CHF COPD Sip Feed Anabolic Response

Pulmonary Disease, Chronic Obstructive Clinical Trial

Official title:

Anabolic Responsiveness to Protein Intake in Chronic Heart Failure and Chronic Obstructive Pulmonary Disorder

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02770092
• Other study ID #: IRB2015-0676
• Status: Recruiting
• Phase: N/A
• Start date: February 2016
• Est. completion date: February 2021

Study information

• Verified date: April 2019
• Source: Texas A&M University
• Contact: Marielle Engelen, PhD
• Phone: 9792202282
• Email: mpkj.engelen[@]ctral.org
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Weight loss commonly occurs in patients with chronic heart failure (CHF) and chronic obstructive pulmonary disorder (COPD), negatively influencing their quality of life, treatment response and survival. Loss of muscle protein is generally a central component of weight loss in CHF and COPD patients, but patients also have reductions in fat mass and bone density, independent of the severity of the disease state. The purpose of this study is to provide detailed insight in disease related gut function by obtaining information on gut permeability, digestion and absorption of glucose, fat and protein in CHF and COPD patients compared to matched healthy controls. This will provide required information that is necessary to implement new strategies to develop optimal nutritional regimen in CHF and COPD.

Description:

General aims:

• To study the whole-body protein anabolic effect of several dosages of a high-quality protein sip feeding in COPD and CHF subjects as compared to healthy controls.

• To investigate the anabolic threshold in subjects with COPD and CHF as compared to healthy controls.

Purpose and objectives: Although the Researchers' previous study supports the concept of supplementing high-quality milk proteins in chronic wasting diseases i.e., COPD and CHF, the dose-response anabolic effects of proteins with high EAA levels are still unclear. Furthermore, there is no insight in the actual protein requirements in COPD and CHF. The knowledge gained from this study will benefit insight in terms of promotion of protein gain after feeding in COPD and CHF subjects. Based on the obtained data of protein behavior (protein kinetics) the Researchers will be able to further refine and personalize nutritional supplementation in COPD and CHF subjects in order to stop and even restore progressive muscle wasting.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 150
• Est. completion date: February 2021
• Est. primary completion date: February 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 45 Years and older

Eligibility

Inclusion criteria CHF subjects:

• Ability to walk, sit down and stand up independently

• Age 45 years or older

• Ability to lie in supine or elevated position for 8 hours

• Diagnosis of CHF; under regular care by cardiologist

• Reduced ejection fraction (<45%) assessed in the past 2 years

• NYHA class II-IV

• Clinically stable condition; no hospitalization 4 weeks preceding first study day

• Willingness and ability to comply with the protocol

Inclusion criteria COPD subjects:

• Ability to walk, sit down and stand up independently

• Age 45 years or older

• Ability to lie in supine or elevated position for 8 hours

• Diagnosis of moderate to very severe chronic airflow limitation and compliant to the following criteria: FEV1 < 70% of reference FEV1

• Clinically stable condition and not suffering from a respiratory tract infection or exacerbation of their disease (defined as a combination of increased cough, sputum purulence, shortness of breath, systemic symptoms such as fever, and a decrease in FEV1 > 10% compared with values when clinically stable in the preceding year) at least 4 weeks prior to the first test day

• Shortness of breath on exertion

• Willingness and ability to comply with the protocol

Inclusion criteria healthy subjects:

• Healthy male or female according to the investigator's or appointed staff's judgment

• Ability to walk, sit down and stand up independently

• Age 45 years or older (older control group)

• Age between 20-30 years old (young group)

• Ability to lay in supine or elevated position for 8 hours

• No diagnosis of CHF or COPD

• Willingness and ability to comply with the protocol

Exclusion Criteria all subjects:

• Any condition that may interfere with the definition 'healthy subject' according to the investigator's judgment (healthy subjects only)

• Established diagnosis of malignancy

• History of untreated metabolic diseases including hepatic or renal disorder

• Presence of acute illness or metabolically unstable chronic illness

• Presence of fever within the last 3 days

• Body mass index >40 kg/m2 (healthy subjects only)

• Any other condition according to the PI or nurse that was found during the screening visit, that would interfere with the study or safety of the patient

• Use of protein or amino acid containing nutritional supplements within 5 days of first study day

• Current Use of long-term oral corticosteroids (CHF only)

• Use of short course of oral corticosteroids within 4 weeks preceding first study day

• Failure to give informed consent or Investigator's uncertainty about the willingness or ability of the subject to comply with the protocol requirements

• (Possible) pregnancy

• Already enrolled in another clinical trial and that clinical trial interferes with participating in this study

When during the period from enrollment to the test day any condition causing the subject to not meet inclusion criteria or to meet exclusion criteria, the subject will be excluded from the study.

Related Conditions & MeSH terms

• Chronic Disease
• Congestive Heart Failure
• Heart Failure
• Lung Diseases
• Pulmonary Disease, Chronic Obstructive

Intervention

Other:
• sip feeding with stable isotope infusion
such as glycerol, D2O, tyrosine, phenylalanine, glucose, arginine, and citrulline

Locations

Country	Name	City	State
United States	Texas A&M University-CTRAL	College Station	Texas

Sponsors (1)

Lead Sponsor	Collaborator
Texas A&M University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in net whole-body protein synthesis	Change in whole-body protein synthesis rate after intake of meal	0, 2, 5, 10, 15, 20, 30, 40, 50, 60, 90, 120, 150, 180, 210, 225, 240, 260, 280, 300, 320, 340, 360 ± 5 min
Secondary	Body Composition	Body composition as measured by Dual-Energy X-ray Absorptiometry	15 minutes on screening or study day 1
Secondary	Skeletal muscle strength	handgrip and kin-com 1-leg test	on study day 1
Secondary	Respiratory muscle strength	Maximum inhalation and exhalation pressure	on study day 1
Secondary	Gut function	Digestion of the stable tracers of amino acid	In postabsorptive and prandial state every 20 minutes up to 6 hours before each sip feeding on study day
Secondary	Group differences in state of mood as measured by the Hospital Anxiety and Depression Scale (HADS)	a fourteen item self-assessment scale. Seven of the items related to anxiety and seven relate to depression. Each item on the questionnaire is scored from 0-3 and this means that a person can score between 0 (no symptoms) and 21 (severe symptoms) for either anxiety or depression.	Postabsorptive state during 3 hours and change after feeding on study day 1
Secondary	Executive Function-Adolescent/Adult Sensory Profile (ASP):	a standardized self-questionnaire that generates an individualized profile of sensory processing across four quadrants: low registration, sensation seeking, sensory sensitivity, and sensation avoiding.	Postabsorptive state during 3 hours and change after feeding on study day 1
Secondary	Group differences in quality of life as measured by Short Form (36) Health Survey (SF36)	self administered questionnaire that measures each of the following eight health concepts: Physical Functioning (PF); Role-Physical (RP); Bodily Pain (BP); General Health (GH); Vitality (VT); Social Functioning (SF); Role-Emotional (RE); Mental Health (MH) as well as a reported Health Transition item (HT).	Postabsorptive state during 3 hours and change after feeding on study day 1
Secondary	Group differences in activity as measured by Physical Activity Scale for the Elderly (PASE)	questionnaire is intended for use in an elderly population and focuses on 3 types of activities: leisure time activities, household activities and work-related activities.	Postabsorptive state during 3 hours and change after feeding on study day 1
Secondary	Group differences in attention and executive functions as measured by Stroop Color-Word Test (SCWT),	a word page with words printed in black ink, a color page with blocks printed in color, and a color-word page where the color and the word do not match. The examinee reads the words or names the ink colors as quickly as possible within a time limit. Measures selective attention and inhibitory control. The total time in seconds was reported for each trial.	Postabsorptive state during 3 hours and change after feeding on study day 1
Secondary	Group differences in state of mood as measured by the Profile of Mood State (POMS)	A psychological distress scale to measure mood disturbance in 6 domains - fatigue-inertia, vigor-activity, tension-anxiety, depression-dejection, anger-hostility, and confusion-bewilderment. Healthy populations take 3 to 7 minutes to complete, and others may take up a bit longer.	Postabsorptive state during 3 hours and change after feeding on study day 1
Secondary	Group differences in learning and memory as measured by Controlled Oral Word Association Test (COWAT),	The examinee is required to say as many words as they can think of in one minute that begin with a given letter of the alphabet. The task contains three trials. Measures phonetic verbal fluency. The raw score (total and mean words recorded across the three trials) was reported.	Postabsorptive state during 3 hours and change after feeding on study day 1
Secondary	Group differences in learning and memory as measured by Auditory Verbal Learning Test (AVLT)	a verbal episodic memory test that evaluates a wide diversity of functions: short-term auditory-verbal memory, rate of learning, retention and recognition of information.	Postabsorptive state during 3 hours and change after feeding on study day 1
Secondary	Group differences in attention and executive functions as measured by PASAT	a measure of cognitive function that assesses auditory information processing speed and flexibility, as well as calculation ability.	Postabsorptive state during 3 hours and change after feeding on study day 1
Secondary	Group differences in attention and executive functions as measured by Trail Making Test (TMT)	n Part A, the examinee is instructed to connect a set of 25 circles with numbers as quickly as possible while maintaining accuracy. In Part B, the examinee is instructed to connect a set of 25 circles, alternating between numbers and letters, as quickly as possible while maintaining accuracy. Measures attentional resources and is a measure of the frontal lobe "executive" functions of visual search, set-switching and mental flexibility. The total time in seconds was reported for each measure.	Postabsorptive state during 3 hours and change after feeding on study day 1
Secondary	Group differences in overall cognitive abilities as measured by Montreal Cognitive Assessment (MoCA)	assesses several cognitive domains and is used for the screening of mild cognitive impairment. Total scores range from 0-30 with lower scores indicating decreased functioning.	Postabsorptive state during 3 hours and change after feeding on study day 1
Secondary	Group differences in attention and executive functions as measured by Brief-A	a standardized self-report that captures views of an adult's executive functions or self-regulation in his or her everyday environment.	Postabsorptive state during 3 hours and change after feeding on study day 1
Secondary	diet recall	The subject is asked to recall in detail all the food and drink consumed during the 24 hours prior to the test day.	on study day 1