Effect of Whey Protein' Supplementation and Exercise in Patients With Heart Failure (PROT-HF)
Primary Purpose
Heart Failure, Sarcopenia, Muscle Loss
Status
Unknown status
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
whey protein
Sponsored by
About this trial
This is an interventional other trial for Heart Failure focused on measuring heart failure, cardiac reabilitation, nutritional status, quality of life, milk protein
Eligibility Criteria
Inclusion Criteria:
- Clinical diagnosis of heart failure NYHA I or II after medical evaluation;
- Indication to participate in a cardiac rehabilitation program;
- Fully medicated for heart disease;
- Age greater than or equal to 50 years;
- Ejection fraction less than 50%.
Exclusion Criteria:
- Neoplasia at any site;
- Impaired renal function (<50ml / min / 1.73m2);
- Impaired hepatic function (TGP> 150U / l) or decompensated hepatic cirrhosis classified with Child-Pugh B or C;
- Presence of ressincronizer or other device;
- Atrial fibrilation;
- Allergy of milk protein.
Sites / Locations
- Elisa Maia dos Santos
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
whey protein
placebo group
Arm Description
The whey protein group will receive whey protein supplementation 30g/day of whey protein during three months (12 weeks)
The placebo group (maltodextrin) will receive 30g/day of maltodextrin during three months (12 weeks)
Outcomes
Primary Outcome Measures
Preservation of skeletal muscle mass
Assessment of body composition through bioelectrical impedance and anthropometry
Secondary Outcome Measures
Quality of life
Evaluation of health-related quality of life through the application of the Minnesota Living With Heart Failure Questionnaire validated for brazilian population
Muscle strength
Evaluation of manual gripping force through dynamometry
Change in peak oxygen uptake (VO2 peak)
Cardiopulmonary exercise test will be performed to measure VO2 peak and other parameters representative of cardiovascular reserve.
Microvascular reactivity
A laser speckle contrast imaging system with a laser wavelength of 785 nm (PeriCam PSI system, Perimed, Järfälla, Sweden) coupled to iontophoresis of acetylcholine and sodium nitroprusside will measure non-invasively real time cutaneous microvascular flow changes in the forearm. For the post occlusive reactive hyperemia (PORH) test, arterial occlusion will be performed with suprasystolic pressure (50 mmHg above the systolic arterial pressure) using a sphygmomanometer applied to the arm of the subject over three minutes. Peak skin flow will be measured after pressure release.
Full Information
NCT ID
NCT03142399
First Posted
May 3, 2017
Last Updated
December 10, 2017
Sponsor
National Institute of Cardiology, Laranjeiras, Brazil
1. Study Identification
Unique Protocol Identification Number
NCT03142399
Brief Title
Effect of Whey Protein' Supplementation and Exercise in Patients With Heart Failure
Acronym
PROT-HF
Official Title
Effect of Supplementation With Whey Protein in Preservation of Muscle Mass and Strength, Quality of Life of Patients With Heart Failure in Cardiac Rehabilitation
Study Type
Interventional
2. Study Status
Record Verification Date
December 2017
Overall Recruitment Status
Unknown status
Study Start Date
January 2, 2018 (Anticipated)
Primary Completion Date
December 30, 2018 (Anticipated)
Study Completion Date
June 30, 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Institute of Cardiology, Laranjeiras, Brazil
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
The aim of this study is evaluate the effect of whey protein supplementation on muscle mass preservation, improvement of strength and quality of life, and inflammatory parameters in patients with heart failure NYHA I or II followed by a cardiac rehabilitation program.
Detailed Description
Heart failure is the final route of most heart diseases and is a worldwide problem due to its high prevalence, morbidity and mortality. In Brazil, it is an important cause of hospitalization and one of the most important health challenges, since its prevalence tends to increase with the aging of the population and the increase in the survival of patients who have suffered acute coronary events. This is an ongoing epidemic problem, resulting in a high socioeconomic cost, represented by the expense of medications, repeated hospitalizations, loss of productivity, early retirements, possible surgeries and, ultimately, heart transplantation. In this sense, it is of great importance to carry out studies that evaluate the possible benefits of new clinical and nutritional interventions for HF patients, favoring the development of treatment strategies for these individuals and also for public health.
Our hypothesis is based on the fact that whey protein supplementation associated with physical exercise in patients with heart failure could promote preservation of muscle mass, increase in muscle strength, and improve quality of life, Body composition and physical capacity. The volunteers will receive 30 grams per day of whey protein or maltodextrin in a double-blind, controlled clinical trial lasting 12 weeks. During this period they will perform supervised physical exercise 3 times a week in a cardiac rehabilitation program. They will also receive nutritional counseling.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Sarcopenia, Muscle Loss, Quality of Life
Keywords
heart failure, cardiac reabilitation, nutritional status, quality of life, milk protein
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
4 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
whey protein
Arm Type
Experimental
Arm Description
The whey protein group will receive whey protein supplementation 30g/day of whey protein during three months (12 weeks)
Arm Title
placebo group
Arm Type
Placebo Comparator
Arm Description
The placebo group (maltodextrin) will receive 30g/day of maltodextrin during three months (12 weeks)
Intervention Type
Dietary Supplement
Intervention Name(s)
whey protein
Other Intervention Name(s)
supplementation with milk protein
Intervention Description
Supplementation with whey protein isolate or maltodextrin (30 grams per day) for 12 weeks associated with supervised exercise and nutritional counseling in patients with heart failure.
Primary Outcome Measure Information:
Title
Preservation of skeletal muscle mass
Description
Assessment of body composition through bioelectrical impedance and anthropometry
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Quality of life
Description
Evaluation of health-related quality of life through the application of the Minnesota Living With Heart Failure Questionnaire validated for brazilian population
Time Frame
12 weeks
Title
Muscle strength
Description
Evaluation of manual gripping force through dynamometry
Time Frame
12 weeks
Title
Change in peak oxygen uptake (VO2 peak)
Description
Cardiopulmonary exercise test will be performed to measure VO2 peak and other parameters representative of cardiovascular reserve.
Time Frame
12 weeks
Title
Microvascular reactivity
Description
A laser speckle contrast imaging system with a laser wavelength of 785 nm (PeriCam PSI system, Perimed, Järfälla, Sweden) coupled to iontophoresis of acetylcholine and sodium nitroprusside will measure non-invasively real time cutaneous microvascular flow changes in the forearm. For the post occlusive reactive hyperemia (PORH) test, arterial occlusion will be performed with suprasystolic pressure (50 mmHg above the systolic arterial pressure) using a sphygmomanometer applied to the arm of the subject over three minutes. Peak skin flow will be measured after pressure release.
Time Frame
12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Clinical diagnosis of heart failure NYHA I or II after medical evaluation;
Indication to participate in a cardiac rehabilitation program;
Fully medicated for heart disease;
Age greater than or equal to 50 years;
Ejection fraction less than 50%.
Exclusion Criteria:
Neoplasia at any site;
Impaired renal function (<50ml / min / 1.73m2);
Impaired hepatic function (TGP> 150U / l) or decompensated hepatic cirrhosis classified with Child-Pugh B or C;
Presence of ressincronizer or other device;
Atrial fibrilation;
Allergy of milk protein.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrea Lorenzo, PhD
Organizational Affiliation
National Institute of Cardiology, Laranjeiras, Brazil
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Annie SB Moreira, PhD
Organizational Affiliation
National Institute of Cardiology, Laranjeiras, Brazil
Official's Role
Study Director
Facility Information:
Facility Name
Elisa Maia dos Santos
City
Rio de Janeiro
ZIP/Postal Code
22240-006
Country
Brazil
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
All volunteer information obtained during the collection, intervention and data analysis will not be available other researchers.
Citations:
PubMed Identifier
30089525
Citation
Dos Santos EM, de Moraes R, Tibirica EV, Huguenin GVB, Moreira ASB, De Lorenzo AR. Whey protein supplementation for the preservation of mass and muscular strength of patients with heart failure: study protocol for a randomized controlled trial. Trials. 2018 Aug 8;19(1):431. doi: 10.1186/s13063-018-2811-4.
Results Reference
derived
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Effect of Whey Protein' Supplementation and Exercise in Patients With Heart Failure
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