 6 weeks, 12 weeks, 24 weeks. Symptoms distress scale contains 17 common symptoms items, each item use Likert scale five point scoring, the total scores ranged from 17 to 85, the higher scores indicate worse symptom distress.
Secondary Outcome Measures
Changes in health related quality of life (SF-12) scores
Changes from baseline SF-12 divide into Physical Health Composite scale(PCS) and Mental Health composite scale(MCS), and the total scores ranged from 0 to 100, the higher scores indicate better quality of life at 6 weeks, 12 weeks, 24 weeks.
Changes in anxiety and depression scores
Changes from baseline hospital anxiety and depression scale at 6 weeks, 12 weeks, 24 weeks. The hospital anxiety and depression scale contains 14 questions(7 for assess anxiety and 7 for assess depression), each item use Likert scale four point scoring, the total scores ranged from 0 to 21, the higher scores indicate more severe anxiety and depression level.
Full Information
NCT ID
NCT04332887
First Posted
April 1, 2020
Last Updated
April 5, 2022
Sponsor
National Yang Ming University
1. Study Identification
Unique Protocol Identification Number
NCT04332887
Brief Title
Effects of a Multidimensional Exercise Program on Cardiac Surgery Patients
Official Title
Effects of a Multidimensional Exercise Program on Cardiac Surgery Patients
Study Type
Interventional
2. Study Status
Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
June 2, 2019 (Actual)
Primary Completion Date
March 11, 2021 (Actual)
Study Completion Date
March 11, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Yang Ming University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This RCT study aims to examine effects of a multidimensional exercise program in heart surgical patients. The following hypotheses were tested: patients who received the exercise program will report significant improvement in frailty, social support, anxiety and depression, quality of life after the 12-week program. Subjects are randomly assigned to the intervention or control group. Patients in the intervention group will receive a 12 week exercise program. Data are collected by physical indicators and a structural questionnaire to measure frailty, social support, anxiety and depression, quality of life, and nutritional assessment at baseline, 6 weeks, 12 weeks and 24 weeks after surgery.
Detailed Description
This study aims to develop multidimensional exercise program, and examine the effects of an exercise program in heart surgical patients. An experimental design is used. Subjects are selected using a purposeful sampling and are randomly assigned to the intervention or control group by using block size randomization method. Patients in the intervention group will receive a 12 week exercise program including: individual consultation, teaching exercise which contain walking and resistance exercise by using elastic bands and elastic balls. Data are collected by physical indicators and a structural questionnaire to measure frailty, quality of life, social support, anxiety and depression, symptom distress at baseline, 6 weeks, 12 weeks and 24 weeks after surgery . Data analysis includes descriptive statistics, Pearson correlation coefficient, independent t test, chi square, one way ANOVA and generalized estimating equation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Surgery, Frailty
Keywords
Cardiac surgery, Frailty, Exercise program
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients in the intervention group will receive a 12 week exercise program including: individual consultation, teaching exercise which contain walking and resistance exercise by using elastic bands and elastic balls.
Masking
Outcomes Assessor
Masking Description
One research assistant is trained for being a outcomes assessor in this study who did not know the allocation of participants.
Allocation
Randomized
Enrollment
91 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Multidimensional Exercise Program
Arm Type
Experimental
Arm Description
Patients in this group will receive a 12 week exercise program including: (1) one 20-30 minute individual exercise consultation (teaching exercise which contain walking and resistance exercise by using elastic bands and elastic balls); (2) provided exercise booklet, exercise log, exercise video; (3) telephone follow-up once per week for 12 weeks.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Patients in this group maintain their daily life activities, and there is no intervention given.
Intervention Type
Behavioral
Intervention Name(s)
Multidimensional Exercise Program
Intervention Description
Patients in experimental group will receive a 12 week exercise program; patients in control group maintain their usual life activities.
Primary Outcome Measure Information:
Title
Changes in Fried's Phenotype of Frailty scores
Description
Changes from baseline Fried's Phenotype of Frailty scores including five indicators: weight loss, exhaustion, weakness, slowness, and low physical activity, at 6 weeks, 12 weeks, 24 weeks. Each indicator was identified as positive and negative. Frailty was defined if more than 2 indicators were positive. Pre-frailty was defined if one indicator was positive.
Time Frame
baseline, 6week, 12 week, 24week
Title
Changes in symptoms distress scores
Description
Changes from baseline symptoms distress scale at 6 weeks, 12 weeks, 24 weeks. Symptoms distress scale contains 17 common symptoms items, each item use Likert scale five point scoring, the total scores ranged from 17 to 85, the higher scores indicate worse symptom distress.
Time Frame
baseline, 6week, 12 week, 24week
Secondary Outcome Measure Information:
Title
Changes in health related quality of life (SF-12) scores
Description
Changes from baseline SF-12 divide into Physical Health Composite scale(PCS) and Mental Health composite scale(MCS), and the total scores ranged from 0 to 100, the higher scores indicate better quality of life at 6 weeks, 12 weeks, 24 weeks.
Time Frame
baseline, 6 weeks, 12 weeks, 24 weeks
Title
Changes in anxiety and depression scores
Description
Changes from baseline hospital anxiety and depression scale at 6 weeks, 12 weeks, 24 weeks. The hospital anxiety and depression scale contains 14 questions(7 for assess anxiety and 7 for assess depression), each item use Likert scale four point scoring, the total scores ranged from 0 to 21, the higher scores indicate more severe anxiety and depression level.
Time Frame
baseline, 6 weeks, 12 weeks, 24 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
1.Aged above 40 and had received cardiac surgery. 2.Meet one of the Fried's phenotype of frailty. 3.Clear consciousness, can communicate with Chinese and Taiwanese. 4.Consent to join in this study.
Exclusion Criteria:
1.Bed-ridden or unable to perform activities of daily living independently. 2.Unstable illness condition. 3.Emergency condition. 4.Contraindications of performing exercise such as uncontrolled hypertension, uncontrolled arrhythmia.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ai-Fu Chiou, PhD
Organizational Affiliation
Professor
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Yang-Ming University
City
Taipei
ZIP/Postal Code
112
Country
Taiwan
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
21949560
Citation
Afilalo J. Frailty in Patients with Cardiovascular Disease: Why, When, and How to Measure. Curr Cardiovasc Risk Rep. 2011 Oct;5(5):467-472. doi: 10.1007/s12170-011-0186-0. Epub 2011 Aug 2.
Results Reference
background
PubMed Identifier
25440648
Citation
Akhtar S, Morris B, Roy R, Balogun SA. Case 3-2015: preventing adverse outcomes in the very elderly cardiac surgical patients. J Cardiothorac Vasc Anesth. 2015 Apr;29(2):510-21. doi: 10.1053/j.jvca.2014.07.014. Epub 2014 Oct 25. No abstract available. Erratum In: J Cardiothorac Vasc Anesth. 2015 Aug;29(4):e37. Morris, Benjamin [added]; Roy, Raymond [added]; Balogun, Seki A [added].
Results Reference
background
PubMed Identifier
26626157
Citation
de Labra C, Guimaraes-Pinheiro C, Maseda A, Lorenzo T, Millan-Calenti JC. Effects of physical exercise interventions in frail older adults: a systematic review of randomized controlled trials. BMC Geriatr. 2015 Dec 2;15:154. doi: 10.1186/s12877-015-0155-4.
Results Reference
background
PubMed Identifier
11253156
Citation
Fried LP, Tangen CM, Walston J, Newman AB, Hirsch C, Gottdiener J, Seeman T, Tracy R, Kop WJ, Burke G, McBurnie MA; Cardiovascular Health Study Collaborative Research Group. Frailty in older adults: evidence for a phenotype. J Gerontol A Biol Sci Med Sci. 2001 Mar;56(3):M146-56. doi: 10.1093/gerona/56.3.m146.
Results Reference
background
PubMed Identifier
12362007
Citation
Gill TM, Baker DI, Gottschalk M, Peduzzi PN, Allore H, Byers A. A program to prevent functional decline in physically frail, elderly persons who live at home. N Engl J Med. 2002 Oct 3;347(14):1068-74. doi: 10.1056/NEJMoa020423.
Results Reference
background
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Effects of a Multidimensional Exercise Program on Cardiac Surgery Patients
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