Skip to content

Galactooligosaccharide and Aging

Does Galactooligosaccharide Supplementation Improve Markers of Skeletal Muscle Health in Elderly Individuals?

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06411964
Enrollment
30
Registered
2024-05-14
Start date
2024-05-02
Completion date
2025-10-06
Last updated
2024-05-16

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

Conditions

Muscle Loss

Keywords

sarcopenia, physical function, aging, gut microbiome, prebiotic

Brief summary

Sarcopenia is a progressive muscle disease, most commonly affecting older individuals, that is categorised by 1) low muscle strength, 2) low muscle quantity or quality, and 3) low physical performance. This disease has several negative implications for human health, including an increased risk of falls, fractures, mobility limitations, and mortality. Sarcopenia also imposes significant burden on healthcare systems. For example, it was estimated that a 10% reduction in the prevalence of sarcopenia would save the US healthcare system $1.1 billion per year. Strategies to reduce the incidence and severity of sarcopenia are therefore of great interest. One potential cause for sarcopenia is long-term, low-level inflammation, which can occur for a number of reasons. One cause may relate to the intestinal wall becoming more susceptible to leaking of toxic particles. Evidence suggests that prebiotic supplementation can reduce this 'leakage'. Galactooligosaccharide (a prebiotic) has previously been shown to reduce inflammation in elderly individuals. The investigators hypothesise that galactooligosaccharide will improve physical function in the elderly indirectly via a reduction in inflammation. This will be a randomised, placebo-controlled, double-blind, parallel study. 32 elderly individuals (65-85 years; mix of males and females) will be randomised to one of two groups, GOS or PLACEBO. The GOS group will supplement their diet with 2.9 g galactooligosaccharide per day for 16 weeks in the form of one sachet (3.65 g) of Bimuno® Daily. The PLACEBO group will supplement with 3.65 g maltodextrin per day for 16 weeks. The study will involve one screening visit and two main trials (baseline and 16 weeks). For the main trials, participants will complete the short physical performance battery (SPPB) and handgrip strength test. In addition, participants will provide blood, urine and faecal samples, as well as a dual-energy x-ray absorptiometry (DEXA), and a peripheral quantitative computed tomography (pQCT) scan.

Interventions

DIETARY_SUPPLEMENTPlacebo control

maltodextrin control supplement

DIETARY_SUPPLEMENTPrebiotic

Commercially available supplement (Bimuno)

Sponsors

University of Bath
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Masking description

double blind

Eligibility

Sex/Gender
ALL
Age
65 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged 65-85 years * Able to rise from a chair without using arms

Exclusion criteria

* Use of products marketed as prebiotics, probiotics or synbiotics within 4 weeks prior to study entry (e.g., Yakult, Actimel, Activia, VSL#3, Kefir). Regular cheese or yogurt containing lactic acid bacteria are not an exclusion criterion * Systemic antibiotic or antimycotic treatment 6 weeks prior to study entry. * Following diets likely to affect study outcomes: e.g., low FODMAP, KETO/high-fat, gluten free/coeliac, paleo, weight loss, caloric restriction, low-carb, 5:2/whole day energy restriction, Atkins/high-protein, sugar-free, single-food, juicing/any day of juicing, any other restriction diet (e.g. very low calorie), or vegan diets (GOS is derived from cow's milk) * Meeting physical activity guidelines for older adults: * Activities that improve strength, flexibility and balance at least two days per week * At least 150 minutes of moderate-intensity activity, or 75 minutes of vigorous activity * Body mass loss of ≥ 5% in preceding 6 months * History of injury or surgery that would affect physical ability to undertake physical tests * History of gastrointestinal disease (e.g., inflammatory bowel disease, irritable bowel syndrome)

Design outcomes

Primary

MeasureTime frameDescription
Mid-thigh muscle cross sectional area16 weekspQCT assessment of mid-thigh cross sectional area

Secondary

MeasureTime frameDescription
Short performance physical battery16 weekscomposite test of balance, gait speed and chair stand tests where performance on each three tests scores of maximum of 4 points, combined to score a maximum of 12 points
Handgrip strength16 weeksdominant and non-dominant hand scores
appendicular lean mass/height^2 (kilograms/metres^2)16 weeksassessed via DEXA scan
gait speed16 weeks4m gait speed at usual walking pace (metres/second)
chair stand16 weeks5 time chair stand (seconds)

Countries

United Kingdom

Contacts

Primary ContactAdam J Collins
ac3413@bath.ac.uk07710611694
Backup ContactJavier T Gonzalez
jg833@bath.ac.uk01225385518

Outcome results

None listed

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