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Pectin drink tested in older adults with early frailty

Recruiting · University of Nottingham

What this means

This is a planned trial that has not reported results yet. It will compare a pectin drink with a placebo drink taken daily for four weeks.

Plain-English summary written by an AI model from the registry listing.

Status
Recruiting
Who can join
Ages 65 and over
Where
1 site

Contacts and how to join ↗

The science

Registered title
The Effect of Pectin Supplementation on Geriatric With Frailty: A Randomised Placebo-Controlled Dietary Intervention Study
Phase
Not applicable
Study type
interventional
Conditions
Frailty at Older Adults, Pre-Frailty, Frailty, Diet, Dietary Fiber, Systemic Inflammatory Response
What is tested
Pectin, Whey protein
Sponsor
University of Nottingham
Ages
65 Years to no maximum
Dates
First posted May 2, 2025 · updated Jun 22, 2025

Registry summary

The study involves the intake of Low-methoxy (LM) pectin (polysaccharides extracted from citrus peels), which are commonly found in the UK diet (not pharmacological agents), to test their effects on systematic inflammation in the body and gut microbiome composition. Study subjects will be healthy elderly with early signs of frailty or pre-frailty from the local population and will be asked to attend the laboratory on 2 occasions; before and after 4-week' supplementing the diet daily with either 10g of pectin with 10g of whey protein and 10g of cocoa powder added as flavour (active arm) or 10g of whey protein with 10g of cocoa powder added as flavour (placebo). Participants will be given the blinded products portioned in individual sachets, with instructions to add the contents of one sachet a day to 150ml of milk and to consume immediately.

At each study visit (\~90 minutes), participants will be asked to provide a stool and blood sample, will have blood pressure, heart rate, weight, height, and waist/hip ratio measured, research team will perform physical functioning test (Time up and go test, 30-second sit to stand test) as well as participants will complete the quality-of-life questionnaire (SF-36), the Depression and Anxiety (HADS) and the Gastrointestinal Symptom Rating Scale (GSRS).

Sites (1)

  • University of Nottingham, Nottingham, Nottingham, United Kingdom
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