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Investigating the Glycaemic and Satiating Capacity of PulseOn® Enriched Foods

Investigating the Glycaemic and Satiating Capacity of PulseOn® Enriched Foods: a Randomised Control Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06508424
Enrollment
50
Registered
2024-07-18
Start date
2024-07-31
Completion date
2024-11-30
Last updated
2024-07-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Appetitive Behavior, Energy Intake, Glycaemic Response

Brief summary

The purpose of this randomised control trial is to determine whether consuming PulseOn enriched crackers for breakfast influences post-prandial glycaemic response and markers of appetite (hunger, fullness, desire to eat) over 4 hours, and energy intake at an ad libitum lunch meal on the same day. Healthy individuals with no underlying metabolic disease will be recruited to take part in this study.

Detailed description

PulseON® is a unique flour that is made 100% from pulses, but unlike other flours it has been obtained through an alternative milling process (WO2019155190) which preserves whole plant cells (Edwards et al., 2020). These cells were shown to remain intact during down-stream processing into food products including bread and biscuits, and influence glycaemic response to these foods (Delamare et al., 2020; Bajka et al., 2021). Interestingly, the PulseON®-enriched breads also significantly enhanced and prolonged release of the gut hormones glucagon-like peptide-1 (GLP1) and peptide YY (PYY), which are known to have anorexigenic effects (Bajka et al., 2023). Studies using chick pea purees and hummus products have also shown positive findings in relation to appetite sensations and food intake (Pälchen et al., 2022; Alshaalan et al., 2024). This work aims to recruit 50 participants through the use of posters and emails at Sheffield Hallam University, as well as in the local Sheffield area and through social media. -30 minutes - baseline measures (body mass index (kg/m2), waist circumference (cm), blood glucose (mmol/l), hunger, fullness, desire to eat) are taken 0 minutes - pre-load consumed within 15 minutes (75g wheat flour / PulseOn crackers) The wheat flour cracker is made from 100% wheat flour. The PulseOn cracker is made from 40% PulseOn flour and 60% wheat flour. 30, 45, 60, 75, 90, 105, 120, 150, 180, 210 minutes - repeat baseline measures 240 minutes - ad libitum lunch provided (pasta and tomato sauce) and participants instructed to eat to fullness. Paired sample t-tests will be used to compare measures between the two visits.

Interventions

OTHERPulseOn

PulseOn - 1 week washout period between interventions 75g crackers

OTHERWheat flour control

Control -1 week washout period between interventions 75g crackers

Sponsors

Quadram Institute Bioscience
CollaboratorOTHER
Biotechnology and Biological Sciences Research Council
CollaboratorOTHER
Sheffield Hallam University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Masking description

Participants will not be told which arm of the trial they are taking part in. PulseOn crackers and the wheat flour control crackers have been matched as closely as possible for energy content and sensory characteristics. Participants will be asked to rate the acceptability of the crackers to determine whether there are any discernible differences, however they are required to consume a set amount.

Intervention model description

Participants will be randomly assigned to either the treatment (PulseOn) or control group at the outset of their participation. Following a minimum of a one-week washout period, participants will then participate in the alternative arm.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* over the age of 18y

Exclusion criteria

* smoker / recreational drug user * restrained eater (as determined by the three factor eating questionnaire (TFEQ-R18)) * vegan * pregnant / lactating * blood clotting disorder * taking medication for heart / metabolic disease * pacemaker fitted * energy restricted diet or lost \>5% body weight in the last 3 months * elite athletes * dysphagia * food allergy / intolerance * disease / inflammation of the GI tract

Design outcomes

Primary

MeasureTime frameDescription
Energy Intake at a test mealParticipants consume the preload at 0 minutes, and the test meal at 240mins.Following the consumption of either the control / PulseOn enriched preload (crackers), participants will be asked to consume a standardised lunch meal of pasta and tomato sauce until they are full. The amount consumed will be measured using the Sussex Ingestion Pattern Monitor, and reported in grams and kcals.
Glycaemic responseBaseline blood measures to be taken at -30 minutes. Participants consume the preload at 0 minutes, and capillary blood samples are measured at 30, 45, 60, 75, 90, 105, 120, 150, 180 and 210 minutes.Following the consumption of either the control / PulseOn enriched preload (crackers), capillary blood samples will be measured at 15 / 30 minute intervals up to lunch time.
Markers of appetiteBaseline hunger, fullness and desire to eat to be taken at -30 minutes. Participants consume the preload at 0 minutes, and further hunger, fullness and desire to eat measures are taken at 30, 45, 60, 75, 90, 105, 120, 150, 180 and 210 minutes.Following the consumption of either the control / PulseOn enriched preload (crackers), hunger, fullness and desire to eat will be measured at 15 / 30 minute intervals up to lunch time using visual analogue scale.

Secondary

MeasureTime frameDescription
MoodBaseline mood ratings will be measured at -30 minutes. Participants consume the preload at 0 minutes, and further mood ratings are measured at 30, 45, 60, 75, 90, 105, 120, 150, 180 and 210 minutes.Following the consumption of either the control / PulseOn enriched preload (crackers), the following attributes will be measured at 15 / 30 minute intervals up to lunch time using visual analogue scale - happy, relaxed, energetic, thirsty, nauseous.
Post intervention food / energy / nutrient intake24hrs post interventionFollowing the completion of the lab-based study, participants will leave the research facility and complete a 24hr estimated measures diet diary which will be analysed on Nutritics.

Countries

United Kingdom

Contacts

Primary ContactAnna C Sorsby, MSc
a.sorsby@shu.ac.uk01142256279
Backup ContactCaroline E Millman, PhD
c.e.millman@shu.ac.uk01142256871

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026