Study to Evaluate Bioactive Peptides' Effect on Digestive Discomfort Symptoms of the Elderly (Inflammaging)

A Randomised, Double-blinded, Parallel Group, Placebo-Controlled Study to Evaluate the Effects of a Bioactive Peptide on Symptoms of Digestive Discomfort in the Elderly

This trial will investigate the potential of a bioactive peptide to reduce symptoms of digestive discomfort in a generally healthy elderly population. Participants will consume the bioactive peptide for 12 weeks and various measures indicating an improvement in health and well being will be taken throughout the trial. It is believed that consumption of the study product will reduce the severity of digestive discomfort, reduce chronic inflammation, improve blood glucose metabolism and improve physical performance.

Study Overview

• Status: Completed
• Conditions: Abdominal Pain
• Intervention / Treatment: Dietary supplement: Bioactive hydrolysate

Detailed Description

Forty subjects aged between 65 and 75 with self-reported symptoms of digestive discomfort will be randomised. Subjects will be randomised to receive either the Bioactive peptide or placebo for a total of 12 weeks.

Subjects will undergo an initial phone screen and will be asked questions regarding their age and their symptoms of digestive discomfort. Eligible subjects will be scheduled for a screening visit. The study will involve 5 visits over a 13 to 16 week period.

At the screening visit (Visit 1) the inclusion and exclusion criteria will be reviewed and the overall details of the study will be explained and informed consent obtained. Vitals and Medical history, demographic data and concomitant medication will be recorded.

Subjects will be asked questions relating to their digestive symptoms, including symptoms of abdominal pain, discomfort, bloating and flatulence. Subjects will complete the Digestive Symptom Frequency Questionnaire (DSFQ), the International Physical Activity Questionnaire (IPAQ) and the Mini-mental State Exam (MMSE) will be administered. The Fried Frailty score will be completed and the Short Physical Performance Battery (SPPB) test will be performed. A fasting blood sample (9mls) will be collected and haematology, biochemistry, glucose and blood lipids will be measured.

Subjects will be provided with a stool collection kit and instructions for collecting and storing. Subjects will collect a stool sample at home, within 24 hours of their next visit and bring it to the clinic at their next visit.

If the subject meets the eligibility criteria, they will be invited to participate in the study and will be given an appointment to return to the study site within 4 weeks for their baseline/week 0 visit.

Subjects will attend visit 2 fasting. The inclusion and exclusion criteria will be reviewed and eligibility for study entry confirmed. An Oral Glucose Tolerance Test will be performed. Haematology, biochemistry and blood lipids will also be measured.

A urine sample will be collected and also stored frozen for analysis of metabolites.

Vitals, anthropometric measurements, concomitant medication and any adverse events will be recorded and The Short Physical Performance Battery (SPPB) test will be performed.

Subjects will complete the Digestive Symptom Frequency Questionnaire and the hand-grip and chair-stand tests will be performed. A DEXA scan will be performed and muscle and fat mass recorded.

Subjects will be randomized to receive the Bioactive peptide or placebo and receive a 4 week supply of product and instructions for dosing. Subjects will be provided with a stool collection kit and instructions for collecting and storing. Subjects will collect a stool sample at home, within 24 hours of their next visit and bring it to the clinic at their next visit.

Subjects will return for visits at week 4, week 8 and week 12.

A similar regimen will be followed for visits at week 4, week 8 and week 12.

The site, investigator, protocol, informed consent form and any other pertinent documents for this study will be approved by: Cork Research Ethics Committee of the Cork Teaching Hospitals, Lancaster Hall, 6 Little Hanover Street, Cork.

The investigator is responsible for ensuring that all source documents (i.e. study and/or medical records) are completed and maintained according to the study protocol, Good Clinical Practice (GCP) and are available at the site.

LIST OF ABBREVIATIONS AND DEFINITION OF TERMS

ANCOVA Analysis of co-variance AUC Area Under the Plasma Concentration BMI Body mass index BP Blood pressure CI Confidence interval CRF Case Report Form CRO Contract Research Organization EFSA European Food Safety Authority GCP Good Clinical Practice GMP Good Manufacturing Practice HbAIc Glycated haemoglobin (A1c) ICH International Conference on Harmonization INCI The International Nomenclature of Cosmetic Ingredients ITT Intent-to-treat kDa Kilodalton kg Kilogram L Liter MCH Mean corpuscular hemoglobin MCHC Mean corpuscular hemoglobin concentration MCV Mean corpuscular volume MCPs Marine collagen peptides MedDRA Medical Dictionary for Regulatory Activities mITT Modified intention-to-treat mL Milliliter mmHg Millimeter of mercury mmol/mol Millimoles per mole OGTT Oral glucose tolerance test PPP Per protocol population RDW Red cell distribution width SAE Serious adverse event SAP Statistical analysis plan VLDL Very low-density lipoprotein WHO World Health Organisation

• Study Type: Interventional
• Enrollment (Actual): 40
• Phase: Not Applicable

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 65 years to 75 years (Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Be able to give written informed consent
• Be between 65 and 75 years of age (inclusive)
• Have symptoms of digestive pain & discomfort
• Have a Fried Frailty score of <2
• Have a Short physical performance battery (SPPB) score of >5 and <10
• Have a Mini Mental State Exam (MMSE) score >24
• Have low or moderate activity according to the IPAQ short form
• Have a BMI <30 kg/m2
• Be in good general health.

Exclusion Criteria:

• Are less than 65 and greater than 75 years of age
• Are severely immunocompromised (HIV positive, transplant Subject, on antirejection medications, on a steroid for >30 days.
• Have a diagnosis of Irritable Bowel Syndrome
• Is taking a high dose of statins and/or has changed had their dose modified in the previous 6 months
• Is experiencing muscle pain, soreness or muscle loss in the previous 6 months
• Has a history of drug and / or alcohol abuse at the time of enrolment
• Has changed their dietary habit within the preceding month
• Has a known organic disease, including an inflammatory bowel disease, a benign or malign tumour of intestine or colon and significant systemic disease
• Subject currently involved in any other clinical trial or having participated in a trial within the preceding 90 days
• Has known allergy to components of the test product
• Use of anti-inflammatory steroid medications, anticoagulants, current/recent (3 months) history of anabolic steroid, corticosteroid or estrogen use, testosterone replacement therapy (ingestion, injection, or transdermal), or any anabolic steroid
• Has any concurrent medical or psychiatric condition that, in the opinion of the Investigator, would compromise his/her ability to comply with the study requirements

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Prevention
• Allocation: Randomized
• Interventional Model: Parallel Assignment

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Bioactive hydrolysate; 20 g of hydrolysed rice protein	Dietary supplement: Bioactive hydrolysate; Participants given a bioactive vegetable hydrolysate to take one dose each morning and one dose each evening for the duration of the study.
Placebo Comparator: Placebo; 20 g micro crystalline cellulose	Dietary supplement: Bioactive hydrolysate; Participants given a bioactive vegetable hydrolysate to take one dose each morning and one dose each evening for the duration of the study.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Digestive symptom frequency questionnaire	The primary endpoint is the difference between the change experienced over 12 weeks in the active group versus the change in the placebo group using the digestive symptom frequency questionnaire (DSFQ) at baseline and end of treatment	Baseline (week 0) and end of treatment (week 12)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
To determine the effect of supplementation of a Bioactive Peptide on muscle mass	Muscle mass, measured by dual-energy x-ray absorptiometry (DXA) at weeks 0 and 12	Baseline (week 0) and week 12
To determine the effect of supplementation of a Bioactive Peptide on upper body muscle strength	Upper body muscle strength, measured by the hand-grip test	Baseline (weeks 0) and week 4, week 8 and week 12
To determine the effect of supplementation of a Bioactive Peptide on lower body muscle strength	Lower body muscle strength, measured by the chair stand test	Baseline (weeks 0) and week 4, week 8 and week 12
To determine the effect of supplementation of a Bioactive Peptide on physical performance	Short physical performance battery test score	Baseline (weeks 0) and week 12
To determine the effect of supplementation of a Bioactive Peptide on blood glucose	Glucose as measured by the Oral Glucose Tolerance Test	Baseline (weeks 0) and week 12
To determine the effect of supplementation of a Bioactive Peptide on blood markers of inflammation	Inflammatory cytokines (IL6 & IL1R, CRP, TNF)	Baseline (weeks 0) and week 4, week 8 and week 12
To determine the effect of supplementation of a Bioactive Peptide on blood lipid	Lipids (Total cholesterol, LDL, HDL, Triglycerides	Baseline (weeks 0) and week 4, week 8 and week 12

Collaborators and Investigators

• Sponsor: Nuritas Ltd
• Collaborators: Atlantia Food Clinical Trials

Study record dates

Study Major Dates

• Study Start (Actual): June 14, 2016
• Primary Completion (Actual): October 28, 2016
• Study Completion (Actual): January 20, 2017

Study Registration Dates

• First Submitted: June 25, 2020
• First Submitted That Met QC Criteria: June 25, 2020
• First Posted (Actual): June 30, 2020

Study Record Updates

• Last Update Posted (Actual): April 14, 2022
• Last Update Submitted That Met QC Criteria: April 6, 2022
• Last Verified: April 1, 2022

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pain; Neurologic Manifestations; Signs and Symptoms, Digestive; Abdominal Pain
• Other Study ID Numbers: AFCRO-063

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No